Literature DB >> 15210328

Broad specificity of SR (serine/arginine) proteins in the regulation of alternative splicing of pre-messenger RNA.

Cyril F Bourgeois1, Fabrice Lejeune, James Stévenin.   

Abstract

Alternative splicing of pre-messenger RNA (pre-mRNA) is a highly regulated process that allows expansion of the potential of expression of the genome in higher eukaryotes and involves many factors. Among them, the family of the serine- and arginine-rich proteins (SR proteins) plays a pivotal role: it has essential functions during spliceosome assembly and also interacts with RNA regulatory sequences on the pre-mRNA as well as with multiple cofactors. Collectively, SR proteins, because of their capacity to recognize multiple RNA sequences with a broad specificity, are at the heart of the regulation pathways that lead to the choice of alternative splice sites. Moreover, a growing body of evidence shows that the mechanisms of splicing regulation are not limited to the basic involvement of cis- and trans-acting factors at the pre-mRNA level, but result from intricate pathways, initiated sometimes by stimuli that are external to the cell and integrate SR proteins (and other factors) within an extremely sophisticated network of molecular machines associated with one another. This review focuses on the molecular aspects of the functions of SR proteins. In particular, we discuss the different ways in which SR proteins manage to achieve a high level of specificity in splicing regulation, even though they are also involved in the constitutive reaction.

Mesh:

Substances:

Year:  2004        PMID: 15210328     DOI: 10.1016/S0079-6603(04)78002-2

Source DB:  PubMed          Journal:  Prog Nucleic Acid Res Mol Biol        ISSN: 0079-6603


  83 in total

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Authors:  Kusum K Singh; Steffen Erkelenz; Stephanie Rattay; Anna Katharina Dehof; Andreas Hildebrandt; Klaus Schulze-Osthoff; Heiner Schaal; Christian Schwerk
Journal:  RNA       Date:  2010-10-21       Impact factor: 4.942

3.  A syn-anti conformational difference allows SRSF2 to recognize guanines and cytosines equally well.

Authors:  Gerrit M Daubner; Antoine Cléry; Sandrine Jayne; James Stevenin; Frédéric H-T Allain
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4.  Insights into nuclear organization in plants as revealed by the dynamic distribution of Arabidopsis SR splicing factors.

Authors:  Vinciane Tillemans; Isabelle Leponce; Glwadys Rausin; Laurence Dispa; Patrick Motte
Journal:  Plant Cell       Date:  2006-11-17       Impact factor: 11.277

5.  Molecular anatomy of a speckle.

Authors:  Lisa L Hall; Kelly P Smith; Meg Byron; Jeanne B Lawrence
Journal:  Anat Rec A Discov Mol Cell Evol Biol       Date:  2006-07

6.  Identification of RNA-binding proteins that regulate FGFR2 splicing through the use of sensitive and specific dual color fluorescence minigene assays.

Authors:  Emily A Newman; Stephanie J Muh; Ruben H Hovhannisyan; Claude C Warzecha; Richard B Jones; Wallace L McKeehan; Russ P Carstens
Journal:  RNA       Date:  2006-04-07       Impact factor: 4.942

7.  Looking for organization patterns of highly expressed genes: purine-pyrimidine composition of precursor mRNAs.

Authors:  A Paz; D Mester; E Nevo; A Korol
Journal:  J Mol Evol       Date:  2007-01-08       Impact factor: 2.395

Review 8.  Processive phosphorylation: mechanism and biological importance.

Authors:  Parag Patwardhan; W Todd Miller
Journal:  Cell Signal       Date:  2007-06-22       Impact factor: 4.315

9.  Plant-specific SR-related protein atSR45a interacts with spliceosomal proteins in plant nucleus.

Authors:  Noriaki Tanabe; Ayako Kimura; Kazuya Yoshimura; Shigeru Shigeoka
Journal:  Plant Mol Biol       Date:  2009-02-24       Impact factor: 4.076

10.  DX16 is a novel SR protein phosphorylated by DOA.

Authors:  Yongqi Wan; Mingkuan Sun; Shanzhi Wang; Li Liu; Liudi Yuan; Wei Xie
Journal:  Mol Cell Biochem       Date:  2007-09-09       Impact factor: 3.396

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