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Vol. 13, Issue 11, 3890-3900, November 2002

§ and
*Department of Biological Sciences, Dartmouth College, Hanover, New
Hampshire 03755-3576; and Cohesion between sister chromatids is a prerequisite for accurate
chromosome segregation during mitosis and meiosis. To allow chromosome
condensation during prophase, the connections that hold sister
chromatids together must be maintained but still permit extensive
chromatin compaction. In Drosophila, null mutations in
the orientation disruptor (ord) gene
lead to meiotic nondisjunction in males and females because cohesion is
absent by the time that sister kinetochores make stable
microtubule attachments. We provide evidence that ORD is concentrated
within the extrachromosomal domains of the nuclei of
Drosophila primary spermatocytes during early G2, but
accumulates on the meiotic chromosomes by mid to late G2. Moreover,
using fluorescence in situ hybridization to monitor cohesion directly,
we show that cohesion defects first become detectable in
ordnull spermatocytes shortly after
the time when wild-type ORD associates with the chromosomes. After
condensation, ORD remains bound at the centromeres of wild-type
spermatocytes and persists there until centromeric cohesion is released
during anaphase II. Our results suggest that association of ORD with
meiotic chromosomes during mid to late G2 is required to maintain
sister-chromatid cohesion during prophase condensation and that
retention of ORD at the centromeres after condensation ensures the
maintenance of centromeric cohesion until anaphase II.
Department of Biology,
Massachusetts Institute of Technology and Whitehead Institute,
Cambridge, Massachusetts 02142
Present address: Department of Molecular,
Cellular, and Developmental Biology, University of South Carolina, 700 Sumter Street, Columbia, SC 29205.
§
Present address: Department of Molecular and
Cellular Biology, 401 Baker Hall #3204, University of
California, Berkeley, CA 94720.
Corresponding author. E-mail address:
s.bickel{at}dartmouth.edu.
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