Patent Application
20100178280
The present invention relates to a pharmaceutical composition comprising (i) a nucleic acid molecule encoding a protein having Sirt7 function wherein said nucleic acid molecule (a) has the sequence of SEQ ID NO: 1, 3, 5 or 7; (b) encodes a protein having the sequence of SEQ ID NO: 2, 4, 6 or 8; (c) hybridizes under stringent conditions to the molecule of (a) or (b); or (d) has an identity on the nucleic acid level of at least 80% with the molecule of (a), (b) or (c); (ii) a vector comprising the nucleic acid molecule of (i); (iii) a host cell comprising the vector of (ii); or (iv) a protein encoded by the nucleic acid molecule of (i). The pharmaceutical composition may be used, for example, in the treatment of age-related diseases. Furthermore, the invention relates to screening methods for the identification of compounds useful in the treatment of age-related diseases.
Throughout this specification, several documents are cited. The disclosure content of these documents is herewith incorporated by reference (including all product descriptions and manufacturers instructions).
As the progress in modern medicine has lead to a tremendous increase in lifespan in the industrialized countries, the need for the treatment or amelioration of age-related diseases has concurrently increased since a growing part of the population suffers from such diseases. Several genes that are involved in aging and lifespan control have been proposed. These so-called longevity genes are often involved in pathways that guarantee better survival under conditions such as food deprivation, cold or other types of environmental stress (Porcu and Chiarugi, Trends in Pharmacological Sciences 2005, 26: 94).
One example of such longevity genes are the silent information regulator (SIR) genes of the budding yeast S. cerevisiae. These are nonessential genes required for transcriptional repression of several genomic loci. Among these genes, Sir2 is unique since it belongs to a large family of closely related proteins present in eukaryotic as well as in prokaryotic species. Sir2 is responsible for promoting longevity in yeast mother cells by inhibiting recombination in the rDNA (ribosomal DNA) repeats since the recombinational excision and subsequent accumulation of extrachromosomal rDNA circles is involved in senescence. In addition, Sir2 family members have been suggested to mediate the lifespan extending effects of caloric restriction, a mechanism which is capable of extending the lifespan of a diverse range of organisms ranging from yeast to mammals (Mostoslaysky et al., Cell 2006, 124: 315).
The fact that several mechanisms that regulate lifespan are well conserved across species (e.g. caloric restriction) led to the speculation that mammalian Sir2 family members are also involved in lifespan regulation in mammals (North and Verdin, Genome Biology 2004, 5: 224).
There are seven mammalian Sir2 family members which are named Sirt1 to Sirt7 wherein Sirt1 exhibits the closest relationship to Sir2. In contrast to Sir2 which exclusively deacetylates histones, Sirt1 has a diverse list of substrates. Although the lifetime prolonging effects of Sirt1 have not unambiguously been shown in mammals, its role in the improvement of stress resistance and in the modulation of the metabolism in other model organisms led to the assumption that it plays an important role in the regulation of lifespan even in mammals. Two of the Sirt1 target genes, namely p53 and PGC-1α mediate longevity associated effects: p53 is deacetylated by Sirt1 leading to a decreased rate of stress-induced apoptosis and PGC-1α forms a complex with Sirt1 thereby promoting gluconeogenesis in liver and free fatty acid mobilization upon fasting. This effect leads to the inhibition of insulin/IGF signalling and seems to be conserved between yeast and mammals. Inhibition of this signalling pathway appears to be also responsible for the lifespan extending effects of caloric restriction (Mostoslaysky et al., Cell 2006, 124: 315).
Only little is known about the longevity related functions of other mammalian Sirts although recent data indicate the involvement of Sirt6 in genomic stabilization (Mostoslaysky et al., Cell 2006, 124: 315). Almost nothing is known with respect to Sirt7. As pointed out in Porcu and Chiarugi (2005), Sirt7 does not show any deacetylase activity. Hence, the prior art clearly teaches away from the involvement of Sirt7 in processes that regulate ageing based on a reduced p53 activity. Furthermore, it has also been postulated that Sirt7 cannot exhibit a deacetylase activity because it contains a serine residue at position 115 instead of a glycine in the enzymatic core domain whereas the prior art describes that the glycine residue is essential for the deacetylating activity (Imai et al., Nature 2002, 403: 795; Michita et al., Mol. Biol. Cell 2005, 16: 4623; North et al., Mol. Cell 2003, 11: 437).
Accordingly, the prior art clearly teaches away from the use of Sirt7 as a target for pharmaceutical interventions for treating age-related diseases. In view of the ageing community the technical problem underlying the present invention was the provision of means and methods for treating age-related diseases.
The solution to this problem is achieved by providing the embodiments as characterized in the claims.
Accordingly, the present invention relates to a pharmaceutical composition comprising (i) a nucleic acid molecule encoding a protein having Sirt7 function wherein said nucleic acid molecule (a) has the sequence of SEQ ID NO: 1, 3, 5 or 7; (b) encodes a protein having the sequence of SEQ ID NO: 2, 4, 6 or 8; (c) hybridizes under stringent conditions to the molecule of (a) or (b); or (d) has an identity on the nucleic acid level of at least 80% with the molecule of (a), (b) or (c); (ii) a vector comprising the nucleic acid molecule of (i); (iii) a host cell comprising the vector of (ii); or (iv) a protein encoded by the nucleic acid molecule of (i).
In accordance with the present invention, the term “pharmaceutical composition” relates to a composition for administration to a patient, preferably a human patient. The pharmaceutical composition of the invention comprises the compounds recited above. It may, optionally, comprise further molecules capable of altering the characteristics of the compounds of the invention thereby, for example, stabilizing, modulating and/or activating their function. The composition may be in solid, liquid or gaseous form and may be, inter alia, in the form of (a) powder(s), (a) tablet(s), (a) solution(s) or (an) aerosol(s). The pharmaceutical composition of the present invention may, optionally and additionally, comprise a pharmaceutically acceptable carrier. Examples of suitable pharmaceutical carriers are well known in the art and include phosphate buffered saline solutions, water, emulsions, such as oil/water emulsions, various types of wetting agents, sterile solutions, organic solvents including DMSO etc. Compositions comprising such carriers can be formulated by well known conventional methods. These pharmaceutical compositions can be administered to the subject at a suitable dose. The dosage regimen will be determined by the attending physician and clinical factors. As is well known in the medical arts, dosages for any one patient depend upon many factors, including the patient's size, body surface area, age, the particular compound to be administered, sex, time and route of administration, general health, and other drugs being administered concurrently. The therapeutically effective amount for a given situation will readily be determined by routine experimentation and is within the skills and judgement of the ordinary clinician or physician. Generally, the regimen as a regular administration of the pharmaceutical composition should be in the range of 1 μg to 5 g per day. However, a more preferred dosage might be in the range of 0.01 mg to 100 mg, even more preferably 0.01 mg to 50 mg and most preferably 0.01 mg to 10 mg per day.
“Nucleic acid molecules”, in accordance with the present invention, include DNA, such as cDNA or genomic DNA, and RNA. Further included are nucleic acid mimicking molecules known in the art such as synthetic or semi-synthetic derivatives of DNA or RNA and mixed polymers, both sense and anti-sense strands. Such nucleic acid mimicking molecules or nucleic acid derivatives according to the invention include phosphorothioate nucleic acid, phosphoramidate nucleic acid, 2′-O-methoxyethyl ribonucleic acid, morpholino nucleic acid, hexitol nucleic acid (HNA) and locked nucleic acid (LNA) (see Braasch and Corey, Chem Biol 2001, 8: 1). LNA is an RNA derivative in which the ribose ring is constrained by a methylene linkage between the 2′-oxygen and the 4′-carbon. They may contain additional non-natural or derivative nucleotide bases, as will be readily appreciated by those skilled in the art.
In a preferred embodiment the nucleic acid molecule(s) is/are DNA.
“A protein having Sirt7 function” in accordance with the present invention is a protein exhibiting for example deacetylation of p53. Furthermore, said protein may also be capable of deacetylating FOXO, NFκB or p300, downregulating PEPCK, activating FAS and de-phosphorylating p38.
As regards the nucleic acid molecule referred to in (i) above, the sequence of SEQ ID NO: 1 and 3 relates to the Sirt7 nucleic acid sequence of mouse, the sequence of SEQ ID NO: 5 relates to the Sirt7 nucleic acid sequence of rat and the sequence of SEQ ID NO: 7 relates to the Sirt7 nucleic acid sequence of human.
The nucleic acid molecule referred to in (i) above encodes for example a protein having the sequence of SEQ ID NO: 2 and 4 which relates to the Sirt7 amino acid sequence of mouse, or having the sequence of SEQ ID NO: 6 which relates to the Sirt7 amino acid sequence of rat or having the sequence of SEQ ID NO: 8 which relates to the Sirt7 amino acid sequence of human.
The term “protein” as used herein is well known to the skilled person. The term “protein” may be further specified as referring to any high molecular mass compound generally consisting of one or more linear chains of the 20 amino acids of the genetic code joined by peptide bonds, occurring in living systems. The amino acids in the chains may be naturally modified by e,g, glycosylation, acetylation, phosphorylation and similar modifications which are well known in the art. The term “protein” refers to single-domain proteins as well as to multi-domain proteins and to single chain as well as multiple chain proteins. Furthermore, peptidomimetics of such proteins where amino acid(s) and/or peptide bond(s) have been replaced by functional analogs may also be encompassed by the term “protein”. Such functional analogues include all known amino acids other than the 20 gene-encoded amino acids, such as selenocysteine.
The nucleic acid molecule used in the pharmaceutical composition may be at least 80% identical, preferably at least 90% and more preferably at least 95% identical to the nucleic acid molecule of (i)(a) through (i)(c). It is of note that in mice (North and Verdin, Genome Biology 2004, 5: 224) and rats the amino acids N at position 169 and H at position 188 in SEQ ID NO: 2 are required for the deacetylating activity of the protein while in humans the amino acids N168 and H187 are required. Thus, the nucleotide positions corresponding to these amino acids should preferably be retained when using the aforementioned nucleic acid molecules with the named identity values. Such molecules may be homologous molecules from other species, such as homologs or mutated sequences to mention the most prominent examples. To evaluate the identity level between two nucleotide or protein sequences, they can be aligned electronically using suitable computer programs known in the art. Such programs comprise BLAST (Altschul et al., J. Mol. Biol. 1990, 215: 403), variants thereof such as WU-BLAST (Altschul & Gish, Methods Enzymol. 1996, 266: 460), FASTA (Pearson & Lipman, Proc. Natl. Acad. Sci. USA 1988, 85: 2444) or implementations of the Smith-Waterman algorithm (SSEARCH, Smith & Waterman, J. Mol. Biol. 1981, 147: 195). These programs, in addition to providing a pairwise sequence alignment, also report the sequence identity level (usually in percent identity) and the probability for the occurrence of the alignment by chance (P-value). Programs such as CLUSTALW (Higgins et al., Nucleic Acids Res. 1994, 22: 4673) can be used to align more than two sequences.
The term “hybridizes/hybridizing” as used herein refers to a pairing of a polynucleotide to a (partially) complementary strand of this polynucleotide which thereby form a hybrid.
It is well known in the art how to perform hybridization experiments with nucleic acid molecules. Correspondingly, the person skilled in the art knows what hybridization conditions she/he has to use to allow for a successful hybridization in accordance with item (i)(c), above. The establishment of suitable hybridization conditions is referred to in standard text books such as Sambrook, Russell “Molecular Cloning, A Laboratory Manual”, Cold Spring Harbor Laboratory, N.Y. (2001); Ausubel, “Current Protocols in Molecular Biology”, Green Publishing Associates and Wiley Interscience, N.Y. (1989), or Higgins and Hames (Eds.) “Nucleic acid hybridization, a practical approach” IRL Press Oxford, Washington D.C., (1985).
“Stringent conditions” refers to hybridization conditions which comprise, e.g. an overnight incubation at 65° C. in 4×SSC (600 mM NaCl, 60 mM sodium citrate) followed by washing at 65° C. in 0.1×SSC for one hour. Alternatively, hybridization conditions can comprise: an overnight incubation at 42° C. in a solution comprising 50% formamide, 5×SSC (750 mM NaCl, 75 mM sodium citrate), 50 mM sodium phosphate (pH 7.6), 5×Denhardt's solution, 10% dextran sulphate, and 20 μg/ml denatured, sheared salmon sperm DNA, followed by washing in e.g. 0.1-0.5×SSC at about 55-65° C. for about 5 to 20 min. Said conditions for hybridization are also known by a person skilled in the art as “highly stringent conditions for hybridization”. Also contemplated are nucleic acid molecules that hybridize to the polynucleotides of the invention at lower stringency hybridization conditions (“low stringency conditions for hybridization”). Changes in the stringency of hybridization are primarily accomplished through the manipulation of formamide concentration (lower percentages of formamide result in lowered stringency), salt conditions, or temperature. For example, lower stringency conditions include an overnight incubation at 50° C. in 4×SSC or an overnight incubation at 37° C. in a solution comprising 6×SSPE (20×SSPE=3M NaCl; 0.2M NaH2PO4; 0.02M EDTA, pH 7.4), 0.5% SDS, 30% formamide, 100 mg/ml salmon sperm blocking DNA; followed by washes at 50° C. with 1×SSPE, 0.1% SDS. In addition, to achieve an even lower stringency, washes performed following stringent hybridization can be done at higher salt concentrations (e.g. 5×SSC). It is of note that variations in the above conditions may be accomplished through the inclusion and/or substitution of alternate blocking reagents. Typical blocking reagents include Denhardt's reagent, BLOTTO, heparin, denatured salmon sperm DNA, and commercially available proprietary formulations. The inclusion of specific blocking reagents may require modification of the hybridization conditions described above, due to problems with compatibility. Such modifications can generally be effected by the skilled person without further ado. The embodiment recited herein above preferably refers to highly stringent conditions and alternatively to conditions of lower stringency.
The biochemical functions of the mammalian sirtuins have predominantly been studied for Sirt1 which is the closest homologue of the yeast Sir2 which is known to increase the lifespan of yeast by about 30% (Kaeberlein et al., Genes & Dev. 1999, 13: 2570) and of C. elegans by about 50% (Tissenbaum & Guarente, Nature 2001, 410: 227) when present in more than one copy. Several potential target proteins for a Sirt1-dependent deacetylation have been postulated among which are p53, FOXO, NFkB and p300. However, no biologically relevant deacetylation could be demonstrated in vivo. In addition, no unambiguous age-preventive function of Sirt1 has been documented in vivo either. Knock-out of the Sirt1 gene leads to early postnatal lethality. The only sirtuin which appears to be also involved in age-related processes may be Sirt6. However, Sirt6-deficient mice die during the first postnatal month. It turned out that the mechanism underlying the Sirt6 function is the maintenance of genomic stability (Mostoslaysky et al., Cell 2006, 124: 315). In the context of the present invention, it has been surprisingly discovered that Sirt7 is the first mammalian sirtuin which is involved in ageing processes. It plays a major role in the regulation of such processes by improving the ability to respond to different stressors. Of great importance is the discovery that two pathophysiological aberrations, which occur with progressing age in humans, also occur in Sirt7-deficient mice, namely general chronic inflammation and inflammatory cardiomyopathy (see Examples 1 and 4). It was further found that Sirt7 regulates p53 and various genes that control metabolic pathways (see Examples 2 and 5). Deletion of the Sirt7 gene in a mouse in vivo model led to premature aging, reduced ability to respond to adverse living conditions and cardiac disease (Examples 3 to 5). Resveratrol, a substance present in red wine grapes and believed to be responsible for an increased lifespan in red-wine consumers, has been reported to specifically induce Sirt1 (Baur & Sinclair, Nature 2006, Rev. 5: 493) However, the present invention demonstrates that resveratrol is an even more potent inducer of Sirt7 (see Example 2). In accordance with this finding, it is postulated that it is the effect of resveratrol on Sirt7 and not on Sirt1 which counts for the lifespan extending characteristics of this compound. Furthermore, it has been found in the context of the present invention that Sirt7−/− mice exhibit an increase in the Akt/PKB and ras/raf signalling pathways which is accompanied by heart hypertrophy (see Example 5). It is therefore postulated that Sirt7 may inhibit the insulin/IGF pathway which is believed to be the most important lifespan extending mechanism in lower organisms. Accordingly, Sirt7 was identified as a target to prevent age-related diseases either through stimulation of its expression or its enzymatic activities. Furthermore, Sirt7 may even be directly used in pharmaceutical compositions as recited hereinabove to treat age-related diseases. Sirt7 is a unique target for such interventions since other members of the Sirt gene family are involved in developmental processes like Sirt1 or in the maintenance of genomic stability like Sirt6. Consequently, only the use of Sirt7 is promising with respect to the treatment of age-related diseases since it does not interfere with other fundamental, biological processes.
The present invention also relates to a pharmaceutical composition comprising a vector comprising the nucleic acid molecule referred to above. Preferably, the vector is a plasmid, cosmid, virus, bacteriophage or another vector conventionally used e.g. in genetic engineering. Incorporation of the nucleic acid into a vector offers the possibility of introducing the nucleic acid molecule efficiently into the cells and preferably the DNA of a recipient. The recipient may be a single cell such as a cell from a cell line. Such a measure renders it possible to express, when expression vectors are chosen, the respective nucleic acid molecule in the recipient. Thus, incorporation of the nucleic acid molecule into an expression vector opens up the way to a permanently elevated level of the encoded protein in any cell or a subset of selected cells of the recipient.
In a preferred embodiment, the recipient is a mammal. In a more preferred embodiment, the mammal is a human.
The nucleic acid molecule may be inserted into several commercially available vectors. Non-limiting examples include vectors compatible with an expression in mammalian cells like pREP (Invitrogen), pcDNA3 (Invitrogen), pCEP4 (Invitrogen), pMC1neo (Stratagene), pXT1 (Stratagene), pSG5 (Stratagene), EBO-pSV2neo, pBPV-1, pdBPVMMTneo, pRSVgpt, pRSVneo, pSV2-dhfr, pIZD35, pLXIN, pSIR (Clontech), pIRES-EGFP (Clontech), pEAK-10 (Edge Biosystems) pTriEx-Hygro (Novagen), pCINeo (Promega), Okayama-Berg cDNA expression vector pcDV1 (Pharmacia), pRc/CMV, pcDNA1, pSPORT1 (GIBCO BRL), pGEMHE (Promega), pSVL and pMSG (Pharmacia, Uppsala, Sweden), pRSVcat (ATCC 37152), pSV2dhfr (ATCC 37146) or pBC12MI (ATCC 67109).
The nucleic acid molecule referred to above may also be inserted into vectors such that a translational fusion with another nucleic acid molecule is generated. The vectors may also contain an additional expressible polynucleotide coding for one or more chaperones to facilitate correct protein folding.
For vector modification techniques, see Sambrook and Russel (2001), loc. cit. Generally, vectors can contain one or more origin of replication (ori) and inheritance systems for cloning or expression, one or more markers for selection in the host, e.g., antibiotic resistance, and one or more expression cassettes.
The coding sequences inserted in the vector can e.g. be synthesized by standard methods, or isolated from natural sources. Ligation of the coding sequences to transcriptional regulatory elements and/or to other amino acid encoding sequences can be carried out using established methods. Transcriptional regulatory elements (parts of an expression cassette) ensuring expression in eukaryotic cells are well known to those skilled in the art. These elements comprise regulatory sequences ensuring the initiation of the transcription (e.g. translation initiation codon, promoters, enhancers, and/or insulators), internal ribosomal entry sites (IRES) (Owens Proc. Natl. Acad. Sci. USA 2001, 98: 1471) and optionally poly-A signals ensuring termination of transcription and stabilization of the transcript. Additional regulatory elements may include transcriptional as well as translational enhancers, and/or naturally-associated or heterologous promoter regions. Preferably, the nucleic acid molecule is operatively linked to such expression control sequences allowing expression in eukaryotic cells. The vector may further comprise nucleotide sequences encoding secretion signals as further regulatory elements. Such sequences are well known to the person skilled in the art. Furthermore, depending on the expression system used, leader sequences capable of directing the expressed polypeptide to a cellular compartment may be added to the coding sequence of the polynucleotide of the invention. Such leader sequences are well known in the art.
Possible examples for regulatory elements ensuring the initiation of transcription comprise the cytomegalovirus (CMV) promoter, SV40-promoter, RSV-promoter (Rous sarcome virus), the lacZ promoter, the gai10 promoter, human elongation factor 1a-promoter, CMV enhancer, CaM-kinase promoter, the Autographa californica multiple nuclear polyhedrosis virus (AcMNPV) polyhedral promoter or the SV40-enhancer. Examples for further regulatory elements in prokaryotes and eukaryotic cells comprise transcription termination signals, such as SV40-poly-A site or the tk-poly-A site or the SV40, lacZ and AcMNPV polyhedral polyadenylation signals, downstream of the polynucleotide. Moreover, elements such as origin of replication, drug resistance gene, regulators (as part of an inducible promoter) may also be included. Additional elements might include enhancers, Kozak sequences and intervening sequences flanked by donor and acceptor sites for RNA splicing. Highly efficient transcription can be achieved with the early and late promoters from SV40, the long terminal repeats (LTRs) from retroviruses, e.g., RSV, HTLVI, HIVI, and the early promoter of the cytomegalovirus (CMV). However, cellular elements can also be used (e.g., the human actin promoter).
The co-transfection with a selectable marker such as dhfr, gpt, neomycin, hygromycin allows the identification and isolation of the transfected cells. The transfected nucleic acid can also be amplified to express large amounts of the encoded (poly)peptide. The DHFR (dihydrofolate reductase) marker is useful to develop cell lines that carry several hundred or even several thousand copies of the gene of interest. Another useful selection marker is the enzyme glutamine synthase (GS) (Murphy et al., Biochem J. 1991, 227:277; Bebbington et al., Bio/Technology 1992, 10:169). Using these markers, the mammalian cells are grown in selective medium and the cells with the highest resistance are selected. As indicated above, the expression vectors will preferably include at least one selectable marker. Such markers include dihydrofolate reductase, G418 or neomycin resistance for eukaryotic cell culture.
The nucleic acid molecules as described hereinabove may be designed for direct introduction or for introduction via liposomes, phage vectors or viral vectors (e.g. adenoviral, retroviral) into the cell. Additionally, baculoviral systems or systems based on Vaccinia Virus or Semliki Forest Virus can be used as eukaryotic expression system for the nucleic acid molecules of the invention.
Mammalian host cells that could be used include, human Hela, HEK293, H9 and Jurkat cells, mouse NIH3T3 and C127 cells, Cos 1, Cos 7 and CV1, quail QC1-3 cells, mouse L cells and Chinese hamster ovary (CHO) cells. Also within the scope of the present invention are primary mammalian cells such as mouse embryonic fibroblasts (MEF). Alternatively, the recombinant (poly)peptide can be expressed in stable cell lines that contain the gene construct integrated into a chromosome.
In another embodiment, the present invention relates to the use of (i) a nucleic acid molecule encoding a protein having Sirt7 function, wherein said nucleic acid molecule (a) has the sequence of SEQ ID NO: 1, 3, 5 or 7; (b) encodes a protein having the sequence of SEQ ID NO: 2, 4, 6 or 8; (c) hybridizes under stringent conditions to the molecule of (a) or (b); or (d) has an identity on the nucleic acid level of at least 80% with the molecule of (a), (b) or (c); (ii) a vector comprising the nucleic acid molecule of (i); (iii) a host cell comprising the vector of (ii); or (iv) a protein encoded by the nucleic acid molecule of (i) for the manufacture of a pharmaceutical composition for treating age-related diseases.
As described hereinabove, Sirt7 protein, or its corresponding nucleic acid molecule as described above, is a key regulator of age-related processes. Therefore, its use in the preparation of pharmaceutical compositions for the treatment of age-related diseases offers the possibility to specifically target diseases which accompany ageing processes.
The term “age-related diseases” as used herein refers to diseases which can be characterized by the loss of a cell's, organ's or organism's peak function that continues until its failure and death. In humans most physiological functions such as hearing, eyesight, taste, lung capacity, agility, immune response, adaptation to change etc. reach peak ability between the ages of 11 and 20 years old. After that age there is a slow decline in performance as the degenerative process of aging begins. Age-related diseases are well known in the literature, for example in Cutler & Mattson (Ageing Res. Rev. 2006, 5: 221).
In a preferred embodiment, the age-related disease is selected from the group consisting of fibrosis, inflammatory cardiomyopathy, heart hypertrophy, liver degeneration, skeletal muscle degeneration and chronic general inflammation.
Fibrosis generally relates to the formation of scar tissue in organs such as the liver or the heart. Inflammatory cardiomyopathy relates to an abnormal heart condition in which the heart is dilated (poor pumping power), restrictive (impaired ability of the heart to fill) or hypertrophic (enlarged heart). Heart hypertrophy is a disorder in which the heart muscle is so strong that it does not relax enough to fill the heart with blood and so has reduced pumping ability. Skeletal muscle degeneration generally refers to muscle wasting, sarcopenia as well as depletion of muscular tissues and fat stores. Chronic general inflammation generally relates to an infiltration of organs with inflammatory cells such as macrophages and neutrophile lymphocytes as well as increased levels of CRP and IL6. Emerging pathological evidence indicates that major chronic ageing-related diseases such as atherosclerosis, arthritis, dementia, osteoporosis and cardiovascular diseases are inflammation-related.
In another embodiment, the present invention relates to a method for the identification of a compound useful in the treatment of age-related diseases or as a lead compound for the development of an agent for treating age-related diseases comprising the steps: (a) contacting Sirt7 protein with a test compound and an acetylated Sirt7 substrate; and (b) determining the level of the deacetylated Sirt7 substrate and/or the level of the acetylated Sirt7 substrate before contacting the protein with the test compound and after contacting the protein with the test compound wherein a reduced level of acetylated Sirt7 substrate or an increased level of deacetylated Sirt7 substrate after contacting the protein with the test compound as compared to the level before contacting the protein with the test compound indicates that the test compound is a compound useful in the treatment of age-related diseases or as a lead compound for the development of an agent for treating age-related diseases.
Since Sirt7 is, as described hereinabove, involved in processes that regulate ageing, its use as a target for the discovery of compounds that interfere with the processes of ageing is also envisaged by the present invention. Preferably, these compounds activate translation and/or enzymatic activity of Sirt7 in order to increase the level of physiologically active protein. Sirt7 protein is useful, as has been surprisingly found in accordance with the present invention, for the prevention of several diseases which are related to ageing, as is evident from the phenotypic alterations observed in Sirt7−/− mice (see Example 1 in connection with Examples 3 and 4) and therefore, increase of its expression level by the use of compounds identified in the above-described screen will result in amelioration or even loss of symptoms associated with said diseases.
In another aspect, the increase of enzymatic activity of Sirt7 by compounds identified as described above is also of use in the treatment of age-related diseases since an increased enzymatic activity leads to an increased substrate turnover rate which consequently leads to a reduction of active effector molecules such as p53. This is demonstrated in the reduction of active p53 by deacetylation via Sirt7 in vitro (Example 2). It is known that p53 is involved in premature ageing phenotypes (Gentry and Venkatachalam, Aging Cell, 2005: 4, 157). In Sirt7−/− mice, p53 was found to be in its active (acetylated) state. Therefore, it is evident that a higher turnover rate of p53 from its acetylated into its deacetylated (inactive) state will lead to reduction of the negative effects caused by active p53. As the applicant does not wish to be bound by any theory, also other mechanisms of action of Sirt7 via other (known or not yet known) effector molecules are within the scope of the present invention.
A “compound” in accordance with the present invention is, for example, a small molecule. Such a small molecule may be, for example, an organic molecule. Organic molecules relate or belong to the class of chemical compounds having a carbon basis, the carbon atoms linked together by carbon-carbon bonds. The original definition of the term organic related to the source of chemical compounds, with organic compounds being those carbon-containing compounds obtained from plant or animal or microbial sources, whereas inorganic compounds were obtained from mineral sources. Organic compounds can be natural or synthetic. Alternatively the compound may be an inorganic compound. Inorganic compounds are derived from mineral sources and include all compounds without carbon atoms (except carbon dioxide, carbon monoxide and carbonates).
The “acetylated Sirt7 substrate” in accordance with the present invention includes but is not limited to p53, FOXO, NFkB, p300, MyoD or the neuronal bHLH proteins NSCL1 and NSCL2. Also included are, for example, histone H3 and H4, Ku-70, PVAF, PGC-1α and PPARγ.
The determination of the level of acetylated or deacetylated Sirt7 substrate is accomplished by methods including but not limited to Western blot analysis, reverse-phase HPLC, Charcoal-binding assays or thin-layer-chromatography assays. For Western Blot analysis antibodies can be used that recognize the acetylated form of the substrate or, alternatively, the substrate may be immunoprecipitated and the acetylation level detected using an antibody against acetylated lysine. Using radiolabeled acetylated substrates, SDS/PAGE gels can also be dried and exposed to photographic film, after which the loss of radioactivity on the substrate can be visualized. Alternatively, the reaction mixture can be spotted onto a Whatman P81 cation exchange paper, which traps the radiolabeled, acetylated protein substrate. After extensive washing, the paper is subjected to scintillation counting, and a decrease in the counts reflects the level of deacetylation. Analysis by reverse-phase HPLC relies on the separation of substrates and products of the deacetylase reaction. Quenched reaction mixtures are injected onto a C18 column and, using a gradient of increased levels of organic solvent, substrates, products, and enzyme can be resolved. Charcoal-binding assays can be performed using 3H acetylated substrate. This assay takes advantage of the fact that under high pH and heat, the 3H acetyl group from 3H—O-acetyl-ADP-ribose (OAADPr) is hydrolysed. The 3H acetate does not bind to charcoal and can, therefore, be separated from the rest of the charcoal-bound substrates and products. Thin-layer-chromatography assays can be performed in presence of radiolabeled NAD+.
Substrate measurement is advantageous since it directly delivers a readout of the enzymatic activity of the investigated protein.
In a preferred embodiment, the Sirt7 substrate is p53.
P53 deacetylation is suitable as a readout for assessing the age-suppressing properties of various compounds since, as surprisingly discovered in the present invention, Sirt7 efficiently deacetylates p53.
In a more preferred embodiment, the method is carried out in vitro.
In vitro methods offer the possibility of establishing high-throughput assays which are capable of screening up to several thousand compounds in parallel. High-throughput assays, independently of being biochemical, cellular or other assays, generally may be performed in wells of microtiter plates, wherein each plate may contain 96, 384 or 1536 wells. Handling of the plates, including incubation at temperatures other than ambient temperature, and bringing into contact of test compounds with the assay mixture is preferably effected by one or more computer-controlled robotic systems including pipetting devices. In case large libraries of test compounds are to be screened and/or screening is to be effected within short time, mixtures of, for example 10, 20, 30, 40, 50 or 100 test compounds may be added to each well. In case a well exhibits biological activity, said mixture of test compounds may be de-convoluted to identify the one or more test compounds in said mixture giving rise to said activity.
The identified so-called lead compounds may be optimized to arrive at a compound which may be, for example, used in a pharmaceutical composition. Methods for the optimization of the pharmacological properties of compounds identified in screens, the lead compounds, are known in the art and comprise methods of modifying a compound identified as a lead compound to achieve: (i) modified site of action, spectrum of activity, organ specificity, and/or (ii) improved potency, and/or (iii) decreased toxicity (improved therapeutic index), and/or (iv) decreased side effects, and/or (v) modified onset of therapeutic action, duration of effect, and/or (vi) modified pharmacokinetic parameters (resorption, distribution, metabolism and excretion), and/or (vii) modified physico-chemical parameters (solubility, hygroscopicity, color, taste, odor, stability, state), and/or (viii) improved general specificity, organ/tissue specificity, and/or (ix) optimized application form and route by (i) esterification of carboxyl groups, or (ii) esterification of hydroxyl groups with carboxylic acids, or (iii) esterification of hydroxyl groups to, e.g. phosphates, pyrophosphates or sulfates or hemi-succinates, or (iv) formation of pharmaceutically acceptable salts, or (v) formation of pharmaceutically acceptable complexes, or (vi) synthesis of pharmacologically active polymers, or (vii) introduction of hydrophilic moieties, or (viii) introduction/exchange of substituents on aromates or side chains, change of substituent pattern, or (ix) modification by introduction of isosteric or bioisosteric moieties, or (x) synthesis of homologous compounds, or (xi) introduction of branched side chains, or (xii) conversion of alkyl substituents to cyclic analogues, or (xiii) derivatisation of hydroxyl group to ketales, acetales, or (xiv) N-acetylation to amides, phenylcarbamates, or (xv) synthesis of Mannich bases, imines, or (xvi) transformation of ketones or aldehydes to Schiff's bases, oximes, acetales, ketales, enolesters, oxazolidines, thiazolidines or combinations thereof.
The various steps recited above are generally known in the art. They include or rely on quantitative structure-activity relationship (QSAR) analyses (Kubinyi, “Hausch-Analysis and Related Approaches”, VCH Verlag, Weinheim, 1992), combinatorial biochemistry, classical chemistry and others (see, for example, Holzgrabe and Bechtold, Deutsche Apotheker Zeitung 2000, 140(8): 813).
In a more preferred embodiment, the age related diseases are selected from the group consisting of fibrosis, inflammatory cardiomyopathy, heart hypertrophy, liver degeneration, skeletal muscle degeneration, chronic general inflammation.
As described hereinabove, Fibrosis generally relates to the formation of scar tissue in organs such as the liver or the heart. Inflammatory cardiomyopathy relates to an abnormal heart condition in which the heart is dilated (poor pumping power), restrictive (impaired ability of the heart to fill) or hypertrophic (enlarged heart). Heart hypertrophy is a disorder in which the heart muscle is so strong that it does not relax enough to fill the heart with blood and so has reduced pumping ability. Skeletal muscle degeneration generally refers to muscle wasting, sarcopenia as well as depletion of muscular tissues and fat stores. Chronic general inflammation generally relates to an infiltration of organs with inflammatory cells such as macrophages and neutrophile lymphocytes as well as increased levels of CRP and IL6. Emerging pathological evidence indicates that major chronic ageing-related diseases such as atherosclerosis, arthritis, dementia, osteoporosis and cardiovascular diseases are inflammation-related.
In another embodiment, the invention relates to a method for the identification of a compound useful in the treatment of age-related diseases or as a lead compound for the development of an agent for treating age-related diseases comprising the steps: (a) determining the level of Sirt7 transcript or protein in a cell wherein said cell comprises inducible Sirt7 DNA; (b) contacting said cell with a test compound; (c) determining the level of Sirt7 transcript or protein in said cell after contacting with the test compound; and (d) comparing the Sirt7 transcript or protein level determined in step (c) with the Sirt7 transcript or protein level determined in step (a) wherein an increase of Sirt7 transcript or protein level in step (c) as compared to step (a) indicates that the test compound is a compound useful in the treatment of age-related diseases or as a lead compound for the development of an agent for treating age-related diseases.
The term “inducible” in accordance with the present invention refers to an increase of Sirt7 transcript or protein levels in a cell, wherein this increase is a result of the induction of Sirt7 expression by the test compound. The “inducible Sirt7 DNA” may, for example, be the endogenous Sirt7 gene with it's naturally occurring Sirt7 promoter. Alternatively, the cell may be transfected with a construct comprising the Sirt7 gene and the naturally occurring promoter-active DNA fragments which are located in the 5′-flanking region of the gene and which are sufficient for transcriptional control of the Sirt7 gene. The level of Sirt7 transcript or protein may e.g. be undetectable before contacting the above-mentioned cell with the test compound and it may be clearly detectable after contacting the cell with the test compound in order to indicate a compound suitable for the treatment of age-related diseases or as a lead compound for the development of a compound for the treatment of age-related diseases. Alternatively, the above-mentioned cell may exhibit a detectable level of Sirt7 transcript or protein before contacting with the test compound and the level of Sirt7 transcript or protein may be higher after contacting the cell with the test compound. Preferably, the level of Sirt7 transcript or protein is for example at least 5, 10, 20, 30, 40 or 50% higher after contacting the cell with the test compound. More preferably, the level of Sirt7 transcript or protein is for example at least 100, 200, 300 or 400% higher after contacting the cell with the test compound. Most preferably, the level of Sirt7 transcript or protein is for example at least 500% higher after contacting the cell with the test compound.
As described hereinabove, besides the enhancement of enzymatic activity, also the increase of expression levels conferred by a compound may contribute to the age-suppressing activity of said compound. Accordingly, measurement of the transcript or protein level of Sirt7 is another approach to determine the readout of the above-described assay. The measurement of the protein level can be accomplished in several ways. Western blotting or polyacrylamide gel electrophoresis in conjunction with protein staining techniques such as, but not limited to, Coomassie Brilliant blue or silver-staining may be used. Also of use in protein quantification is the Agilent Bioanalyzer technique.
Techniques for the determination of the transcript level include, but are not limited to RT-PCR and its various modifications such as qRT-PCR (also referred to as Real Time RT-PCR). PCR is well known in the art and is employed to make large numbers of copies of a target sequence. This is done on an automated cycler device, which can heat and cool containers with the reaction mixture in a very short time. The PCR, generally, consists of many repetitions of a cycle which consists of: (a) a denaturing step, which melts both strands of a DNA molecule and terminates all previous enzymatic reactions; (b) an annealing step, which is aimed at allowing the primers to anneal specifically to the melted strands of the DNA molecule; and (c) an extension step, which elongates the annealed primers by using the information provided by the template strand. Generally, PCR can be performed for example in a 50 μl reaction mixture containing 5 μl of 10×PCR buffer with 1.5 mM MgCl2, 200 μM of each deoxynucleoside triphosphate, 0.5 μl of each primer (10 μM), about 10 to 100 ng of template DNA and 1 to 2.5 units of Taq Polymerase. The primers for the amplification may be labeled or be unlabeled. DNA amplification can be performed, e.g., with a model 2400 thermal cycler (Applied Biosystems, Foster City, Calif.): 2 min at 94° C., followed by 30 to 40 cycles consisting of annealing (e.g. 30 s at 50° C.), extension (e.g. 1 min at 72° C., depending on the length of DNA template and the enzyme used), denaturing (e.g. 10 s at 94° C.) and a final annealing step at 55° C. for 1 min as well as a final extension step at 72° C. for 5 min. Suitable polymerases for use with a DNA template include, for example, E. coli DNA polymerase I or its Klenow fragment, T4 DNA polymerase, Tth polymerase, Taq polymerase, a heat-stable DNA polymerase isolated from Thermus aquaticus Vent, Amplitaq, Pfu and KOD, some of which may exhibit proof-reading function and/or different temperature optima. However, the person skilled in the art knows how to optimize PCR conditions for the amplification of specific nucleic acid molecules with primers of different length and/or composition or to scale down or increase the volume of the reaction mix. The “reverse transcriptase polymerase chain reaction” (RT-PCR) is used when the nucleic acid to be amplified consists of RNA. The term “reverse transcriptase” refers to an enzyme that catalyzes the polymerization of deoxyribonucleoside triphosphates to form primer extension products that are complementary to a ribonucleic acid template. The enzyme initiates synthesis at the 3′-end of the primer and proceeds toward the 5′-end of the template until synthesis terminates. Examples of suitable polymerizing agents that convert the RNA target sequence into a complementary, copy-DNA (cDNA) sequence are avian myeloblastosis virus reverse transcriptase and Thermus thermophilus DNA polymerase, a thermostable DNA polymerase with reverse transcriptase activity marketed by Perkin Elmer. Typically, the genomic RNA/cDNA duplex template is heat denatured during the first denaturation step after the initial reverse transcription step leaving the DNA strand available as an amplification template. High-temperature RT provides greater primer specificity and improved efficiency. U.S. patent application Ser. No. 07/746, 121, filed Aug. 15, 1991, describes a “homogeneous RT-PCR” in which the same primers and polymerase suffice for both the reverse transcription and the PCR amplification steps, and the reaction conditions are optimized so that both reactions occur without a change of reagents. Thermus thermophilus DNA polymerase, a thermostable DNA polymerase that can function as a reverse transcriptase, can be used for all primer extension steps, regardless of template. Both processes can be done without having to open the tube to change or add reagents; only the temperature profile is adjusted between the first cycle (RNA template) and the rest of the amplification cycles (DNA template). The RT Reaction can be performed, for example, in a 20 μl reaction mix containing: 4 μl of 5×AMV-RT buffer, 2 μl of Oligo dT (100 μg/ml), 2 μl of 10 mM dNTPs, 1 μl total RNA, 10 Units of AMV reverse transcriptase, and H2O to 20 μl final volume. The reaction may be, for example, performed by using the following conditions: The reaction is held at 70 C.° for 15 minutes to allow for reverse transcription. The reaction temperature is then raised to 95 C.° for 1 minute to denature the RNA-cDNA duplex. Next, the reaction temperature undergoes two cycles of 95° C. for 15 seconds and 60 C.° for 20 seconds followed by 38 cycles of 90 C.° for 15 seconds and 60 C.° for 20 seconds. Finally, the reaction temperature is held at 60 C.° for 4 minutes for the final extension step, cooled to 15 C.°, and held at that temperature until further processing of the amplified sample. Any of the above mentioned reaction conditions may be scaled up according to the needs of the particular case.
Real-time PCR employs a specific probe, in the art also referred to as TaqMan probe, which has a reporter dye covalently attached at the 5′ end and a quencher at the 3′ end. After the TaqMan probe has been hybridized in the annealing step of the PCR reaction to the complementary site of the polynucleotide being amplified, the 5′ fluorophore is cleaved by the 5′ nuclease activity of Taq polymerase in the extension phase of the PCR reaction. This enhances the fluorescence of the 5′ donor which was formerly quenched due to the close proximity to the 3′ acceptor in the TaqMan probe sequence. Thereby, the process of amplification can be monitored directly and in real time, which permits a significantly more precise determination of expression levels than conventional end-point PCR. Also of use in Real time RT-PCR experiments is a DNA intercalating dye such as SybrGreen for monitoring the de novo synthesis of double stranded DNA molecules.
In a more preferred embodiment, said cell is a primary cell or primary cell line. Primary cells are cells which are directly obtained from an organism. Suitable primary cells are, for example, mouse embryonic fibroblasts, mouse primary hepatocytes, cardiomyocytes and neuronal cells as well as mouse muscle stem cells (satellite cells) and stable, immortalized cell lines derived thereof. Also within the scope of the present invention are mammalian cells such as Hela, HEK293, H9 and Jurkat cells, NIH3T3 and C127 cells, Cos 1, Cos 7 and CV1, QC1-3 cells, mouse. L cells, mouse C2C12 cells and Chinese hamster ovary (CHO) cells.
In another more preferred embodiment said cell comprises a nucleic acid molecule encoding a protein having Sirt7 function fused to a reporter gene wherein said nucleic acid molecule (a) has the sequence of SEQ ID NO: 1, 3, 5 or 7; (b) encodes a protein having the sequence of SEQ ID NO: 2, 4, 6 or 8; (c) hybridizes under stringent conditions to the molecule of (a) or (b); or (d) has an identity on the nucleic acid level of at least 80% with the molecule of (a), (b) or (c).
The fusion to a reporter gene allows the indirect measurement of protein level by measuring the level of the reporter gene attached to the protein of interest. Examples of reporter genes include, but are not limited to, green fluorescent protein (GFP), yellow fluorescent protein (YFP), red fluorescent protein (RFP), cyan fluorescent protein (CFP), luciferase or β-galactosidase.
In another embodiment, the invention relates to a method of treating a subject suffering from an age-related disease by administering to said subject a pharmaceutical composition comprising (i) a nucleic acid molecule encoding a protein having Sirt7 function wherein said nucleic acid molecule (a) has the sequence of SEQ ID NO: 1, 3, 5 or 7; (b) encodes a protein having the sequence of SEQ ID NO: 2, 4, 6 or 8; (c) hybridizes under stringent conditions to the molecule of (a) or (b); or (d) has an identity on the nucleic acid level of at least 80% with the molecule of (a), (b) or (c); (ii) a vector comprising the nucleic acid molecule of (i); (iii) a host cell comprising the vector of (ii); or (iv) a protein encoded by the nucleic acid molecule of (i).
In a more preferred embodiment, the age related diseases are selected from the group consisting of fibrosis, inflammatory cardiomyopathy, heart hypertrophy, liver degeneration, skeletal muscle degeneration, chronic general inflammation.
As described hereinabove, Fibrosis generally relates to the formation of scar tissue in organs such as the liver or the heart. Inflammatory cardiomyopathy relates to an abnormal heart condition in which the heart is dilated (poor pumping power), restrictive (impaired ability of the heart to fill) or hypertrophic (enlarged heart). Heart hypertrophy is a disorder in which the heart muscle is so strong that it does not relax enough to fill the heart with blood and so has reduced pumping ability. Skeletal muscle degeneration generally refers to muscle wasting, sarcopenia as well as depletion of muscular tissues and fat stores. Chronic general inflammation generally relates to an infiltration of organs with inflammatory cells such as macrophages and neutrophile lymphocytes as well as increased levels of CRP and IL6. Emerging pathological evidence indicates that major chronic ageing-related diseases such as atherosclerosis, arthritis, dementia, osteoporosis and cardiovascular diseases are inflammation-related.
In a most preferred embodiment, the subject is a mammal, preferably a human.
The Figures show:
The Examples illustrate the invention:
Sirt7 knockout and overexpressing mice were generated as described in Example 1. Knockout animals were back-crossed to C57Bl/6 mouse strain and the transgenics to the ICR strain for at least four generations to ensure the same genetic background for control and mutant animals. No phenotypic differences were present in the first generation animals on mixed C57Bl/6; 129Sv background, which were used for some initial analyses. For all studies male littermates, which were kept under the same conditions, were used.
Mouse embryonic fibroblasts (MEFs) and primary liver hepatocytes were cultured under standard conditions as described in Braun et al. Cell 1992, 71: 369. Primary hepatocytes were isolated from perfused livers according to Seglen, P. O. Methods Cell Biol. 1976, 13: 29.
Deacetylation activity of recombinant mouse Sirt1 and Sirt7 protein was estimated using acetylated p53 peptides (p53-382/diAc) and Sirt1 Fluorometric Drug Discovery Kit—AK-555, BIOMOL according to manufacturers protocol.
Apoptotic cardiomyocytes on heart tissue sections were visualized using TUNEL staining and analyzed by confocal laser scanning microscopy. Apoptosis in cultured MEFs was measured by Cell Death Detection ELISA (Roche).
Magnetic Resonance Imaging was performed under volatile isoflurane (2%) anesthesia with a 7.05 T (Bruker) MR scanner equipped with a 300 mT/m gradient system, which works 300.51 MHz for isotope 1H. A 2.6 cm usable diameter quadrature low-pass birdcage coil was constructed in-house (Wagner et al. NMR Biomed. 2004, 17: 21) and used in all experiments. MRI experiments were performed by applying an ECG-triggered gradient-echo sequence with the following imaging parameters: echo time (TE)=2.9 ms; repetition time (TR)=128.5 ms; field of view (FOV)=4.00×4.00 cm2; acquisition matrix=129×256; maximal in-plane resolution=156×312 mm2; slice thickness=1.0 mm. One four-chamber view was obtained for each heart.
Blood cells were characterized by standard flow cytometry as described (Schulze et al. Genes Dev. 2005, 19: 1787) using PE- or FITC-conjugated antibodies against CD3, CD4, CD8, CD11b, CD19, and CD45. Data collected from >10,000 cells were expressed as the percentage of positive cells per total gated cells. Raw data were analyzed using the CellQuest pro software (BD Inc.).
Whole heart tissue or cell culture lysates were used. Cultures were washed three times with HBSS and lysed at the indicated time in Laemmli buffer containing 0.2M PMSF, 1M Na3VO4, 1M NaF, 1 mg/ml Aprotinin and Leupeptin (all from Sigma). 10 mg of protein lysates were separated on 4%-12% SDS-PAGE gradient gels and transferred onto nitrocellulose membranes (Invitrogen Life technologies, Groningen, The Netherlands). Immunoreactive proteins were visualized with corresponding HRP-conjugated secondary antibodies on Hyperfilm (GE Healthcare) using the SuperSignal West Pico or West Femto detection solutions (Perbio Science). Blots were scanned using a STORM 860 (Molecular Dynamics, Freiburg, Germany) and analyzed using ImageQuant software (Molecular Dynamics). Antibodies directed against p-PTEN, total PTEN, pAkt, total Akt, Ras, pan-actin, Fas/CD95 were from NEB (Cell Signalling) and c-Raf was from Becton Dickinson.
Tissues for immunochistochemistry were fixed and either embedded in paraffin or shock-frozen for cryosectioning, or processed for electron microscopy applying standard procedures (Oustanina et al. EMBO J. 2004, 23: 3430). The following antibodies were used: MF20, anti-γ-Sarcoglycan, anti-CollagenVl (Rockland), anti-CD68 (Dako), anti-SM-α-actin-antibody (Cymbus Biotechnology). Secondary antibodies were coupled with Alexa 596 (red), Alexa 350 (blue), and Alexa 488 (green) and used according to the manufacturer's instructions (Molecular Probes). Nuclei were visualized using a 30 μmolar DAPI solution (Molecular probes).
RNA was isolated using established procedures that have been described previously (Braun et al. Cell 1992, 71: 369). Quantitative RT PCR was achieved by cDNA amplification in the presence of the DNA-binding dye SYBR GreenI as described previously (Neuhaus et al. Mol. Cell. Biol. 2003, 23: 6037). The following primer pairs were used:
The relative amount of mRNA was calculated using the formula: [SQtarget/SGHPRT]. Relative values obtained for mutant and wild type samples were compared to each other.
For glucose and insulin tolerance measurements mice were set under fasting conditions for 4 h. Samples of approximately 300 μl were collected at time points indicated in
The targeting vector to obtain Sirt7 knockout mice was constructed by insertion of a 2.5 kb Accl fragment derived from the 5″-region of the Sirt7 gene comprising the first three exons into the vector pK11 in front of a neomycin-resistance cassette, flanked by frt recognition sites for Flp-recombinase. A 15.5 kb SalI-BamHI fragment from the 3″-region of the Sirt7 gene was inserted behind the selection cassette to generate a 3′-homology fragment (
The Sirt7−/− mice had a reduced lifespan, most animals died between 10 and 13 months without any apparent cause of death. In contrast Sirt7 overexpressing animals showed no decrease in the life span (
p53 acetylated peptides were efficiently deacetylated by Sirt7 in vitro and Sirt7 dependent p53 deacetylation was stimulated by a polyphenolic compound, resveratrol, which has been previously thought to specifically induce the enzymatic activity of Sirt12 (
Sirt7 mutants are very sensitive to combined cold and starvation stress. Sirt7 deficient mice were not able to keep a constant body temperature and normal blood glucose concentrations under cold stress (4° C.) preceded by over night fasting and died during the first three hours of cold exposure when the body temperature dropped below 20° C. and the blood glucose concentration below 70 mg/dl (
Sirt7−/− mice suffer from hypertrophic, inflammatory cardiomyopathy. Staining with γ-sarcoglycan indicated an enlargement of the majority of cardiomyocytes with strong caliber variations reflecting ongoing cardiac remodelling (
Sirt7−/− mice developed an increased heart/body ratio by 2.5 months of age, inflammation and a higher rate of apoptosis (
Sirt7−/− mice showed a smaller size and leanness, which became apparent at around five months of age (
Whereas the applicants do not wish to be bound by any scientific theory, the model as outlined in
| Number | Date | Country | Kind |
|---|---|---|---|
| 07102070.5 | Feb 2007 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP08/01028 | 2/11/2008 | WO | 00 | 3/31/2010 |
