Literature DB >> 12938174

Intrinsically unstructured proteins evolve by repeat expansion.

Peter Tompa1.   

Abstract

The proportion of the genome encoding intrinsically unstructured proteins increases with the complexity of organisms, which demands specific mechanism(s) for generating novel genetic material of this sort. Here it is suggested that one such mechanism is the expansion of internal repeat regions, i.e., coding micro- and minisatellites. An analysis of 126 known unstructured sequences shows the preponderance of repeats: the percentage of proteins with tandemly repeated short segments is much higher in this class (39%) than earlier reported for all Swiss-Prot (14%), yeast (18%) or human (28%) proteins. Furthermore, prime examples, such as salivary proline-rich proteins, titin, eukaryotic RNA polymerase II, the prion protein and several others, demonstrate that the repetitive segments carry fundamental function in these proteins. In addition, their repeat numbers show functionally significant interspecies variation and polymorphism, which underlines that these regions have been shaped by intense evolutionary activity. In all, the major point of this paper is that the genetic instability of repetitive regions combined with the structurally and functionally permissive nature of unstructured proteins has powered the extension and possible functional expansion of this newly recognized protein class. Copyright 2003 Wiley Periodicals, Inc.

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Year:  2003        PMID: 12938174     DOI: 10.1002/bies.10324

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  97 in total

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Authors:  Justin Yamada; Joshua L Phillips; Samir Patel; Gabriel Goldfien; Alison Calestagne-Morelli; Hans Huang; Ryan Reza; Justin Acheson; Viswanathan V Krishnan; Shawn Newsam; Ajay Gopinathan; Edmond Y Lau; Michael E Colvin; Vladimir N Uversky; Michael F Rexach
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Authors:  Loris Mularoni; Alice Ledda; Macarena Toll-Riera; M Mar Albà
Journal:  Genome Res       Date:  2010-03-24       Impact factor: 9.043

3.  Harnessing disorder: onychophorans use highly unstructured proteins, not silks, for prey capture.

Authors:  Victoria S Haritos; Ajay Niranjane; Sarah Weisman; Holly E Trueman; Alagacone Sriskantha; Tara D Sutherland
Journal:  Proc Biol Sci       Date:  2010-06-02       Impact factor: 5.349

4.  Proline-rich salivary proteins have extended conformations.

Authors:  Hélène Boze; Thérèse Marlin; Dominique Durand; Javier Pérez; Aude Vernhet; Francis Canon; Pascale Sarni-Manchado; Véronique Cheynier; Bernard Cabane
Journal:  Biophys J       Date:  2010-07-21       Impact factor: 4.033

5.  Rational design of p53, an intrinsically unstructured protein, for the fabrication of novel molecular sensors.

Authors:  Melissa L Geddie; Taryn L O'Loughlin; Kristen K Woods; Ichiro Matsumura
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Review 6.  The origins of polypeptide domains.

Authors:  Edward E Schmidt; Christopher J Davies
Journal:  Bioessays       Date:  2007-03       Impact factor: 4.345

7.  Dynamic behavior of an intrinsically unstructured linker domain is conserved in the face of negligible amino acid sequence conservation.

Authors:  Gary W Daughdrill; Pranesh Narayanaswami; Sara H Gilmore; Agniezka Belczyk; Celeste J Brown
Journal:  J Mol Evol       Date:  2007-08-25       Impact factor: 2.395

8.  Crosstalk between phosphorylation and multi-site arginine/lysine methylation in C/EBPs.

Authors:  Achim Leutz; Ole Pless; Michael Lappe; Gunnar Dittmar; Elisabeth Kowenz-Leutz
Journal:  Transcription       Date:  2011 Jan-Feb

9.  Intrinsic disorder in protein interactions: insights from a comprehensive structural analysis.

Authors:  Jessica H Fong; Benjamin A Shoemaker; Sergiy O Garbuzynskiy; Michail Y Lobanov; Oxana V Galzitskaya; Anna R Panchenko
Journal:  PLoS Comput Biol       Date:  2009-03-13       Impact factor: 4.475

10.  Tandem and cryptic amino acid repeats accumulate in disordered regions of proteins.

Authors:  Michelle Simon; John M Hancock
Journal:  Genome Biol       Date:  2009-06-01       Impact factor: 13.583

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