A novel isoform of sarcolemmal membrane-associated protein (SLMAP) is a component of the microtubule organizing centre

RM Guzzo, S Sevinc, M Salih… - Journal of cell …, 2004 - journals.biologists.com
RM Guzzo, S Sevinc, M Salih, BS Tuana
Journal of cell science, 2004journals.biologists.com
The microtubule organizing centre (MTOC) or the centrosome serves a crucial role in the
establishment of cellular polarity, organization of interphase microtubules and the formation
of the bipolar mitotic spindle. We have elucidated the genomic structure of a gene encoding
the sarcolemmal membrane-associated protein (SLMAP), which encodes a 91 kDa
polypeptide with a previously uncharacterized N-terminal sequence encompassing a
forkhead-associated (FHA) domain that resides at the centrosome. Anti-peptide antibodies …
The microtubule organizing centre (MTOC) or the centrosome serves a crucial role in the establishment of cellular polarity, organization of interphase microtubules and the formation of the bipolar mitotic spindle. We have elucidated the genomic structure of a gene encoding the sarcolemmal membrane-associated protein (SLMAP), which encodes a 91 kDa polypeptide with a previously uncharacterized N-terminal sequence encompassing a forkhead-associated (FHA) domain that resides at the centrosome. Anti-peptide antibodies directed against SLMAP N-terminal sequences showed colocalization with γ-tubulin at the centrosomes at all phases of the cell cycle. Agents that specifically disrupt microtubules did not affect SLMAP association with centrosomes. Furthermore, SLMAP sequences directed a reporter green fluorescent protein (GFP) to the centrosome, and deletions of the newly identified N-terminal sequence from SLMAP prevented the centrosomal targeting. Deletion-mutant analysis concluded that overall, structural determinants in SLMAP were responsible for centrosomal targeting. Elevated levels of centrosomal SLMAP were found to be lethal, whereas mutants that lacked centrosomal targeting inhibited cell growth accompanied by an accumulation of cells at the G2/M phase of the cell cycle.
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