Sfi1p has conserved centrin-binding sites and an essential function in budding yeast spindle pole body duplication

JV Kilmartin - The Journal of cell biology, 2003 - rupress.org
JV Kilmartin
The Journal of cell biology, 2003rupress.org
Centrins are calmodulin-like proteins present in microtubule-organizing centers. The
Saccharomyces cerevisiae centrin, Cdc31p, was functionally tagged with a single Z domain
of protein A, and used in pull-down experiments to isolate Cdc31p-binding proteins. One of
these, Sfi1p, localizes to the half-bridge of the spindle pole body (SPB), where Cdc31p is
also localized. Temperature-sensitive mutants in SFI1 show a defect in SPB duplication and
genetic interactions with cdc31-1. Sfi1p contains multiple internal repeats that are also …
Centrins are calmodulin-like proteins present in microtubule-organizing centers. The Saccharomyces cerevisiae centrin, Cdc31p, was functionally tagged with a single Z domain of protein A, and used in pull-down experiments to isolate Cdc31p-binding proteins. One of these, Sfi1p, localizes to the half-bridge of the spindle pole body (SPB), where Cdc31p is also localized. Temperature-sensitive mutants in SFI1 show a defect in SPB duplication and genetic interactions with cdc31-1. Sfi1p contains multiple internal repeats that are also present in a Schizosaccharomyces pombe protein, which also localizes to the SPB, and in several human proteins, one of which localizes close to the centriole region. Cdc31p binds directly to individual Sfi1 repeats in a 1:1 ratio, so a single molecule of Sfi1p binds multiple molecules of Cdc31p. The centrosomal human protein containing Sfi1 repeats also binds centrin in the repeat region, showing that this centrin-binding motif is conserved.
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