ISSN:
1573-6849
Keywords:
autoantigen
;
centromere
;
cross-linking
;
dimerization
;
kinetochore
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
Notes:
Abstract Human centromere protein C (CENP-C), a chromosomal component of the inner plate of kinetochores, was originally identified as one of the centromere auto-antigens. In a previous study, we showed that it possesses DNA-binding activity in vitro. Recently, centromere-binding activity was suggested at the C-terminal region in vivo. However, little is known about the role of CENP-C in kinetochore organization. Here, to characterize its biochemical properties, three separate antigenic regions of human CENP-C were expressed in Escherichia coli, affinity purified and used in South-western blotting and chemical cross-linking analyses. We found that the internal DNA-binding domain was composed of two kinds of elements: the ‘core’ and two flanking ‘stabilizing’ elements that support the activity. When cross-linked with disuccinimidyl suberate (DSS), the N-terminal region produced the ladder bands of dimerand tetramer: the C-terminal region exclusively produced the dimer band, whereas the internal region was not affected at all. Dimer formation at the C-terminus in the native state was also indicated by gel filtration and the presence of conformation-specific autoantibodies in the patient's sera. These results suggest that human CENP-C consists of three functional units required for ‘kinetochore assembly’: a putative N-terminal oligomerization domain, an internal DNA-binding domain and a C-terminal dimerization domain.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1023/A:1018422325569
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