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PMID: 9361037 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Efficient conditional mutation of the vertebrate CENP-C gene.

Human molecular genetics ·Vol. 6 ·No. 13 ·1997-12-00 ·Pages 2301-8

Fukagawa T, Brown WR

Abstract

We have used gene targeting in the DT40 cell line to create a cell line which expresses a fusion between CENP-C and a mouse steroid receptor and which behaves as a conditional loss of function mutant of CENP-C. Under restrictive conditions these cells arrest at the metaphase/anaphase junction and after a delay of approximately 2.5 h die by apoptosis. These results indicate that CENP-C is either necessary for anaphase chromosome movement or for mediating a signal which triggers centromere function during anaphase. Our approach is simple and applicable to a wide range of proteins with general cell autonomous functions in vertebrates.

MeSH Terms
Amino Acid Sequence Anaphase/genetics Animals Apoptosis Cell Line Centromere/chemistry,physiology Chickens/genetics Chromosomal Proteins, Non-Histone/genetics,physiology Gene Targeting Humans Mice Molecular Sequence Data Receptors, Drug/drug effects,genetics Recombinant Fusion Proteins/physiology Sequence Alignment Sequence Homology, Amino Acid Tamoxifen/analogs & derivatives,pharmacology Transfection Vertebrates/genetics
Chemicals
Chromosomal Proteins, Non-Histone Receptors, Drug Recombinant Fusion Proteins centromere protein C Tamoxifen afimoxifene
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fukagawa T
Cancer Research Campaign Chromosome Molecular Biology Group, Biochemistry Department, Oxford University, South Parks Road, Oxford OX1 3QU, UK. tfukagaw@bioch.ox.ac.uk
Brown W R
Article Info
Journal
Human molecular genetics
Abbr.
Hum Mol Genet
ISSN
0964-6906
Published
1997-12-00
Pages
2301-8
Language
English
Region
England
NLM ID
9208958
Subset
IM
Databases
GENBANK
AB004649, AB004650
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