Accession Number:

ADA586051

Title:

De Novo Chromosome Copy Number Variation in Fanconi Anemia-Associated Hematopoietic Defects

Descriptive Note:

Annual rept. 1 Apr 2012-31 Mar 2013

Corporate Author:

RHODE ISLAND UNIV KINGSTON

Personal Author(s):

Report Date:

2013-04-01

Pagination or Media Count:

7.0

Abstract:

Fanconi anemia FA is a rare disease characterized by developmental defects, progressive bone marrow failure BMF and pronounced cancer susceptibility. The FA proteins and the major breast cancer susceptibility gene products BRCA1 and BRCA2 function cooperatively in the FA-BRCA pathway to repair damaged DNA. Recent studies have demonstrated that the FA-BRCA pathway plays an important role in the response of hematopoietic stem and progenitor cells to cellular stresses, and in particular oxidative stress caused by elevated levels of reactive oxygen species ROS. In our research proposal, we have hypothesized that the FA-BRCA pathway may play an important role in the prevention of genome-wide de novo copy number variation. Chromosome copy number variation refers to gains or losses of large 10 kb genomic DNA segments. While copy number variation is a feature of normal genetic variation it is also strongly associated with genetic disease, including autism and psychiatric disorders. In addition, several recent studies have demonstrated that hematological malignancies show large numbers of de novo somatically acquired copy number variants CNVs.

Subject Categories:

  • Medicine and Medical Research

Distribution Statement:

APPROVED FOR PUBLIC RELEASE