Xenopus tropicalis egg extracts provide insight into scaling of the mitotic spindle

被引:85
作者
Brown, Katherine S.
Blower, Michael D.
Maresca, Thomas J.
Grammer, Timothy C.
Harland, Richard M.
Heald, Rebecca
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Ctr Integrat Genom, Berkeley, CA 94720 USA
关键词
D O I
10.1083/jcb.200610043
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
sThe African clawed frog Xenopus laevis has been instrumental to investigations of both development and cell biology, but the utility of this model organism for genetic and proteomic studies is limited by its long generation time and unsequenced pseudotetraploid genome. Xenopus tropicalis, which is a small, faster-breeding relative of X. laevis, has recently been adopted for research in developmental genetics and functional genomics, and has been chosen for genome sequencing. We show that X. tropicalis egg extracts reconstitute the fundamental cell cycle events of nuclear formation and bipolar spindle assembly around exogenously added sperm nuclei. Interestingly, X. tropicalis spindles were similar to 30% shorter than X. laevis spindles, and mixing experiments revealed a dynamic, dose-dependent regulation of spindle size by cytoplasmic factors. Measurements of microtubule dynamics revealed that microtubules polymerized slower in X. tropicalis extracts compared to X. laevis, but that this difference is unlikely to account for differences in spindle size. Thus, in addition to expanding the range of developmental and cell biological experiments, the use of X. tropicalis provides novel insight into the complex mechanisms that govern spindle morphogenesis.
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收藏
页码:765 / 770
页数:6
相关论文
共 23 条
[1]   XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFβ proteins in Xenopus development [J].
Birsoy, B ;
Berg, L ;
Williams, PH ;
Smith, JC ;
Wylie, CC ;
Christian, JL ;
Heasman, J .
DEVELOPMENT, 2005, 132 (03) :591-602
[2]   A Rae1-containing ribonucleoprotein complex is required for mitotic spindle assembly [J].
Blower, MD ;
Nachury, M ;
Heald, R ;
Weis, K .
CELL, 2005, 121 (02) :223-234
[3]   A tribute to the Xenopus laevis oocyte and egg [J].
Brown, DD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (44) :45291-45299
[4]   Poly(ADP-ribose) is required for spindle assembly and structure [J].
Chang, P ;
Jacobson, MK ;
Mitchison, TJ .
NATURE, 2004, 432 (7017) :645-649
[5]   Reconstruction of the centrosome cycle from cryoelectron micrographs [J].
Chrétien, D ;
Buendia, B ;
Fuller, SD ;
Karsenti, E .
JOURNAL OF STRUCTURAL BIOLOGY, 1997, 120 (02) :117-133
[6]   COMPLETION OF DNA-REPLICATION IS MONITORED BY A FEEDBACK-SYSTEM THAT CONTROLS THE INITIATION OF MITOSIS INVITRO - STUDIES IN XENOPUS [J].
DASSO, M ;
NEWPORT, JW .
CELL, 1990, 61 (05) :811-823
[7]   Anaphase A chromosome movement and poleward spindle microtubule flux occur at similar rates in Xenopus extract spindles [J].
Desai, A ;
Maddox, PS ;
Mitchison, TJ ;
Salmon, ED .
JOURNAL OF CELL BIOLOGY, 1998, 141 (03) :703-713
[8]  
Desai A, 1999, METHOD CELL BIOL, V61, P385
[9]   The Xenopus chromokinesin Xkid is essential for metaphase chromosome alignment and must be degraded to allow anaphase chromosome movement [J].
Funabiki, H ;
Murray, AW .
CELL, 2000, 102 (04) :411-424
[10]   Length control of the metaphase spindle [J].
Goshima, G ;
Wollman, R ;
Stuurman, N ;
Scholey, JM ;
Vale, RD .
CURRENT BIOLOGY, 2005, 15 (22) :1979-1988