Literature DB >> 10970765

The calmodulin multigene family as a unique case of genetic redundancy: multiple levels of regulation to provide spatial and temporal control of calmodulin pools?

S L Toutenhoofd1, E E Strehler.   

Abstract

Calmodulin (CaM) is a ubiquitous, highly conserved calcium sensor protein involved in the regulation of a wide variety of cellular events. In vertebrates, an identical CaM protein is encoded by a family of non-allelic genes, raising questions concerning the evolutionary pressure responsible for the maintenance of this apparently redundant family. Here we review the evidence that the control of the spatial and temporal availability of CaM may require multiple regulatory levels to ensure the proper localization, maintenance and size of intracellular CaM pools. Differential transcription of the CaM genes provides one level of regulation to meet tissue-specific, developmental and cell-specific needs for altered CaM levels. Post-transcriptional regulation occurs at the level of mRNA stability, perhaps dependent on alternative polyadenylation and differences in the untranslated sequences of the multiple gene transcripts. Recent evidence indicates that trafficking of specific CaM mRNAs may occur to specialized cellular locales such as the dendrites of neurons. This could allow local CaM synthesis and thereby help generate local pools of CaM. Local CaM activity may be further regulated by post-translational mechanisms such as phosphorylation or storage of CaM in a 'masked' form. The spatial resolution of CaM activity is enhanced by the limited free diffusion of CaM combined with differential affinity for and availability of target proteins. Preserving multiple CaM genes with divergent noncoding sequences may be necessary in complex organisms to ensure that the many CaM-dependent processes occur with the requisite spatial and temporal resolution. Transgenic mouse models and studies on mice carrying single and double gene 'knockouts' promise to shed further light on the role of specificity versus redundancy in the evolutionary maintenance of the vertebrate CaM multigene family.

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Year:  2000        PMID: 10970765     DOI: 10.1054/ceca.2000.0136

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


  28 in total

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Journal:  Mol Biol Cell       Date:  2003-03       Impact factor: 4.138

2.  Calmodulins and related potential calcium sensors of Arabidopsis.

Authors:  Elizabeth McCormack; Janet Braam
Journal:  New Phytol       Date:  2003-09       Impact factor: 10.151

3.  Emanuel Strehler's work on calcium pumps and calcium signaling.

Authors:  Emanuel E Strehler
Journal:  World J Biol Chem       Date:  2011-04-26

Review 4.  Gap junction regulation by calmodulin.

Authors:  Juan Zou; Mani Salarian; Yanyi Chen; Richard Veenstra; Charles F Louis; Jenny J Yang
Journal:  FEBS Lett       Date:  2014-01-16       Impact factor: 4.124

5.  The Calmodulin-Binding Protein IQM1 Interacts with CATALASE2 to Affect Pathogen Defense.

Authors:  Tianxiao Lv; Xiaoming Li; Tian Fan; Huiting Luo; Chuping Xie; Yuping Zhou; Chang-En Tian
Journal:  Plant Physiol       Date:  2019-09-23       Impact factor: 8.340

6.  MicroRNA-1 negatively regulates expression of the hypertrophy-associated calmodulin and Mef2a genes.

Authors:  Sadakatsu Ikeda; Aibin He; Sek Won Kong; Jun Lu; Rafael Bejar; Natalya Bodyak; Kyu-Ho Lee; Qing Ma; Peter M Kang; Todd R Golub; William T Pu
Journal:  Mol Cell Biol       Date:  2009-02-02       Impact factor: 4.272

7.  Protein kinase Cdelta and calmodulin regulate epidermal growth factor receptor recycling from early endosomes through Arp2/3 complex and cortactin.

Authors:  Anna Lladó; Paul Timpson; Sandra Vilà de Muga; Jemina Moretó; Albert Pol; Thomas Grewal; Roger J Daly; Carlos Enrich; Francesc Tebar
Journal:  Mol Biol Cell       Date:  2007-10-24       Impact factor: 4.138

8.  Calmodulin modulates Akt activity in human breast cancer cell lines.

Authors:  Christine M Coticchia; Chetana M Revankar; Tushar B Deb; Robert B Dickson; Michael D Johnson
Journal:  Breast Cancer Res Treat       Date:  2008-06-28       Impact factor: 4.872

9.  Presence of activating KRAS mutations correlates significantly with expression of tumour suppressor genes DCN and TPM1 in colorectal cancer.

Authors:  Vid Mlakar; Gasper Berginc; Metka Volavsek; Zdravko Stor; Miran Rems; Damjan Glavac
Journal:  BMC Cancer       Date:  2009-08-13       Impact factor: 4.430

10.  Neurogranin enhances synaptic strength through its interaction with calmodulin.

Authors:  Ling Zhong; Tiffani Cherry; Christine E Bies; Matthew A Florence; Nashaat Z Gerges
Journal:  EMBO J       Date:  2009-08-27       Impact factor: 11.598

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