Literature DB >> 3180244

In vitro reactivation of anaphase B in isolated spindles of the sea urchin egg.

L I Rebhun1, R E Palazzo.   

Abstract

Spindles may be isolated from sea urchin eggs so that some mitotic processes can be reactivated in vitro. The isolation media allow spindles to remain stable for days. Transfer of the spindles to reactivation media results in loss of birefringence and breakdown of the matrix within which the microtubules function. If, however, tubulin and either guanosine triphosphate or adenosine triphosphate are present in these media so that tubulin can cycle, the spindles do not break down but grow in size and birefringence and show some of the movements of in vivo spindles. The most prominent is that of anaphase B if the mitotic apparatuses (MAs) have been isolated at a time when anaphase was initiated. When isolated during metaphase, MAs either do not show chromosome movement or, if they do, it is a random movement which causes redistribution of the chromosomes on the spindle surface. In either case, such metaphase spindles grow in size and birefringence. Thus under the proper conditions, cycling microtubules can interact with the spindle matrix to induce chromosome movements which resemble those seen in in vivo cells in the case of anaphase B and show some aspects of anaphase A in at least half the spindles isolated at metaphase, although such movements are not coordinated to show a true anaphase movement.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3180244     DOI: 10.1002/cm.970100124

Source DB:  PubMed          Journal:  Cell Motil Cytoskeleton        ISSN: 0886-1544


  9 in total

Review 1.  Do nuclear envelope and intranuclear proteins reorganize during mitosis to form an elastic, hydrogel-like spindle matrix?

Authors:  Kristen M Johansen; Arthur Forer; Changfu Yao; Jack Girton; Jørgen Johansen
Journal:  Chromosome Res       Date:  2011-04       Impact factor: 5.239

2.  In vitro reactivation of spindle elongation in fission yeast nuc2 mutant cells.

Authors:  H Masuda; T Hirano; M Yanagida; W Z Cande
Journal:  J Cell Biol       Date:  1990-02       Impact factor: 10.539

3.  NuMA is required for the organization of microtubules into aster-like mitotic arrays.

Authors:  T Gaglio; A Saredi; D A Compton
Journal:  J Cell Biol       Date:  1995-11       Impact factor: 10.539

4.  Chromosome movement in mitosis requires microtubule anchorage at spindle poles.

Authors:  M B Gordon; L Howard; D A Compton
Journal:  J Cell Biol       Date:  2001-02-05       Impact factor: 10.539

5.  Polyribosome targeting to microtubules: enrichment of specific mRNAs in a reconstituted microtubule preparation from sea urchin embryos.

Authors:  D Hamill; J Davis; J Drawbridge; K A Suprenant
Journal:  J Cell Biol       Date:  1994-11       Impact factor: 10.539

6.  Roles of kinesin and kinesin-like proteins in sea urchin embryonic cell division: evaluation using antibody microinjection.

Authors:  B D Wright; M Terasaki; J M Scholey
Journal:  J Cell Biol       Date:  1993-11       Impact factor: 10.539

7.  DSK1, a novel kinesin-related protein from the diatom Cylindrotheca fusiformis that is involved in anaphase spindle elongation.

Authors:  H Wein; M Foss; B Brady; W Z Cande
Journal:  J Cell Biol       Date:  1996-05       Impact factor: 10.539

Review 8.  A Brief History of Research on Mitotic Mechanisms.

Authors:  J Richard McIntosh; Thomas Hays
Journal:  Biology (Basel)       Date:  2016-12-21

9.  Physiological evidence for involvement of a kinesin-related protein during anaphase spindle elongation in diatom central spindles.

Authors:  C J Hogan; L Stephens; T Shimizu; W Z Cande
Journal:  J Cell Biol       Date:  1992-12       Impact factor: 10.539

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.