Sequence, mapping and disruption of CCC1, a gene that cross-complements the Ca(2+)-sensitive phenotype of csg1 mutants.

Autor: Fu D; Department of Biochemistry, Uniformed Services University of the Health Science, Bethesda, Maryland 20814., Beeler T, Dunn T
Jazyk: angličtina
Zdroj: Yeast (Chichester, England) [Yeast] 1994 Apr; Vol. 10 (4), pp. 515-21.
DOI: 10.1002/yea.320100411
Abstrakt: We have isolated, sequenced, mapped and disrupted a novel gene, CCC1, from Saccharomyces cerevisiae. This gene displays non-allelic complementation of the Ca(2+)-sensitive phenotype conferred by the csg1 mutation. The ability of this gene, in two copies per cell, to reverse the csg1 defect suggests it may have a role in regulating Ca2+ homeostasis. The sequence of CCC1 indicates that it encodes a 322 amino acid, membrane-associated protein. The CCC1 gene is located on the right arm of chromosome XII.
Databáze: MEDLINE