Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1994 Dec;127(6 Pt 1):1655-70.
doi: 10.1083/jcb.127.6.1655.

Bypassing anaphase by fission yeast cut9 mutation: requirement of cut9+ to initiate anaphase

Affiliations
Comparative Study

Bypassing anaphase by fission yeast cut9 mutation: requirement of cut9+ to initiate anaphase

I Samejima et al. J Cell Biol. 1994 Dec.

Abstract

A novel anaphase block phenotype was found in fission yeast temperature-sensitive cut9 mutants. Cells enter mitosis with chromosome condensation and short spindle formation, then block anaphase, but continue to progress into postanaphase events such as degradation of the spindle, reformation of the postanaphase cytoplasmic microtubule arrays, septation, and cytokinesis. The cut9 mutants are defective in the onset of anaphase and possibly in the restraint of postanaphase events until the completion of anaphase. The cut9+ gene encodes a 78-kD protein containing the 10 34-amino acid repeats, tetratricopeptide repeats (TPR), and similar to budding yeast Cdc16. It is essential for viability, and the mutation sites reside in the TPR. The three genes, namely, nuc2+, scn1+, and scn2+, genetically interact with cut9+. The nuc2+ and cut9+ genes share an essential function to initiate anaphase. The cold-sensitive scn1 and scn2 mutations, defective in late anaphase, can suppress the ts phenotype of cut9.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Bioessays. 1993 Dec;15(12):775-82 - PubMed
    1. Cell. 1990 Sep 7;62(5):913-25 - PubMed
    1. Trends Biochem Sci. 1991 May;16(5):173-7 - PubMed
    1. Cell. 1993 Jul 2;73(7):1393-402 - PubMed
    1. Nature. 1992 Oct 15;359(6396):599-604 - PubMed

Publication types

MeSH terms

Substances

Associated data