The regulation of sister-chromatid segregation in Drosophila will be analyzed. While disjunction of sister-chromatids is common to both meiosis and mitosis, in meiosis sister-chromatid separation occurs in meiosis II and is inhibited in meiosis I. Thus there are functions that promote sister-chromatid cohesion as well as those that lead to disjunction. Two Drosophila mutants, mei-S332 and ord, result in precocious sister-chromatid separation in meiosis I of both males and females, providing a key to unraveling this process. We have recently isolated additional alleles of each of these loci; these alleles reveal that the mei-S332 is not required to maintain sister-chromatid cohesion until anaphase I, after the kinetochore has duplicated. The new alleles of mei-S332 will be analyzed for their effects on sister-chromatid segregation in meiosis and mitosis using genetic and cytological approaches. The mei-S332 gene will be cloned and its products identified and characterized. Since an interesting possibility is that the gene encodes a component of the kinetochore which functions to maintain cohesion or the two duplicated halves, the cytological location of the mei-S332 gene product will be analyzed. Sister-chromatid disjunction is central to the ordered segregation of chromosomes is eukaryotic organisms. The information resulting from this work will allow us to understand better fundamental aspect of inheritance.

Agency
National Science Foundation (NSF)
Institute
Division of Molecular and Cellular Biosciences (MCB)
Application #
9020672
Program Officer
DeLill Nasser
Project Start
Project End
Budget Start
1991-04-01
Budget End
1994-09-30
Support Year
Fiscal Year
1990
Total Cost
$326,584
Indirect Cost
Name
Whitehead Institute for Biomedical Research
Department
Type
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02142