Literature DB >> 1505005

Mutational analysis of calmodulin in Saccharomyces cerevisiae.

T N Davis1.   

Abstract

Calmodulin is well characterized as an intracellular Ca2+ receptor in nonproliferating tissues such as muscle and brain. Several observations indicate that calmodulin is also required for cellular growth and division. Deletion of the calmodulin gene is a lethal mutation in Saccharomyces cerevisiae, Schizosaccharomyces pombe and Aspergillus nidulans. Expression of calmodulin antisense RNA in mouse C127 cells causes a transient arrest at G1 and metaphase. Although these results indicate calmodulin plays a critical function during proliferation, they do not reveal the function. S. cerevisiae offers an excellent system for identifying calmodulin functions. Because calmodulin mutants can be readily constructed by gene replacement the consequences of mutations in calmodulin can be directly examined in vivo without interference from wild-type calmodulin. The available wealth of information concerning all aspects of the yeast life cycle provides a large framework for interpretation of new results. The recent dissection of cell cycle regulation is just the latest example of the important insights provided by analyzing basic cellular processes in yeast. Whether studies of calmodulin in yeast will reveal a universal function is unknown. One encouraging result is that yeast cells relying on vertebrate calmodulin as their only source of calmodulin survive and grow well, even if the amount of vertebrate calmodulin is equivalent to the normal steady state levels of yeast calmodulin. This review discusses the varied techniques we are using to identify the functions of calmodulin in yeast. As part of the analysis, we are defining the essential elements of calmodulin structure.

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Year:  1992        PMID: 1505005     DOI: 10.1016/0143-4160(92)90056-x

Source DB:  PubMed          Journal:  Cell Calcium        ISSN: 0143-4160            Impact factor:   6.817


  8 in total

1.  Coupling unbiased mutagenesis to high-throughput DNA sequencing uncovers functional domains in the Ndc80 kinetochore protein of Saccharomyces cerevisiae.

Authors:  Jerry F Tien; Kimberly K Fong; Neil T Umbreit; Celia Payen; Alex Zelter; Charles L Asbury; Maitreya J Dunham; Trisha N Davis
Journal:  Genetics       Date:  2013-07-05       Impact factor: 4.562

2.  Calmodulin point mutations affect Drosophila development and behavior.

Authors:  H B Nelson; R G Heiman; C Bolduc; G E Kovalick; P Whitley; M Stern; K Beckingham
Journal:  Genetics       Date:  1997-12       Impact factor: 4.562

3.  Analysis of a spindle pole body mutant reveals a defect in biorientation and illuminates spindle forces.

Authors:  Tennessee J Yoder; Mark A McElwain; Susan E Francis; Joy Bagley; Eric G D Muller; Brian Pak; Eileen T O'Toole; Mark Winey; Trisha N Davis
Journal:  Mol Biol Cell       Date:  2004-11-03       Impact factor: 4.138

4.  A glutathione reductase mutant of yeast accumulates high levels of oxidized glutathione and requires thioredoxin for growth.

Authors:  E G Muller
Journal:  Mol Biol Cell       Date:  1996-11       Impact factor: 4.138

5.  Gain-of-function mutations in a human calmodulin-like protein identify residues critical for calmodulin action in yeast.

Authors:  E Harris; P Yaswen; J Thorner
Journal:  Mol Gen Genet       Date:  1995-04-20

6.  Structure-based systematic isolation of conditional-lethal mutations in the single yeast calmodulin gene.

Authors:  Y Ohya; D Botstein
Journal:  Genetics       Date:  1994-12       Impact factor: 4.562

7.  The Ndc80 complex bridges two Dam1 complex rings.

Authors:  Jae Ook Kim; Alex Zelter; Neil T Umbreit; Athena Bollozos; Michael Riffle; Richard Johnson; Michael J MacCoss; Charles L Asbury; Trisha N Davis
Journal:  Elife       Date:  2017-02-13       Impact factor: 8.140

8.  The yeast centrin, cdc31p, and the interacting protein kinase, Kic1p, are required for cell integrity.

Authors:  D S Sullivan; S Biggins; M D Rose
Journal:  J Cell Biol       Date:  1998-11-02       Impact factor: 10.539

  8 in total

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