Collaborative Research: Illumination of Smc5/6 management of DNA repair intermediate structures

Information

  • NSF Award
  • 2414613
Owner
  • Award Id
    2414613
  • Award Effective Date
    7/1/2024 - 4 months ago
  • Award Expiration Date
    6/30/2027 - 2 years from now
  • Award Amount
    $ 166,688.00
  • Award Instrument
    Continuing Grant

Collaborative Research: Illumination of Smc5/6 management of DNA repair intermediate structures

The massive amounts of genomic DNA in the cell must undergo major structural transformations when genetic information is replicated or repaired. During these processes, branch-shaped DNA structures are formed as intermediates and then are processed into linear DNA products. Many protein factors collaborate during the formation and processing of different types of branched DNA structures. How many of these proteins interact with branched DNAs and enable their processing is not clear. The objective of this collaborative project is to determine how a genome-protecting complex called Smc5/6 manages various branched DNA structures. The two research teams will combine biochemical and biophysical expertise to achieve high-resolution understanding of Smc5/6 structure and function. The outcomes will advance knowledge of how cells quickly resolve DNA repair intermediates to ensure genome integrity. In addition, the project will have educational impact through workshops that cultivate interest in DNA and genome research among middle-high school students and teachers, as well as interdisciplinary research training opportunities for undergraduate and graduate students.<br/> <br/>Smc5/6 is emerging as an important and highly conserved protein complex that is required for the processing of DNA repair intermediates. However, the mechanism of action of Smc5/6, including its interactions with branched DNA structures is poorly understood. This study will provide critical insights into the molecular functions of Smc5/6. Specifically, the two research teams will examine how Smc5/6 recognizes Holliday junction recombinational repair intermediates and R-loop RNA-DNA hybrid structures, using complementary biochemical and high-speed atomic force microscopy (HS-AFM) methodologies. In addition, HS-AFM imaging will be used to directly observe the sequential steps whereby DNA helicases resolve these structures and how Smc5/6 affects these steps. By integrating dynamic HS-AFM data with biochemical data, the project has potential to provide novel insights into DNA repair. Given the importance of Smc5/6 in genome maintenance and its evolutionary conservation in eukaryotes, this new knowledge could illuminate DNA repair mechanisms in diverse organisms.<br/><br/>This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

  • Program Officer
    Manju Hingoranimhingora@nsf.gov7032927323
  • Min Amd Letter Date
    6/25/2024 - 5 months ago
  • Max Amd Letter Date
    6/25/2024 - 5 months ago
  • ARRA Amount

Institutions

  • Name
    Sloan Kettering Institute For Cancer Research
  • City
    NEW YORK
  • State
    NY
  • Country
    United States
  • Address
    1275 YORK AVE
  • Postal Code
    100656007
  • Phone Number
    6462273273

Investigators

  • First Name
    Xiaolan
  • Last Name
    Zhao
  • Email Address
    zhaox1@mskcc.org
  • Start Date
    6/25/2024 12:00:00 AM

Program Element

  • Text
    Genetic Mechanisms
  • Code
    111200

Program Reference

  • Text
    NANOSCALE BIO CORE
  • Code
    7465