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SPC25, NDC80 kinetochore complex component, homolog (S. cerevisiae) OKDB#: 4414
 Symbols: SPC25 Species: human
 Synonyms: AD024, SPBC25, hSpc25, MGC22228,  Locus: 2q31.1 in Homo sapiens


For retrieval of Nucleotide and Amino Acid sequences please go to: OMIM Entrez Gene
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General Comment NCBI Summary: This gene encodes a protein that may be involved in kinetochore-microtubule interaction and spindle checkpoint activity. [provided by RefSeq]
General function Chromosome organization
Comment
Cellular localization Nuclear
Comment
Ovarian function Oocyte maturation
Comment Spc25?-?How the kinetochore protein plays during oocyte meiosis. Xiong B et al. Comment on: Sun SC, et al. Cell Cycle 2010; 9:4552-9.
Expression regulated by
Comment
Ovarian localization Oocyte
Comment Perturbation of Spc25 expression affects meiotic spindle organization, chromosome alignment and spindle assembly checkpoint in mouse oocytes. Sun SC et al. Spc25 is a component of the Ndc80 complex which consists of Ndc80, Nuf2, Spc24 and Spc25. Previous work has shown that Spc25 is involved in regulation of kinetochore microtubule attachment and the spindle assembly checkpoint in mitosis. the roles of Spc25 in meiosis remain unknown. Here, we report its expression, localization and functions in mouse oocyte meiosis. The Spc25 mRNA level gradually increased from the GV to MI stage, but decreased by MII during mouse oocyte meiotic maturation. Immunofluorescent staining showed that Spc25 was restricted to the germinal vesicle, and associated with chromosomes during all stages after GVBD. Overexpression of Spc25 by mRNA injection resulted in oocyte meiotic arrest, chromosome misalignment and spindle disruption. Conversely, Spc25 RNAi by siRNA injection resulted in precocious polar body extrusion and caused severe chromosome misalignment and aberrant spindle formation. Our data suggest that Spc25 is required for chromosome alignment, spindle formation and proper spindle checkpoint signaling during meiosis.
Follicle stages Preovulatory
Comment
Phenotypes
Mutations 0 mutations
Genomic Region show genomic region
Phenotypes and GWAS show phenotypes and GWAS
Links
OMIM (Online Mendelian Inheritance in Man: an excellent source of general gene description and genetic information.)
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created: Nov. 24, 2010, 6:31 a.m. by: hsueh   email:
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last update: March 23, 2011, 9:19 a.m. by: hsueh    email:



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