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Anindya  Dutta
Degree(s): M.D., Ph.D.
Graduate School: University of Madras; Rockefeller University
Primary Appointment: Professor of Biochemistry and Molecular Genetics
Research Interests:
DNA Replication and Genomic Instability in Cancer Cells

Email Address: ad8q@virginia.edu


Biomedical Sciences Graduate Program(s)
  • Biochemistry, Molecular Biology and Genetics
  • Molecular Medicine
  • Microbiology, Immunology and Infectious Diseases

  • Research Description

    Our lab studies the genetics and genomics of the cell-cycle in normal and cancer cells with an emphasis on microRNAs, DNA replication and DNA damage. The projects in the lab are summarized below: (1) We have focused on microRNAs that regulate cell-cycle progression during muscle differentiation or in prostate cancers, with a special emphasis on potential tumor suppressor microRNAs. We discover microRNAs that change under specific conditions using techniques like microarrays and cloning/high-throughput sequencing and identify the targets of the relevant microRNAs. (2) A better knowledge of how DNA replication is initiated or regulated in mammalian cells will allow us to devise (or discover) inhibitors that restrain DNA replication in cancer cells and understand how disorders in their regulation lead to genomic instability. For example, we are the part of the ENCODE consortium that maps origins of replication in human cells using genome tiling arrays. We also study the regulation of replication initiation-factors like ORC, Cdt1, geminin and Mcm10, to understand how they initiate replication and regulate the normal cell-cycle. (3) We study how tumor suppressors are involved in the normal response of the cell to DNA damage arising from endogenous or exogenous sources. Thus, we have implicated tumor suppressor proteins like p53, Fanconi Anemia complex and BRCA1 in the response of a cell to DNA damage induced by re-replication.


    Selected Publications
  • ENCODE project consortium. The ENCODE pilot project: identification and analysis of functional elements in 1% of the human genome. Nature, 2007; 447:799-816.
  • Lee YS and Dutta A. The tumor suppressor microRNA let-7 represses the HMGA2 oncogene.  Genes & Development, 2007; 21:1025-30.

  • Kim HK, Lee YS, Sivaprasad U, Malhotra A and Dutta A. Muscle-specific microRNA miR-206 promotes muscle differentiation. J. Cell Biology 2006; 174, 677-687.
  • Machida YJ, Machida Y, Chen Y, Gurtan A, Kupfer GM, DíAndrea AD and Dutta A. UBE2T is the E2 in the Fanconi Anemia Pathway and Undergoes Negative Regulation by Autoubiquitination. Molecular Cell, 2006; 23, 589-96.
  • PubMed Listings for this Faculty Member

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    Contact Information
      Office Address: PO Box 800733, 
      Office Phone: +1 434-924-1227
      Web Site: http://mexico.bioch.virginia.edu/

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    http://mexico.bioch.virginia.edu

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