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Centromere Protein B of African Green Monkey Cells: Gene Structure, Cellular Expression, and Centromeric Localization

Overview
Journal Mol Cell Biol
Specialty Cell Biology
Date 1996 Sep 1
PMID 8756674
Citations 19
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Abstract

Centromere protein B (CENP-B) is a centromeric DNA-binding protein which recognizes a 17-bp sequence (CENP-B box) in human and mouse centromeric satellite DNA. The African green monkey (AGM) is phylogenetically closer to humans than mice and is known to contain large amounts of alpha-satellite DNA, but there has been no report of CENP-B boxes or CENP-B in the centromere domains of its chromosomes. To elucidate the AGM CENP-B-CENP-B box interaction, we have analyzed the gene structure, expression, biochemical properties, and centromeric localization of its CENP-B. The amino acid sequence deduced from the cloned AGM CENP-B gene was established to be highly homologous to that of human and mouse CENP-B. In particular, the DNA binding and homodimer formation domains demonstrated 100% identity to their human and mouse counterparts. Immunoblotting and DNA mobility shift analyses revealed CENP-B to be expressed in AGM cell lines. As predicted from the gene structure, the AGM CENP-B in the cell extracts exhibited the same DNA binding specificity and homodimer forming activity as human CENP-B. By indirect immunofluorescent staining of AGM mitotic cells with anti-CENP-B antibodies, a centromere-specific localization of AGM CENP-B could be demonstrated. We also isolated AGM alpha-satellite DNA with a CENP-B box-like sequence with CENP-B affinity. These results not only prove that CENP-B functionally persists in AGM cells but also suggest that the AGM genome contains the recognition sequences for CENP-B (CENP-B boxes with the core recognition sequence or CENP-B box variants) in centromeric satellite DNA.

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References
1.
Rattner J . The organization of the mammalian kinetochore: a scanning electron microscope study. Chromosoma. 1987; 95(3):175-81. DOI: 10.1007/BF00330348. View

2.
Yoda K, Kitagawa K, Masumoto H, Muro Y, Okazaki T . A human centromere protein, CENP-B, has a DNA binding domain containing four potential alpha helices at the NH2 terminus, which is separable from dimerizing activity. J Cell Biol. 1992; 119(6):1413-27. PMC: 2289762. DOI: 10.1083/jcb.119.6.1413. View

3.
El-Deiry W, Kern S, Pietenpol J, Kinzler K, Vogelstein B . Definition of a consensus binding site for p53. Nat Genet. 1992; 1(1):45-9. DOI: 10.1038/ng0492-45. View

4.
Goh P, Kilmartin J . NDC10: a gene involved in chromosome segregation in Saccharomyces cerevisiae. J Cell Biol. 1993; 121(3):503-12. PMC: 2119568. DOI: 10.1083/jcb.121.3.503. View

5.
Jiang W, Lechner J, Carbon J . Isolation and characterization of a gene (CBF2) specifying a protein component of the budding yeast kinetochore. J Cell Biol. 1993; 121(3):513-9. PMC: 2119569. DOI: 10.1083/jcb.121.3.513. View