Centromere protein B (CENP-B) is a centromeric DNA-binding protein that bin
ds to ct-satellite DNA at the 17 bp CENP-B box sequence. The binding of CEN
P-B, along with other proteins, to ct-satellite DNA sequences at the centro
mere, is thought to package the DNA into heterochromatin subjacent to the k
inetochore of mitotic chromosomes. To determine the importance of CENP-B to
kinetochore assembly and function, we generated a mouse null for the cenpB
gene. The deletion removed part of the promoter and the entire coding sequ
ence except for the carboxyl-terminal 35 amino acids of the CENP-B polypept
ide. Mice heterozygous or homozygous for the cenpB null mutation are viable
and healthy, with no apparent defect in growth and morphology. We have est
ablished mouse embryo fibroblasts from heterozygous and homozygous cenpB nu
ll littermates. Microscopic analysis, using immunofluorescence and electron
microscopy of the cultured cells, indicated that the centromere-kinetochor
e complex was intact and identical to control cells. Mitosis was identical
in fibroblasts derived from cenpB wild-type, heterozygous and null animals.
Our studies demonstrate that CENP-B is not required for the assembly of he
terochromatin or the kinetochore, or for completion of mitosis.