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XII. Yeast sequencing reports. Sequence, mapping and disruption of CCC1, a gene that cross‐complements the Ca2+‐sensitive phenotype of csg1 mutants

  • Dadin Fu
  • , Troy Beeler
  • , Teresa Dunn*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

We have isolated, sequenced, mapped and disrupted a novel gene, CCC1, from Saccharomyces cerevisiae. This gene displays non‐allelic complementation of the Ca2+‐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. The sequence has been deposited in the GenBank data library under Accession Number L24112.

Original languageEnglish
Pages (from-to)515-521
Number of pages7
JournalYeast
Volume10
Issue number4
DOIs
StatePublished - Apr 1994

Keywords

  • Ca sensitive mutants
  • calcium regulation
  • CCC1
  • chromosome XII
  • cross‐complementation
  • Saccharomyces cerevisiae

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