Patent Application
20160298112
The present invention concerns the use of particular RNA sequences as a medicament. More precisely, it concerns the use of small nucleolar RNAs (snoRNAs) which inventors have shown to be involved in the mechanisms of aging. The snoRNAs of the invention can be used in particular to increase the stress resistance of a subject, to fight against the harmful effects of aging, typically for preventing or treating a degenerative disease, in particular neurodegenerative, a laminopathy, in particular Hutchinson-Gilford syndrome (HGPS) (also known as progeria), diabetes, obesity or a cancer and, more generally, to prolong the lifespan of a subject. The snoRNAs of the invention can also be used in the treatment of infertility.
The invention further relates to vectors, cells, transgenic animals and compositions capable of expressing a snoRNA of the invention, and methods using any of the above products of the invention as a tool for identification of a molecule active in the prevention or treatment of a pathology, abnormality, disorder or an apparent or functional deterioration linked to a mechanism of aging.
The mechanisms of aging (i.e., progressive decline in the capacity to survive and reproduce with age) have perplexed society and the scientific community for centuries. There are two currently prevailing theories, one that aging results from a genetically preprogrammed evolutionary path and the other that aging is a normal consequence of existence during which cellular and molecular damage accumulates. This damage would include oxidative damages induced by free radicals, defective mitochondria, somatic mutations, progressive shortening of telomers, programmed cell death and proliferation of damaged cells, etc. (Semsei I. (2000) On the nature of aging. Mech Aging Dev 117:93-108).
It has been shown, in organisms like yeast and mice, that caloric reduction exerts a decisive positive impact on lifespan extension (Sohal, R S, Weindruch, R (1998) Oxidative stress, caloric restriction, and aging. Science 273:59-63; Finch, C E, Revkun, G. (2001) The genetics of aging. Annu. Rev. Genom. Hum. Genet. 2:435-462). Recent studies have shown that caloric restriction would also be effective in primates, including humans (Roth, G S, Lasnikov, V, Lesnikov, M, Ingram, D K, Land, M A (2001) Dietary caloric restriction prevents the age-related decline in plasma melatonin levels of rhesus monkeys. J Clin Endocrinol Metab. 86: 3292-5; Roth G S, Lane M A, Ingramn D K, Mattison J A, Elahi D, Tobin J D, Muller D, Metter E J (2002) Biomarkers of caloric restriction may predict longevity in humans. Science. 297: 811-813; Walford R L, Mock D, Verdery R, MacCallum T. (2002) Calorie restriction in biosphere 2: alterations in physiologic, hematologic, hormonal, and biochemical parameters in humane restricted for a 2-year period. J Gerontol A Biol Sci Med Sci 57: 211-24). Unfortunately, it is probable that the majority of humans are not capable of following the strict diet required to benefit from this discovery.
For several years, many research groups have been dedicated to identifying the genes and signalling pathways involved in the aging process. The studies reported here are conducted in numerous organisms, including yeast Saccharomyces cerevisiae, worm Caenorhabditis elegans and fly Drosophila melanogaster (Fontana et al., 2010), and permitted identifying a growing list of genes. Many of them are involved in hormone signalling and are conserved in a large variety of eukaryotic organisms. It has become clear that, at least for lower species, the pathways responsible for development and growth at the start of life retain a lifelong influence and even partially condition its duration. These studies have also indirectly shown the importance of metabolic capacity and stress resistance for evaluating the lifespan of a subject.
For example, mutants of the clk-1 gene of Caenorhabditis elegans were involved in reducing the extra-mitochondrial production of reactive oxygen species (Hekimi, S, Guarente, L. (2003) Genetics and the specificity of the aging process. Science 299:1351-1354). Patent WO 98/17823 describes the function of the clk-1 gene in the processes of development and longevity. It particularly claims a method to increase an individual's lifespan by regulation of clk-1 gene expression.
A mutation of the Methuselah gene (which codes for a G-protein coupled receptor) has also been described as capable of increasing the lifespan of Drosophila by around 35% (U.S. Pat. No. 6,303,768). Telomer shortening is also known as a mechanism responsible for cell aging. In vertebrates, telomerase is a ribonucleoprotein (RNP) reverse transcriptase whose role is to maintain the length of telomers by addition of telomeric DNA to the end of chromosomes in dividing eukaryotic cells (Kiss, 2002). In humans, a mutation in the H/ACA box of telomerase snoRNA causes a pleiotropic genetic disease, dyskeratosis congenita, whose patients present shorter telomers (Mitchell et al., 1999; Vulliamy et al., 2001). Despite the efforts of the scientific community to decode the mechanisms of aging and identify new therapeutic targets to delay this process and/or combat its harmful effects, the tools available remain insufficient. The need for tools that permit “aging well”, that is without the diseases and discomforts generally associated with old age, is felt all the more now that medical progress combined with general improvement in life conditions have already permitted the human population, in just a few decades, to increase its life expectancy in a very significant manner.
The present invention relates to the prophylactic or therapeutic use of the RNA sequences of interest for which the inventors have demonstrated particular involvement in the mechanisms of aging. They have especially shown the ability of these sequences to spectacularly increase the lifespan of a subject by stopping the mechanisms of aging and fighting the harmful effects associated therewith. The sequences of the invention also fight diseases associated with aging such as degenerative diseases, laminopathies and cancers, as well as diabetes and obesity. They have proven especially effective in the treatment of infertility or sterility (i.e., difficulty conceiving or inability to conceive) as well as increasing the resistance of subjects, in particular subjects who have reached sexual maturity, preferably elderly subjects, to stress.
A first subject of the invention relates to an isolated or synthetic RNA sequence comprising sequence SEQ ID NO: 1, a homologous sequence, preferably an orthologous sequence, or a functionally analogous sequence, for use as a medicament.
The inventors have demonstrated that the RNA sequence SEQ ID NO: 1 discovered in Drosophila corresponds to orthologous sequences in mammals such as primates and human being, and in rodents such as mice and rats. The invention also covers the use, in one or the other of the applications described in this text, of an isolated or synthetic RNA sequence preferably chosen from among sequence SEQ ID NO: 2 of human origin and sequences SEQ ID NO: 3 and SEQ ID NO: 4 of mouse origin. Sequences SEQ ID NO: 2, 3, 4, 9, 11, 13, 15, 17, 19, 21, 22, 24, 26, and 28 identified in Table 1 of this text are examples of sequences orthologous to SEQ ID NO: 1.
Another subject of the invention is a DNA sequence coding for a RNA sequence of interest according to the invention.
The invention also concerns a vector permitting in vitro, ex vivo or in vivo expression of a RNA sequence according to the invention.
The invention also concerns a cell comprising a RNA sequence according to the invention or transformed by a vector according to the invention, as well as a composition comprising a product according to the invention and a dietarily- or pharmaceutically-acceptable support.
The invention also concerns the use of a RNA sequence, vector, cell or a composition according to the invention, continuously or sequentially, to restore or modulate the expression of said RNA sequence in vivo, in vitro or ex vivo.
Another object of the invention is a transgenic mouse whose genome has been genetically modified to prevent or modify, preferably alter, the expression of a RNA sequence of interest according to the invention, typically one and/or the other of sequences SEQ ID NO: 3 and SEQ ID NO: 4.
The invention also covers a method for evaluating the cosmetic or therapeutic efficacy of a test compound to fight the harmful effects of aging or stress, or to fight infertility, said method comprising i) exposure of a cell or population of cells not expressing the RNA sequence of the invention or expressing an abnormal version of said RNA sequence; or a transgenic mouse according to the invention, ii) evaluation of the effects, if any, of the test compound on the phenotype of said cell(s) or said transgenic mouse, and iii) determination of the cosmetic or therapeutic efficacy of said test compound, a restoration of the activity and/or expression of said RNA sequence being correlated with efficacy of said test compound.
The invention also covers a method for evaluating the cosmetic or therapeutic efficacy of a test compound to fight the harmful effects of aging or stress, or to fight infertility, said method comprising i) exposure of a cell according to the invention comprising an RNA sequence according to the invention or a population of cells comprising a cell according to the invention; ii) evaluation of the effects, if any, of the test compound on the phenotype of said cell or population of cells, and iii) determination of the cosmetic or therapeutic efficacy of said test compound, an increase of the activity and/or expression of said RNA sequence being correlated with efficacy of said test compound.
The invention also concerns kits comprising nucleic acids, vectors, cassettes and/or cells such as described previously.
The invention results from the demonstration by the inventors of the influence of a small sequence of nucleolar DNA (snoRNA:Ψ28S-1153 called “youth”, identified in this text as SEQ ID NO: 1) on the lifespan of Drosophila. This snoRNA has been identified as part of a systematic screening of snoRNAs associated with the Drosophila genome (Huang et al., 2005) without any function being ascribed to it to date.
The inventors have characterized this sequence and notably shown that a genomic deletion of 632 base pairs of the F4 region of the Drosophila genome containing the snoRNA:Ψ28S-1153, shortens the lifespan of Drosophila by around 30%. They then demonstrated that the over-expression of this RNA sequence, for example using a transgene containing genomic DNA coding for this snoRNA, spectacularly increases the lifespan of Drosophila by around 100%. Flies overexpressing the RNA sequence of the invention live up to twice as long. Furthermore, the inventors have identified and detected the expression of orthologous “youth” sequences in mice and humans.
As explained previously, the invention concerns an isolated or synthetic ribonucleotide sequence (RNA sequence) with the functional characteristics of sequence SEQ ID NO: 1 identified originally in Drosophila (Drosophila melanogaster), for use as a medicament in a subject who can benefit from it, typically an animal or insect, for example a mammal or a rodent, preferably a human being.
“Medicament” means a substance possessing preventive or curative properties. In the context of the invention, a medicament is intended to cure, promote cure, relieve or prevent, in a subject as defined previously, a pathology, abnormality or impairment related to an abnormal or simply undesirable aging process.
In Drosophila, the RNA sequence of interest is comprised in the genomic region identified as region F4, itself located on chromosome 2R. This nucleotide sequence is, for the first species of Drosophila (Drosophila melanogaster) studied by the inventors, constituted of 148 base pairs. It is identified in this text as SEQ ID NO: 1.
Homologs/orthologs as well as functional analogs and variants of sequence SEQ ID NO: 1 are, likewise, sequences of interest that are objects of the present invention.
The term “homolog” is used in the context of the present invention to designate a structure whose nucleotide sequence is identical or sufficiently close to that of sequence SEQ ID NO: 1, identified in this first species of Drosophila, to be considered as its equivalent in another species (Drosophila, insect, or any other animal). A sequence is considered as a homolog of sequence SEQ ID NO: 1 if it has therewith, or with a fragment thereof of at least 50 consecutive nucleotides, a sequence identity of at least 70%, 80% or 85%, preferably at least 90 or 95%, more preferably at least 96, 97, 98 or 99% obtained, for example, by the blastN sequence alignment program (Altschul et al., 1990), or by the INFERNAL program for “INFERence of RNA ALignment”, which identifies DNA sequences from RNA structure and their sequence similarity. Two homologous genetic sequences of two different species are considered orthologs if they descend from a unique sequence present in the last common ancestor of the two species.
The percentage of identify is determined by comparing two sequences for which an optimal alignment has been done. The percentage of identity is calculated by determining the number of positions for which an identical residue appears over both sequences at the same position divided by the total number of positions and multiplied by 100. The optimal alignment of the two sequences can be obtained, for example, with a local homology search algorithm (Smith & Watherman, 1981) or equivalent systems known to the person skilled in the art.
The term “analog” designates any mimetic that is a chemical compound existing in nature and isolated therefrom, or produced artificially, and which has at least one of the endogenous functions of the nucleotide sequence that it imitates (functionally-equivalent RNA sequence), for example all the endogenous functions of the nucleotide sequence which it imitates. An example of an analog compound consists, for example, in a sequence permitting splicing the same genes. A particular object of the invention therefore concerns a sequence analogous to SEQ ID NO: 1 that permits splicing one or more genes chosen from among Ir56d, buttonhead, klarsicht, CG3262, CG30502 (fatty acid 2-hydroylase-fa2h), CG11125, CG9339, and CG40006 of Drosophila melanogaster. Experiments conducted by the inventors have demonstrated, for example, that gene CG9339 (called skywalker) (Uytterhoeven et al., 2011) is not correctly spliced in the F4 mutant, indicating that the youth snoRNA is involved in the alternative splicing of this gene (see
The term “functional variant” means any nucleic acid having one or more modifications or mutation (i.e., for example, a deletion, substitution or addition of one or more bases) relative to parent sequences described in this application, and permitting the applications described in the context of the present invention.
A sequence considered to be a homolog, preferably an ortholog, of a reference sequence in the sense of the invention is an example of a functional variant in the sense of the invention of said reference sequence. Such a sequence can be natural, recombinant or synthetic.
Sequence SEQ ID NO: 1 is a highly conserved sequence throughout evolution and present in many animal species. The inventors have therefore notably shown that this sequence is present in the 12 other species of Drosophila whose genome is known. Examples of sequences homologous/orthologous to RNA sequence SEQ ID NO: 1 therefore also comprise RNA sequences SEQ ID NO: 9, 11, 13, 15, 17, 19, 21, 22, 24, 26, and 28 identified in Table 1 of this text (see
The inventors have also identified an orthologous RNA sequence in the human being, located on chromosome 11, in position 12822722-12822811. It is the sequence identified in this text as SEQ ID NO: 2. The inventors have also identified two orthologous RNA sequences in mice (these are the sequences identified, respectively, as SEQ ID NO: 3 and 4 in this text), located on chromosome 15, in position 30336889-30337017 (SEQ ID NO: 7) and on chromosome 18, in position 6495012-6495091 (SEQ ID NO: 8).
Nucleotide sequences of interest identified in Drosophila, humans and mice are listed in Table 1 below.
Drosophila
melanogaster
Drosophila
Drosophila
sechellia
Drosophila
yakuba
Drosophila
erecta
Drosophila
ananassae
Drosophila
pseudoobscura
Drosophila
persimilis
Drosophila
willistoni
Drosophila
mojavensis
Drosophila
virilis
Drosophila
grimshawi
Drosophila
melanogaster
Drosophila
simulans
Drosophila
sechellia
Drosophila
yakuba
Drosophila
erecta
Drosophila
ananassae
Drosophila
pseudoobscura
Drosophila
persimilis
Drosophila
willistoni
Drosophila
mojavensis
Drosophila
virilis
Drosophila
grimshawi
One particular subject of the invention concerns the use of RNA sequence SEQ ID NO: 1 to identify a target gene, characterized in that said sequence SEQ ID NO: 1 is capable of recognizing a target sequence within a Drosophila melanogaster gene preferably chosen from among Ir56d, buttonhead, klarsicht, CG3262, CG30502 (fatty acid 2-hydroylase: fa2h) and CG11125, CG9339, CG40006, said target sequence being preferably chosen from among SEQ ID NO: 31 (TGGTTGAATTCACAAAA), SEQ ID NO: 32 (TTGAATTCACAAAATA), SEQ ID NO: 33 (AATTCACAAAATAGGC), SEQ ID NO: 34 (AAGCGTTAGATATTAA), SEQ ID NO: 35 (ACATCTGCGGATAAGA), SEQ ID NO: 36 (AAGCTTTGCGTTTTGA), and SEQ ID NO: 37 (AGAAGCTTTGCGTTTT), or an analogous sequence thereof.
In the context of the present invention, the RNA sequences of interest are preferably in the form of snoRNAs. In the context of the invention, the term “snoRNAs” encompasses a group of non-coding RNAs present in all eukaryotic cells. They are located in the nucleus and more particularly in the nucleolus where they are associated with proteins with which they form small nucleolar ribonucleoproteins or snoRNPs. They are generally produced from pre-mRNA introns. On the evolutionary scale, these non-coding RNAs are present from archaea to mammals. snoRNAs can have several functions, such as modification of ribosomal RNA, like 2′-O-ribose methylation or pseudouridylation of various classes of RNA. They have been involved in the nucleolytic process of ribosomal RNAs or even in the synthesis of telomeric DNA (Kiss, 2002; Kiss et al., 2010; Ye, 2007). There are two main classes of snoRNAs: the one comprising a C/D box and the one comprising an H/ACA box (
The snoRNA:Ψ28S-1153 (youth) of interest, identified in a first species of Drosophila, belongs to the H/ACA class, that is, its structure comprises an H/ACA box. It would therefore be involved in pseudouridylation (i.e., the conversion of uridine into pseudouridine) during the maturation of ribosomal RNA, and would regulate the protein synthesis of certain genes.
The snoRNAs according to the invention can be chemically modified, typically to increase the resistance of the snoRNAs to nucleases, to confer a better affinity/selectivity and therefore a better functionality of the snoRNAs. The modifications typically concern a nucleoside or internucleoside link. They can concern the sugar, for example (typically the 2′ position of the sugar), the nitrogenous base of the nucleoside (which typically comprises a substituent in position 2, 4 or 6) or one (or more) phosphate groups.
The modification may consist, for example, in an amination, halogenation, for example fluoridation, or alkylation, for example methylation. A modified sugar group can therefore be chosen, for example, from among the 2′-O-methyl and 2′-O-methoxyethyl groups.
A modified nucleotide can be a nucleotide comprising a heterocyclic base incapable of creating hydrogen bonds with heterocyclic DNA or RNA bases.
The modification of the internucleoside link is, for example, chosen from among a phosphorothioate, methylphosphonate, phosphotriester, phosphorodithioate and phosphoselenate bond.
The present invention also concerns the deoxyribonucleotide sequences (DNA) responsible for the expression of the RNA sequences of interest of the invention. The DNA sequence permitting the expression of RNA sequence SEQ ID NO: 1 is the sequence identified in the present invention as SEQ ID NO: 5, the one permitting the expression of sequence SEQ ID NO: 2 is the sequence identified in the present invention as SEQ ID NO: 6, the one permitting the expression of sequence SEQ ID NO: 3 is the sequence identified in the present invention as SEQ ID NO: 7, and the one permitting the expression of sequence SEQ ID NO: 4 is the sequence identified in the present invention as SEQ ID NO: 8.
One object of the invention therefore also concerns an isolated or synthetic DNA sequence selected in the group comprising SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, and SEQ ID NO: 30, and characterized in that it permits the expression of an RNA sequence of interest according to the invention.
Like the snoRNAs, the DNAs according to the invention can be modified chemically (see the chemical modifications possible above).
The invention also concerns any recombinant expression cassette, characterized in that it comprises a nucleic acid sequence of interest according to the invention such as defined in this text. The term expression cassette designates a nucleic acid construct/construction comprising a nucleic acid sequence permitting the expression of an RNA sequence of interest according to the invention and a regulator region, operably linked. The expression “operably linked” indicates that the components are combined so that the expression of the nucleic acid sequence (responsible for the expression of the RNA sequence of interest) and/or the targeting of the RNA sequence of interest are under control of the transcriptional promoter. Typically, the promotor sequence is placed upstream of the nucleic acid sequence, at a distance from the latter compatible with expression control. Spacer sequences can be present, between the regulator elements and the coding sequence, as long as they do not impede the expression and/or targeting of the RNA sequence of interest.
Another object of the invention concerns any (expression) vector comprising a nucleic acid or a cassette such as previously defined permitting the expression of a RNA sequence of interest according to the invention in a host cell or a host organism. The vector can be a DNA or RNA, circular or otherwise, single or double strand. It is typically a plasmid, phage, viral vector (chosen, for example, from among an adenoviral vector, a retroviral vector, an adenovirus-associated vector, a lentiviral vector, a poxvirus vector, a herpetic vector, etc.), a cosmid or an artificial chromosome. Advantageously, it is a vector capable of transforming a eukaryotic cell, preferably an animal cell, typically a human cell, preferably a cell of intestinal or ovarian origin. Such vectors are well known to the person skilled in the art and are particularly described in patent application WO 06/085016 or in the articles by Barton and Medzhitov, 2002; Tiscornia et al., 2004; Xia et al., 2002 et Shen et al., 2003.
One preferred vector permitting the expression of a RNA sequence of interest according to the invention can be chosen from among, for example, a plasmid, a cosmid, a viral vector or a phage. One preferred vector usable in particular in Drosophila is the pChs-Ga14 vector, in which is inserted, upstream of the Ga14 transcription factor, a specific DNA sequence, known to regulate the expression of a given gene in a given tissue, such as for example MyolA-Ga14, snail-Ga14, Su (H)-GBE-Ga14, Delta-Ga14. Simultaneously, a second vector (pUAs-snoRNA) comprising the effector gene of interest, here the snoRNA, is preferably positioned downstream of the UAS (Upstream Activating Sequence) regulatory sequences, these latter being recognized by the P[GAL4] transcription factor. Each of these two vectors is then introduced by transgenesis into an animal. These two animal lines are then crossed. This system is called: P[GAL4] binary expression system (Brand and Perrimon, 1993; Elliott and Brand, 2008). Therefore, more specifically, the MyolA-Ga14, snail-Ga14, Su(H)-GBE-Ga14 and Delta-Ga14 vectors comprise a promotor and regulator elements promoting the expression of said RNA sequence in intestinal cells, while the nanos-Ga14, or MTD-(maternal-Tubulin)-Ga14 vectors comprise a promotor and regulator elements promoting expression of said RNA sequence in the ovaries.
The vectors of the invention can also comprise an origin of replication, a selection gene, a reporter gene and/or a recombination sequence, etc. The vectors can be constructed by standard molecular biology techniques, well known to the person skilled in the art, using, for example, restriction, ligation, cloning, replication, etc. enzymes. Specific examples of vectors in the sense of the invention are provided in the experimental part. These vectors may include, for example, the P[GAL4] binary system (mentioned above) (Brand and Perrimon, 1993; Elliott and Brand, 2008).
The invention also concerns a cell comprising an RNA sequence according to the invention or transformed by means of a construct or vector according to the invention. The cell is preferably an intestinal or ovarian cell. Even more preferred, it is an intestinal stem cell, an enteroblast, an enterocyte, an entero-endocrine cell, a nurse cell or an oocyte.
The invention also comprises the use of a product according to the invention, typically a RNA sequence, a DNA sequence, a vector or a cell according to the invention, continuously or sequentially, to restore or modulate, typically amplify, in vitro, ex vivo or in vivo, the expression of the RNA sequence of interest according to the invention.
The invention also concerns a transgenic mouse whose genome (typically SEQ ID NO: 7 or SEQ ID NO: 8) has been genetically modified, using techniques well known to the skilled person, to prevent or modify, for example increase or decrease, expression, preferably alter expression of one or the other of SEQ ID NO: 3 and SEQ ID NO: 4.
The mouse is advantageously genetically modified by homologous recombination (knock-in, knock-out, knock-down) techniques known to the skilled person, including, for example, the use of the CRE/LOX system.
The invention also concerns compositions comprising an RNA sequence, a DNA sequence, a construct, a vector or a cell according to the invention.
The RNA sequences of the invention are very stable and very resistant in vitro. However, in the case of an administration to a subject to be treated, the compositions according to the invention may also advantageously comprise a dietarily- or pharmaceutically-acceptable support.
The expression “dietarily-acceptable support” designates a carrier permitting the subject to ingest and digest without risk the composition comprising a RNA sequence, a construct, a vector or a cell according to the invention comprising such a sequence, and capable of protecting said sequence from any attack, in particular related to food digestion, that could alter it before it produces its therapeutic action.
The expression “pharmaceutically-acceptable support” designates a carrier permitting risk-free administration of the composition comprising a RNA sequence, a construct, a vector or a cell according to the invention comprising such a sequence, according to one of the possible administration routes described below.
Advantageously, the carrier of the present composition facilitates penetration of the RNA of interest, the construct or the expression vector according to the invention into cells, ideally into particular cells as identified in this text, of the subject being treated, and/or protects the RNA, the construct or the expression vector from any damage that may impair its efficacy.
The choice of carrier as well as the content of active substance in the carrier are generally determined relative to the solubility and chemical properties of the active substance, the mode of administration and the characteristics of the subject to be treated.
Usable carriers or supports, acceptable pharmaceutically, include natural cationic polymers such as chitosan or atelocollagen, or synthetic polymers, such as poly(L-lysine), polyethyleneimine (PEI) or dendrimers, which form complexes with the nucleic acids of the invention; liposomes; cationic liposomes; galactosylated liposomes; liposomes coated with a ligand allowing them to target a cell type such as immunoliposomes coated with an antibody specific for the target cell (Zheng et al., 2009); liposomes positioned within a nanoparticle formed by polymers (Carmona et al., 2009) or even multilayer films of polycations and polyanions.
Excipients such as lactose, sodium citrate, calcium carbonate, dicalcium phosphate and disintegrating agents such as starch, alginic acids and certain complex silicates combined with lubricants such as magnesium stearate, sodium lauryl sulfate and talc can be used to prepare tablets. To prepare a lozenge, it is advantageous to use lactose and high molecular weight polyethylene glycols. Aqueous suspensions contain emulsifiers or agents that facilitate suspension. Diluents such as sucrose, ethanol, polyethylene glycol, propylene glycol, glycerol and chloroform or mixtures of these are also usable.
Adjuvants such as aluminum salts (for example aluminum hydroxide, aluminum phosphate, aluminum sulfate), surfactants (such as lysolecithin, pluronic polyols, polyanions, peptides and emulsions), complete and incomplete Freund's adjuvant, MPL-TDM adjuvant (monophosphoryl lipid A, synthetic trehalose dicorynomycolate), tyrosine, aluminum, saponins such as Stimulon™, and cytokines can also be added to improve the efficiency of the composition.
The RNA sequences of the invention can be prepared with an agent, such as injectable microspheres, bioerodible particles, polymeric compounds (such as polylactic acid or polyglycolic acid), beads or liposomes that may provide controlled or sustained release of the product.
Examples of dietarily-acceptable supports comprise, for example, sugars, saponins, etc. The composition may also include one or more other active ingredients chosen preferably among an agent usable in the treatment of a laminopathy, in particular in treating Hutchinson-Gilford syndrome or HGPS (also known as progeria and which consists in an early and accelerated aging in humans), obesity, diabetes, cancer, degenerative diseases, in particular neurodegenerative (e.g. leukodystrophy or hereditary spastic paraplegia still identified as SPG35), a stress or infertility.
An active principle in the treatment of obesity may be, for example, leptin or one of its derivatives.
An active principle in the treatment of diabetes may be, for example, insulin or one of its derivatives.
An active principle in the treatment of cancer may be, for example, a conventional cytotoxic chemotherapeutic agent selected from an inhibitor of DNA replication (such as DNA binding agents, in particular intercalating or alkylating compounds), an anti-metabolite agent (such as DNA polymerase inhibitors or a topoisomerase I or II inhibitor), an anti-mitogenic agent (e.g., an alkaloid), and an agent blocking the growth of a cancerous tumor (such as a tyrosinase inhibitor or a monoclonal antibody).
The RNA according to the invention (possibly comprised or expressed using another product according to the invention described in this text) and the other active compound or compounds, can be administered simultaneously, if applicable in a same composition, or sequentially.
The products of the invention (nucleic acid sequences, vectors, cells, compositions) can be adapted for intravenous, oral, sublingual, parenteral, rectal, topical, transdermal, subcutaneous, mucosal, intramuscular, intrapulmonary, intranasal, vaginal, etc., administration according to standard protocols well known to the person skilled in the art.
Preferably, the product is adapted for oral administration and presented in a solid or liquid form. The product can be in the form of a food, tablet, capsule, pill, dragee, lozenge, granules, or oral solution. In the case of parenteral administration, it is preferably in the form of a liquid solution, an emulsion or a suspension. In the case of intravenous, intradermal or subcutaneous administration, it is typically in the form of a solution for injection.
The nucleotide sequence of interest can also be administered by electroporation, into the muscles or through the skin of the subject.
The dosage (or therapeutically-effective quantity) is easily determined by the skilled person so that the desired effects (i.e., extending the lifespan, fighting the harmful effects of aging, stress and/or infertility) are attained. The specific dose of the product should be adjusted to the subject concerned and the desired application. It depends on several factors, including the weight, health status, sex and diet of the subject, the administration route, absorption and excretion rates, and possible combination with one or more other active molecules.
The total daily dose of the product administered to a human subject in a single dose or in several doses may be, for example, comprised between 1 μg and 20 mg per kilo, preferably between 100 μg and 5 mg. The administrations can be weekly or daily or even repeated several times a day. The RNAs or compositions according to the invention comprising them can be administrated in the form of a unit dose comprising 0.05 to 20 mg of RNA, preferentially 0.1 to 5 mg.
In one particular embodiment, a RNA sequence of interest of the invention is used in a therapeutic composition, for example a vaccine.
In another particular embodiment, a RNA sequence of interest of the invention is used in a cosmetic composition.
The present invention concerns in particular a product such as described in this text consisting in, or comprising, a RNA sequence or a DNA sequence of interest according to the invention for use as a medicament.
It also concerns a product or composition according to the invention for use i) to prevent or treat a pathology, an abnormality, a disorder or an apparent or functional deterioration related to a mechanism of aging, ii) to extend the lifespan of a subject, or iii) to increase the resistance of a subject to a stress.
In one particular aspect, the present invention relates to the use of such a product in a therapeutically-effective quantity for the preparation of a pharmaceutical composition intended i) to prevent or treat a pathology, an abnormality, a disorder or an apparent or functional deterioration related to a mechanism of aging, ii) to extend the lifespan of a subject, or iii) to increase the resistance of a subject to a stress.
In still another particular aspect, the present invention concerns the use of such a product for the preparation of a cosmetic composition.
The term “treatment” as used in this document refers to improvement or resolution of symptoms, slowing the progression of the disease or aging process, stopping the progression of the disease or resolution of the disease.
The inventors have demonstrated the surprising efficacy of the RNA sequences according to the invention in delaying aging process(es) and fighting pathologies and harmful effects associated with these process(es).
The inventors have notably demonstrated that the overexpression in Drosophila of snoRNA:Ψ28S-1153 of sequence SEQ ID NO: 1 spectacularly doubles the lifespan of said Drosophila. In particular, they demonstrated that mutant flies for snoRNA:Ψ28S-1153 have more neurodegenerative lesions than wildtype flies at 40 days old (
The inventors have demonstrated that the overexpression of a RNA sequence of interest according to the invention permits extending the life of a subject, delaying the mechanisms of aging and fighting the harmful effects associated with these mechanisms. In particular, they showed that this overexpression is neuroprotective and serves in particular to prevent or treat a degenerative disease, in particular neurodegenerative, typically neurodegenerative diseases associated with accumulation of iron which result in demyelination in the brain such as, for example, neurodegenerative diseases caused by one or more mutations of the fa2h gene. The invention also particularly permits treating leukodystrophies (typically those related to mutations of the fa2h gene) or hereditary spastic paraplegia (typically SPG35 hereditary spastic paraplegia). It also permits preventing or treating diabetes, a cancer, or a fertility or sterility problem (
“Subject” means any living being that could benefit from such a treatment, regardless of its sex or age. Preferably, the subject is an adult subject. The subject may be an insect such as a Drosophila, or an animal, for example a mammal (preferably a primate or a human being) or a rodent (preferably a mouse or rat).
Preferably, the subject i) does not express the RNA sequence of interest or expresses an abnormal version of said RNA sequence, ii) is a subject experiencing conditions of stress (particularly a subject having reached sexual maturity, preferably an elderly subject) such as fasting, heat shock, oxidative stress (such as paraquat exposure) or a stress (in the intestine) responsible for a detectable cellular proliferation or deregulation of the Delta/Notch pathway, and/or iii) is a subject suffering from a disease related to or promoted by the aging, typically a degenerative disease, in particular neurodegenerative, a laminopathy such as progeria, obesity, diabetes, cancer or fertility problems (particularly including infertility or sterility).
In a particular embodiment, the genome of the subject likely to benefit from the invention i) does not express a RNA of interest sequence as described in this text, ii) expresses an abnormal version of said RNA sequence of interest, or iii) contains a DNA sequence comprising a mutation responsible for the non-expression or abnormal (i.e. non-functional) expression of said RNA sequence of interest.
The normal (wildtype) version of the DNA sequence can be chosen, for example, from among sequences SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28 and SEQ ID NO: 30, identified previously. A mutation likely to affect the normal version of the DNA sequence, i.e., to impede the expression of a RNA sequence of interest according to the invention, is typically chosen from among a deletion, an addition and/or a substitution of one or more nucleotides.
The term “longevity” or “lifespan” refers to the lifespan for which a subject is programmed as a biological species, living under ideal conditions and in the absence of disease or accident. “Maximum longevity” or “maximum lifespan” is the maximum lifespan the individual of a given species can attain. For practical purposes, the maximum longevity of a subject is estimated by the maximum age reached by one of the members of a population. “Mean longevity” or “mean lifespan” is the age at which 50% of a given population survives.
A widely-recognized method to measure the effect of a treatment on “extension of lifespan” is by reference to maximum longevity or mean longevity. If a treatment significantly increases the maximum or mean longevity of a group of subjects relative to a group of control subjects, then there is considered to be an extension of lifespan and delay of aging.
In Drosophila, sexual maturity is reached, on average, at the age of one day. The mean lifespan is around 30 days. The maximum lifespan is comprised between around 60 and 80 days depending on the Drosophila species and line and the living or rearing conditions. In mice, sexual maturity is reached, on average, 42 days after birth. The mean lifespan is around 832 days. In human beings, sexual maturity is reached between 9 and 14 years of age. The mean lifespan is 73 years for men and 79 years for women. The maximum lifespan is currently 122 years, 5 months and 14 days. The term “aging” in the context of this invention, is a process of gradual and spontaneous changes ranging from maturation, through childhood and puberty, up to functional decline of the subject. Aging therefore comprises the positive component of development and maturation and the negative component of decline.
The RNA sequences of interest of the invention increase the maximum or mean longevity (or lifespan) of a subject. Preferably, these sequences extend lifespan and delay aging of a subject or a subpopulation of adult subjects, defined, for example, by sex and/or age (i.e. by a minimum age or a maximum age or by an age window).
Using the present invention, extending the lifespan of Drosophila as well as mammals, including mice and, in particular, human beings, by around 50% or even 100%, while improving conditions of aging is typically considered.
Using the RNA sequences of the present invention, it is also possible to fight “the harmful effects of aging”. In the context of the present invention, this expression means the negative component of aging, i.e., decline of the subject. Progressive decline, with age, of physiological capacities varies from one organ to another and from one subject to another. The physiological decline of a subject leads to a reduced ability to respond to an environmental stimulus and increase in the susceptibility and vulnerability to diseases and impairments. The harmful effects of aging encompass the accumulation of undesirable changes that have an impact on weakening a given subject and that can precipitate its death. These changes may be attributed to development, to innate aging processes, to possible genetic abnormalities, to the environment and to diseases that affect or did affect the subject.
Moreover, using the present invention, it is possible to prevent or treat degenerative diseases, in particular neurodegenerative, typically degenerative diseases affecting the central and/or peripheral nervous system.
In a preferred embodiment, the invention permits preventing or treating neurodegenerative diseases associated with the accumulation of iron leading to demyelinization in the brain, in particular neurodegenerative diseases induced by one or more mutations of the fah2 gene. The invention therefore permits treating leukodystrophies (typically those linked to mutations of the fa2h gene) or hereditary spastic paraplegia (typically SPG35 hereditary spastic paraplegia)
In other embodiments, the invention will prevent or treat a pathology selected from among myopathy, Hunter syndrome, dyskeratosis congenita, Prader-Willi Syndrome, Alzheimer's disease, Parkinson's disease, Huntington's disease, multiple sclerosis and amyotrophic lateral sclerosis (ALS).
In another embodiment, the present invention will prevent or treat laminopathies such as Hutchinson-Gilford syndrome (or progeria), mandibuloacral dysplasia (MAD), Emery-Dreifuss muscular dystrophy, atypical Werner syndrome, restrictive dermatopathy, lethal fetal akinesia, and LIRLLC (Generalized lipoatrophy, insulin-resistant diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy), preferably Hutchinson-Gilford syndrome.
In yet another embodiment, the present invention will prevent or treat diabetes or obesity.
It may also participate in the prevention or treatment of cancer or neoplastic process. The cancer is typically a cancer selected from among carcinoma, sarcoma, lymphoma, melanoma, pediatric tumor or leukemia. It may, for example, be breast cancer, ovarian cancer, endometrial cancer, prostate cancer, esophageal cancer, colon cancer, rectal cancer, kidney cancer, lung cancer, thyroid cancer, osteosarcoma, melanoma, leukemia, neuroblastoma, etc.
In one particular embodiment, this invention is particularly useful to fight cancer induced by free radicals such as colon cancer and stomach cancer.
It is also possible to fight problems of infertility or sterility using the product according to the invention. “Infertility” or “sterility” means difficulty conceiving or inability to conceive. In the context of this use, the subject is typically female, sexually mature and having difficulty, for example premature, reproducing. Typically the subject is sterile, infertile or has had an early or premature reduction in fertility. The RNA sequences of interest according to the invention allow treating infertility or restoring, increasing, enhancing or stimulating the fertility of the treated subject.
The present invention also concerns a method for treating a pathology, abnormality, disorder, harmful effect or apparent or functional deterioration related to a mechanism of aging or to a stress, such as described in this text.
The invention also provides a method for evaluating the cosmetic or therapeutic efficacy of a test compound to fight the harmful effects of aging or a stress as well as against the pathologies associated with such a stress or such a mechanism of aging or for fighting infertility.
“Test compound” means any compound potentially involved in the fight against the harmful effects of aging, against a stress or against infertility. For example, it can be a natural or chemical molecule, a metal, an irradiating agent, etc.
A compound can be tested for its potential therapeutic efficacy, i.e., its ability to prevent, treat or enhance the treatment of diseases and harmful effects of aging or a stress, e.g. laminopathy, a degenerative disease or a cancer as described previously, to prevent, treat or enhance the treatment of diabetes or obesity, or to prevent, treat or enhance the treatment of infertility.
A compound can also be tested for its potential cosmetic efficacy, i.e., its ability to improve the physical appearance of the subject and better fight an apparent deterioration of the subject related to a mechanism of aging. The test compound can prove effective, for example, in the cosmetic treatment of the epidermis, body hair and/or capillary system, nails, lips, external genital organs, teeth or mucosa.
In a first embodiment, the method described in the invention comprises the following steps:
i) exposure of a cell, a population of cells or a tissue, not expressing the RNA sequence according to the invention or expressing an abnormal version of said RNA sequence; or a transgenic mouse according to the invention,
ii) evaluation of the effects, if any, of the test compound on the phenotype of said cell(s) or said tissue or said transgenic mouse, and
iii) determination of the cosmetic or therapeutic efficacy of said test compound, a restoration of the activity and/or expression of said RNA sequence being correlated with an efficacy of said test compound.
The cosmetic or therapeutic efficacy of said test compound can be evaluated or determined in reference to a control value. This control value can be established from the level of activity and/or expression of said RNA sequence in a cell, a population of cells or a tissue not expressing, or expressing an abnormal version of said RNA sequence or in a transgenic mouse according to the invention.
If the activity and/or expression of said RNA sequence present in the cell, population of cells, tissue or transgenic mouse exposed to the test compound is greater than the activity and/or expression of the RNA sequence in the cell, population of cells or tissue not expressing, or expressing an abnormal version of said RNA sequence or in said transgenic mouse of the invention, then the test compound has cosmetic or therapeutic efficacy.
In a second embodiment, the method described in the invention comprises the following steps:
i) exposure of a cell according to the invention comprising a RNA sequence according to the invention, a population of cells or a tissue comprising a cell according to the invention,
ii) evaluation of the effects, if any, of the test compound on the phenotype of said cell or population of cells or said tissue, and
iii) determination of the cosmetic or therapeutic efficacy of said test compound, an increase of the activity and/or expression of said RNA sequence being correlated with an efficacy of said test compound.
According to this aspect of the invention, a control value can be established from the level of activity and/or expression of said RNA sequence in a cell or a population of cells expressing said RNA sequence.
In this case, if the activity and/or expression of said RNA sequence present in the cell or population of cells exposed to the test compound are greater than the activity and/or expression of the RNA sequence in the cell or population of cells expressing said RNA sequence, then the test compound has cosmetic or therapeutic efficacy.
The level of activity and/or expression of the RNA sequence can be quantified using techniques known to the skilled person, typically by quantitative PCR or immunohistochemistry (staining by antibodies directed against the genes/proteins regulated by the snoRNA of interest).
The therapeutic effect can also be evaluated, for example, by determining the lifespan of the cells, by measuring the number of cell divisions, etc.
Preferably, the cell or population of cells exposed to the test compound is of intestinal or ovarian origin. Preferred cells can be chosen from among the cells mentioned in this text, typically from among enteroblasts, enterocytes, entero-endocrine cells, intestinal stem cells, nurse cells, typically nurse cells of the ovarian chamber, oocytes, ooblasts, etc.
Other aspects and advantages of the present invention will appear upon reading the figures and examples that follow, which should be considered as illustrative and non-limiting.
A) Heat Shock: The F4 mutants are more resistant than the controls (females only). Flies overexpressing the snoRNA (G5), as well as F4 mutants provided with the transgene (F4; G5) are more resistant than the controls (males and females).
B) Fasting: The F4 mutants are more resistant than the controls (males and females). Flies over-expressing the snoRNA (G5) are more resistant (females only). F4 mutant female flies provided with the transgene (F4; G5) are similar to the control flies; therefore the wildtype is restored by the transgene.
C) Paraquat: The F4 mutants are more resistant than the controls (males and females). Flies over-expressing the snoRNA (G5) are more resistant (females only). F4 mutant flies provided with the transgene (F4; G5) are similar to the control flies, therefore the wildtype is restored by the transgene.
A) in the wildtype control mice (Canton-S), the snoRNA is expressed in the epithelial cells of the intestine. Blue: DNA staining in the nucleus by DAPI. Red: snoRNA staining. Note that the snoRNA staining (red points) is distinct and complementary to that of the nucleus (blue), demonstrating that this latter is localized in the nucleolus.
B) In the F4 mutant (deletion of the snoRNA), the blue staining is seen (DAPI) but no red staining, because the snoRNA is deleted and therefore not expressed.
C) control flies, wildtype (Canton-S). The snoRNA is expressed in ovarian nurse cells.
D) F4 mutant flies. The snoRNA is not expressed in the ovaries.
A) Targeted expression under the control of esg-Ga14 (esg-Ga14, F4/F4; UAS-8M/+)
B) Targeted expression under the control of Su(H)-Ga14 (Su(H)-GBE-Ga14, F4/F4; UAS-8M/+).
C) Targeted expression under the control of Delta-Ga14 (Delta-Ga14, F4/F4; UAS-8M/+).
A) Fasting: Targeted expression of the snoRNA (UAS-8M) under the control of Myo1A-Ga14. There is a clear increase in resistance in flies expressing the snoRNA (Myo, F4/F4; 8M/+) relative to the two control lines.
B) Fasting: Targeted expression of the snoRNA (UAS-8M) under the control of esg-Ga14. There is a clear increase in resistance in flies expressing the snoRNA (esg, F4/F4; 8M) relative to the two control lines.
C) Fasting: Targeted expression of the snoRNA (UAS-8M) under the control of Su(H)-Ga14. There is a clear increase in resistance in flies expressing the snoRNA (Su(H), F4/F4; 8M) relative to the two control lines.
D) Heat shock at 36° C.: Targeted expression of the snoRNA (UAS-8M) under the control of Su(H)-Ga14. There is a clear increase in resistance in flies expressing the snoRNA (Su(H), F4/F4; 8M) relative to the two control lines.
A) Model of intestinal epithelium regeneration in the adult Drosophila.
B) Model of the Notch function in entero-endocrine cells in the Drosophila (embryo, larva, pupa, adult) and in mammals. Dl=Delta, N=Notch, NO=no Notch signal. This diagram clearly shows the perfect similarity between the intestinal epithelium of Drosophila and that of humans.
This experiment is part of the search for the neural basis involved in locomotor behavior in Drosophila and the study of the relationship between structure and function of the central complex and especially the ellipsoid body. In this context, screening a library of P[GAL4] enhancer trap lines permitted identifying the P[GAL4]4C line that is specifically expressed in the ellipsoid body (
snoRNA:Ψ28S-1153 was identified at this locus in position 67331 (
At the same time as the study done to quantify the locomotor activity of the flies via the targeted expression of tetanus toxin in labelled ring neurons of the P[GAL4] 4C line, the inventor observed that these flies had a very short lifespan and decided to precisely quantify said life span of the P[GAL4]4C/UAS-tetanus-toxin flies, as well as that of the F4 flies (mutated at locus 4C). Thus the F4 flies have a short lifespan (of around 30% relative to wildtype control flies), suggesting that the snoRNA deletion could affect lifespan (longevity) (
3) Genesis of a Transgenic Line Containing the Genomic Region of the snoRNA (Youth) for Purposes of Restoring the Wildtype Phenotype (“Rescue”).
In order to demonstrate that the phenotype of the F4 mutant is actually due to the deletion of the snoRNA, a line of transgenic Drosophila bearing a genomic DNA sequence of 1723 by of the region (from 66377 to 68100), comprising the snoRNA (
Next, in order to verify that the transgene is functional and can rescue the F4 mutation (i.e., restore the wildtype phenotype, that is restore a lifespan equivalent to that observed with no F4 deletion), the inventor introduced these transgenic lines in the context of the F4 genetic mutant, by standard genetic crosses (F4; G4 and F4; G5) It could thus be demonstrated that the transgene could rescue the phenotype due to the mutation responsible for the reduction in lifespan (
It is now generally acknowledged that genes acting on longevity generally increase stress resistance. The inventor has verified and obtained confirmation that overexpression of this snoRNA is effectively able to increase the lifespan of the subject concerned under stress conditions, such as fasting, heat shock and oxidative stress (induced by paraquat) (
Males and females are raised together in standard tubes containing feed for 3 days. At age 3 days, the males and females are distributed separately by group of 20 in a standard tube containing feed. To subject the flies to heat shock, tubes containing the flies are placed in an incubator at 36° C. The number of dead flies is counted every 6 hours. For heat shock (36° C.), in
Like the heat resistance test, males and females are raised together in standard tubes containing feed for 3 days. At age 3 days, the males and females are distributed separately by group of 20 into a tube containing a filter paper and 400 μL of water in order to prevent desiccation. The flies are kept in a humid room at 24° C., and the number of dead flies is counted every 6 hours. For fasting, in
Paraquat (1,1′-dimethyl-4,4′-bipyridinium dichloride) reduces NADH, which generates stable paraquat radicals, which react with oxygen to generate ROS (reactive oxygen species). Consequently, the ROS cause cell damage (Rzezniczak et al., 2011). Like for the previous tests, males and females are raised together in standard tubes containing feed for 3 days. At age 3 days, the males and females are distributed separately by group of 20 into an empty standard tube in order to fast them for 6 hours. Next, the flies are transferred into a tube containing a filter paper and 450 μl of 20 mM paraquat diluted in 1% sucrose to promote dietary intake. The flies are kept in a humid room at 24° C., and the number of dead flies is counted every 6 hours.
For oxidative stress, in
In summary, the F4 mutant flies are more resistant than the control flies, while overexpression (G5) further increases this resistance (an effect that is more marked and consistent in females than in males). Moreover, in both tests (fasting and oxidative stress) the expression of the transgene in the F4 mutant (F4; G5) restores fly survival, especially in females. Thus, contrary to longevity where the F4 mutation reduces lifespan, the F4 mutation increases resistance in the three stress tests done in young three-day-old flies, and this effect can be restored by the genomic transgene of the snoRNA (in two tests). In conclusion, modulation of expression (suppression, reduction or increase) of the “youth” snoRNA changes the lifespan of the subjects tested.
In order to determine in what cells and/or tissues the snoRNA of interest is expressed and acts, the space-time expression profile of this snoRNA was determined in the context of the invention, in the adult fly, by in situ hybridization (HIS), using an anti-sense snoRNA. Tyramide was used to amplify labelling. In both males and females, the youth snoRNA is expressed in the intestine wall (epithelium) (
Targeted expression (ectopic) of snoRNA (UAS-8M) in types of cells other than intestine epithelium via the use of three other distinct Ga14 driver lines was done: esg-Ga14 (esg-Ga14, F4/F4; UAS-8M/+) and Delta-Ga14 (Delta-Ga14, F4/F4; UAS-8M/+) targeting intestinal stem cells (ISCs), while Su(H)-Ga14 (Su(H)-GBE-Ga14, F4/F4; UAS-8M/+) target enteroblasts (
The inventor has demonstrated, by two independent approaches, that a targeted expression in intestine cells is sufficient to restore the stress resistance phenotype. It could be demonstrated, by the in situ hybridization technique, done from genomic transgenic lines (those increasing longevity: G5, as well with another independent insertion (G4) that the snoRNA is expressed in intestinal cells and that, for regulation of longevity, the expression of the snoRNA in intestinal cells is sufficient.
In order to confirm this first result, the snoRNA was targeted only in intestinal cells, by using the P[Ga14] binary expression system. A plasmid vector (p[UAS-snoRNA]) was constructed in which the snoRNA of interest (only 148 bp) is placed under the control of regulator elements (Upstream Activating Sequence: UAS) of Ga14. Transgenic fly lines (UAS-snoRNA: 4M, 5M and 8M) were then generated. For targeted expression, so-called “driver” lines of transgenic flies containing a transgene (pChs-Ga14) (plasmid vector lines Myo1A-Ga14, esg-Ga14 (escargot-Ga14), Su(H)GBE-Ga14, and Dl-Ga14 (Delta-Ga14)), known to be expressed in particular in intestinal cells were used (Jiang and Edgar, 2011; Takashima et al., 2011). Next, these various transgenes were placed in the F4 mutant genetic background, and it was demonstrated, by in situ hybridization, that the snoRNA is actually expressed in these various types of intestinal cells (
These experiments clearly show that manipulating these snoRNAs in intestinal cells, and more particularly in enterocytes, is necessary and sufficient to restore stress resistance. These experiments, although conducted in Drosophila, permit suggesting that re-expression (restoration of expression or rescue) or overexpression of the snoRNA in epithelial cells of the intestine is able to lead to an increase in lifespan in mammals and in particular in humans.
Sequence homology searching showed that these snoRNA also exist in the 11 other species of Drosophila whose genome is available (
Moreover, a homology search and especially via the RNA structure (using INFERNAL software) allowed identifying a homolog in humans, located on chromosome 11, at position: 12822722-12822811 (
Like in Drosophila, it is very probable that the overexpression of this gene and/or a synthetic analog (either genetically or by oral administration, or by injection) will extend the human lifespan. Such expression is also able to protect against the harmful effects of various degenerative diseases.
Since F4 flies have a very short lifespan, while flies overexpressing the snoRNA (G5) live longer, the old flies (40 days old) were studied in order to check for the presence of any neurodegenerative lesions (more or fewer holes of larger or smaller size present in the brain). Overall, in the control flies (Canton-S), around 60% of flies present lesions (but note that 50% of the CS flies are already dead at 40 days) (
Similarly, in order to ascertain whether the neuroprotection provided by the snoRNA has effects on physiological parameters such as sensorimotor parameters, the locomotor activity of flies older than 40 days was quantified (by video-tracking) (Martin, 2004) and compared to those of young flies, aged 4 days (
In females, the snoRNA is also expressed in the ovaries and more precisely in nurse cells (
The snoRNA can be administered either orally (per os) or by injection. Other administration routes such as, for example, inhalation and local/cutaneous application can also be used depending on the type of vector used.
As the experiments conducted as part of the invention show, oral administration of the snoRNA is possible given its stability and in vitro resistance as well as its ability to act locally on the cells of the intestinal wall (enteroblasts, enterocytes, ISCs). As explained previously, the administration of the snoRNA of interest is therefore able to permit expression that would otherwise be absent (or, in other words, to rescue an existing mutation) or, if necessary, permit overexpression, in order to protect the intestinal wall from damage while maintaining a better hormonal and metabolic equilibrium.
In both mammals and Drosophila, it was shown that the delta/notch genes regulate the differentiation of intestine (gut) progenitor cells, while the Wnt signalling pathway participates in maintenance and proliferation of ISCs. Likewise, the cytokine signalling pathways (Upd/Jak/Stat) and the EGFR (Epidermal Growth Factor Receptor) pathway regulate the proliferation of ISCs (
Our experiments show that the snoRNA of interest according to the invention is able to regulate certain genes, such as notch, delta, JNK, EGFR, etc. (
We have demonstrated that the youth snoRNA regulates splicing (quantity of spliced RNA) of the klarsicht gene (
We have demonstrated that the youth snoRNA regulates splicing (quantity of RNA spliced) of gene CG30502 coding for fatty acid 2-hydroxylase (fa2h) (
As mentioned previously, snoRNA mutants (F4) present fat body hypertrophy, visible both at the abdomen and around the brain in the head capsule (
By a RT-PCR approach, we have demonstrated the existence of homologous sequences, more precisely orthologous sequences, to the youth snoRNA (first identified in the Drosophila) concretely expressed in mammals (
| Number | Date | Country | Kind |
|---|---|---|---|
| 1360889 | Nov 2013 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2014/073991 | 11/7/2014 | WO | 00 |
