Literature DB >> 2016312

Half-calmodulin is sufficient for cell proliferation. Expressions of N- and C-terminal halves of calmodulin in the yeast Saccharomyces cerevisiae.

G H Sun1, Y Ohya, Y Anraku.   

Abstract

Calmodulin (CaM) has been shown to be an essential component for progression of nuclear division in the yeast Saccharomyces cerevisiae (Ohya, Y., and Anraku, Y. (1989) Curr. Genet. 15, 113-120). To define the functional domain of the molecule required for cell proliferation, we constructed plasmids expressing a series of N- and C-terminal halves of the CaM under the control of the galactose-inducible GAL1 promoter. These plasmids were introduced into a cmd1-disrupted yeast haploid strain, and the growth properties of the cells depending on the half-CaMs were examined. Plasmids expressing the N-terminal half (Ser1-Leu76) and the C-terminal half (Leu85-Cys147), which each maintain two complete EF-hand structures, complemented the growth defect of the cmd1 null mutation, whereas those expressing shorter regions of C- and N-terminal CaM did not. The half-CaMs that complemented the cmd1 null mutation were found to be approximately 6-fold overexpressed relative to expression of native CaM by the wild-type CMD1 gene. The levels of expression of the half CaMs with the true CMD1 promoter were not sufficient for complementation. These results demonstrate that half-CaMs (either the N- or the C-terminal) are capable of supporting growth of yeast cells when they are suitably overproduced. Cells depending solely on half-CaMs all showed a temperature-sensitive growth phenotype, suggesting that half-CaMs cannot carry out all the cellular functions of the complete CaM molecule.

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Year:  1991        PMID: 2016312

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  10 in total

1.  Role of Ca2+ activation and bilobal structure of calmodulin in nuclear and nucleolar localization.

Authors:  Richard Thorogate; Katalin Török
Journal:  Biochem J       Date:  2007-02-15       Impact factor: 3.857

Review 2.  A strange calmodulin of yeast.

Authors:  M Yazawa; K Nakashima; K Yagi
Journal:  Mol Cell Biochem       Date:  1999-01       Impact factor: 3.396

3.  Inhibition of endoplasmic reticulum (ER)-to-Golgi transport induces relocalization of binding protein (BiP) within the ER to form the BiP bodies.

Authors:  S Nishikawa; A Hirata; A Nakano
Journal:  Mol Biol Cell       Date:  1994-10       Impact factor: 4.138

4.  Paramecium Na+ channels activated by Ca(2+)-calmodulin: calmodulin is the Ca2+ sensor in the channel gating mechanism.

Authors:  Y Saimi; K Y Ling
Journal:  J Membr Biol       Date:  1995-04       Impact factor: 1.843

5.  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

6.  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

7.  Calmodulin-dependent protein kinase II and calmodulin are required for induced thermotolerance in Saccharomyces cerevisiae.

Authors:  H Iida; Y Ohya; Y Anraku
Journal:  Curr Genet       Date:  1995-01       Impact factor: 3.886

8.  Immunophilins interact with calcineurin in the absence of exogenous immunosuppressive ligands.

Authors:  M E Cardenas; C Hemenway; R S Muir; R Ye; D Fiorentino; J Heitman
Journal:  EMBO J       Date:  1994-12-15       Impact factor: 11.598

9.  A temperature-sensitive calmodulin mutant loses viability during mitosis.

Authors:  T N Davis
Journal:  J Cell Biol       Date:  1992-08       Impact factor: 10.539

10.  Mutations in yeast calmodulin cause defects in spindle pole body functions and nuclear integrity.

Authors:  G H Sun; A Hirata; Y Ohya; Y Anraku
Journal:  J Cell Biol       Date:  1992-12       Impact factor: 10.539

  10 in total

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