Journal of Cell Science 115, e1405-e1405 (2002)
© 2002 The Company of Biologists Limited
Chromosome condensation: maternal and paternal differences
Condensation of chromosomes is essential for mitosis and depends on their
recruitment of condensin complexes containing structural maintenance of
chromosomes (SMC) proteins and regulators such as CAP-D2. Is the condensation
mechanism always the same? In zygotes, condensed paternal chromosomes are less
compact than their maternal counterparts, but whether this reflects different
condensation mechanisms has never been clear. Philippe Collas and co-workers
now show that the condensation mechanisms of maternal and paternal chromosomes
in mitotic zygotes do indeed differ (see
p. 2931). They find that
AKAP95 a scaffold protein previously shown to recruit condensin to
chromatin is targeted to maternal chromosomes in the female pronucleus
but does not enter the male pronucleus. In addition, using peptides that
compete with AKAP95, the authors show that AKAP95 is required for recruitment
of CAP-D2 to and condensation of maternal but not paternal chromosomes. Collas
and co-workers conclude that an AKAP95-independent mechanism recruits
condensin during paternal chromosome condensation in zygotes, suggesting that
this could affect the degree of compaction of the condensed chromosomes.

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Related articles in JCS:
- Differential regulation of maternal and paternal chromosome condensation in mitotic zygotes
- Jacqueline Bomar, Pedro Moreira, John J. Balise, and Philippe Collas
JCS 2002 115: 2931-2940.
[Abstract]
[Full Text]