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Vol. 12, Issue 11, 3527-3537, November 2001






§
Departments of *Molecular and Cellular Biology,
Condensin is a conserved 13S heteropentamer composed of two
nonidentical structural maintenance of chromosome (SMC) family proteins, in Xenopus XCAP-C and XCAP-E, and three
regulatory subunits, XCAP-D2, XCAP-G, and XCAP-H. Both biochemical and
genetic analyses have demonstrated an essential role for the 13S
condensin complex in mitotic chromosome condensation. Further, a
potential requirement for condensin in completion of chromatid arm
separation in early anaphase is demonstrated by the mutational
phenotypes of the Drosophila homologues of
XCAP-H, barren and XCAP-C,
DmSMC4. In this study we have investigated the
expression and subcellular distribution of hCAP-H, the human homolog of
XCAP-H, in order to better understand its cellular functions.
Transcription of hCAP-H was restricted to proliferating
cells with highest expression during the G2 phase of the
cell cycle. In contrast, cellular hCAP-H protein levels were constant
throughout the cell cycle. hCAP-H was found to be associated with
mitotic chromosomes exhibiting a nonuniform but symmetric distribution
along sister chromatids. The symmetry of hCAP-H association with sister
chromatids suggests that there are sequence-dependent domains of
condensin aggregation. During interphase hCAP-H, -C, and -E, have
distinct punctate nucleolar localization, suggesting that condensin may
associate with and modulate the conformation and function of rDNA.
hCAP-H association with condensed chromatin was not observed in the
early phase of chromosome condensation when histone H3 phosphorylation
has already taken place. This finding is consistent with the hypothesis
that histone H3 phosphorylation precedes condensin-mediated condensation.
Molecular and Human Genetics,
Pediatrics,
and §Immunology, Baylor College of Medicine, One Baylor
Plaza, Houston, Texas 77030
Corresponding author. E-mail address:
jbelmont{at}bcm.tmc.edu.
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