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Overexpression of spindlin1 induces metaphase arrest and chromosomal instability
Author(s) -
Zhang Peng,
Cong Bin,
Yuan Hongfeng,
Chen Lin,
Lv Yang,
Bai Cixian,
Nan Xue,
Shi Shuangshuang,
Yue Wen,
Pei Xuetao
Publication year - 2008
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.21515
Subject(s) - mitosis , microbiology and biotechnology , mad2 , multipolar spindles , metaphase , biology , anaphase , spindle checkpoint , chromosome segregation , chromosome instability , spindle apparatus , prometaphase , kinetochore , spindle pole body , plk1 , cell cycle , cell division , chromosome , genetics , cell , gene
Spin/Ssty gene family is high conserved and very abundant transcript involved in gametogenesis, which was repeatedly detected in early embryo. Nevertheless, the biologic roles of the members are still largely unknown. Previously we have identified human gene spindlin1 as a homologue of the family from ovarian cancer cells, and reported that stable overexpression of spindlin1 could transform NIH3T3 cells and induce tumorigenesis in nude mouse. Here, we showed that spindlin1, as a nuclear protein, was relocated during mitosis. A fraction of spindlin1 proteins was dynamic distributed along mitotic spindle tubulin and enriched at midzone following anaphase entering. We also showed that transient overexpression of spindlin1 induced cell cycle delay in metaphase, caused mitotic spindle defects, and resulted in chromosome instability, micronucleus and multinuclear giant cells formation. Moreover, time‐lapse microscopy revealed that these cells arrested at metaphase for more than 3 h with chromosome nondisjunction or missegregation. Furthermore, Mad2 up‐regulation in these cells suggested that overexpression of spindlin1 may affect the bipolar spindle correctly attachment to chromosomes and activate spindle checkpoint. Taken together, these data demonstrated that excess spindlin1 protein may be detrimental for spindle microtubule organization, chromosomal stability and can potentially contribute to the development of cancer. J. Cell. Physiol. 217: 400–408, 2008. © 2008 Wiley‐Liss, Inc.