Learning about cancer from frogs: analysis of mitotic spindles in Xenopus egg extracts
Author(s) -
Marie K. Cross,
Maureen A. Powers
Publication year - 2009
Publication title -
disease models and mechanisms
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.327
H-Index - 83
eISSN - 1754-8411
pISSN - 1754-8403
DOI - 10.1242/dmm.002022
Subject(s) - spindle checkpoint , spindle apparatus , biology , xenopus , mitosis , spindle pole body , microbiology and biotechnology , aneuploidy , multipolar spindles , kinetochore , microtubule , function (biology) , cancer , cell division , genetics , cell , gene , chromosome
The mitotic spindle is responsible for correctly segregating chromosomes during cellular division. Disruption of this process leads to genomic instability in the form of aneuploidy, which can contribute to the development of cancer. Therefore, identification and characterization of factors that are responsible for the assembly and regulation of the spindle are crucial. Not only are these factors often altered in cancer, but they also serve as potential therapeutic targets. Xenopus egg extract is a powerful tool for studying spindle assembly and other cell cycle-related events owing, in large part, to the ease with which protein function can be manipulated in the extract. Importantly, the spindle factors that have been characterized in egg extract are conserved in human spindle assembly. In this review, we explain how the extract is prepared and manipulated to study the function of individual factors in spindle assembly and the spindle checkpoint. Furthermore, we provide examples of several spindle factors that have been defined functionally using the extract system and discuss how these factors are altered in human cancer.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom