We have designed and utilized two in vivo assays of kinetochore integr
ity in S. cerevisiae. One assay detects relaxation of a transcription
block formed at centromeres; the other detects an increase in the mito
tic stability of a dicentric test chromosome. ctf13-30 and ctf14-42 we
re identified as putative kinetochore mutants by both assays. CTF14 is
identical to NDC10/CBF2, a recently identified essential gene that en
codes a 110 kd kinetochore component. CTF13 is an essential gene that
encodes a predicted 478 amino acid protein with no homology to known p
roteins. ctf13 mutants missegregate chromosomes at permissive temperat
ure and transiently arrest at nonpermissive temperature as large-budde
d cells with a G2 DNA content and a short spindle. Antibodies recogniz
ing epitope-tagged CTF13 protein decrease the electrophoretic mobility
of a CEN DNA-protein complex formed in vitro. Together, the genetic a
nd biochemical data indicate that CTF13 is an essential kinetochore pr
otein.