Literature DB >> 18753788

Amino acid repeats and the structure and evolution of proteins.

M M Albà1, P Tompa, R A Veitia.   

Abstract

Many proteins have repeats or runs of single amino acids. The pathogenicity of some repeat expansions has fueled proteomic, genomic and structural explorations of homopolymeric runs not only in human but in a wide variety of other organisms. Other types of amino acid repetitive structures exhibit more complex patterns than homopeptides. Irrespective of their precise organization, repetitive sequences are defined as low complexity or simple sequences, as one or a few residues are particularly abundant. Prokaryotes show a relatively low frequency of simple sequences compared to eukaryotes. In the latter the percentage of proteins containing homopolymeric runs varies greatly from one group to another. For instance, within vertebrates, amino acid repeat frequency is much higher in mammals than in amphibians, birds or fishes. For some repeats, this is correlated with the GC-richness of the regions containing the corresponding genes. Homopeptides tend to occur in disordered regions of transcription factors or developmental proteins. They can trigger the formation of protein aggregates, particularly in 'disease' proteins. Simple sequences seem to evolve more rapidly than the rest of the protein/gene and may have a functional impact. Therefore, they are good candidates to promote rapid evolutionary changes. All these diverse facets of homopolymeric runs are explored in this review.

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Year:  2007        PMID: 18753788     DOI: 10.1159/000107607

Source DB:  PubMed          Journal:  Genome Dyn        ISSN: 1660-9263


  15 in total

1.  Expanding the proteome: disordered and alternatively folded proteins.

Authors:  H Jane Dyson
Journal:  Q Rev Biophys       Date:  2011-07-01       Impact factor: 5.318

2.  Genes encoding intrinsic disorder in Eukaryota have high GC content.

Authors:  Zhenling Peng; Vladimir N Uversky; Lukasz Kurgan
Journal:  Intrinsically Disord Proteins       Date:  2016-12-15

Review 3.  Translational Control by Prion-like Proteins.

Authors:  Liying Li; J P McGinnis; Kausik Si
Journal:  Trends Cell Biol       Date:  2018-03-09       Impact factor: 20.808

4.  A fungal transcription factor gene is expressed in plants from its own promoter and improves drought tolerance.

Authors:  Félix Martínez; Anjuman Arif; Sergio G Nebauer; Eduardo Bueso; Rashid Ali; Consuelo Montesinos; Veronique Brunaud; Jesús Muñoz-Bertomeu; Ramón Serrano
Journal:  Planta       Date:  2015-03-26       Impact factor: 4.116

5.  Positive and strongly relaxed purifying selection drive the evolution of repeats in proteins.

Authors:  Erez Persi; Yuri I Wolf; Eugene V Koonin
Journal:  Nat Commun       Date:  2016-11-18       Impact factor: 14.919

6.  Discerning evolutionary trends in post-translational modification and the effect of intrinsic disorder: Analysis of methylation, acetylation and ubiquitination sites in human proteins.

Authors:  Mohanalakshmi Narasumani; Paul M Harrison
Journal:  PLoS Comput Biol       Date:  2018-08-10       Impact factor: 4.475

7.  Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty?

Authors:  Guy Naamati; Menachem Fromer; Michal Linial
Journal:  BMC Genomics       Date:  2009-12-10       Impact factor: 3.969

8.  Dissecting the role of low-complexity regions in the evolution of vertebrate proteins.

Authors:  Núria Radó-Trilla; Mmar Albà
Journal:  BMC Evol Biol       Date:  2012-08-24       Impact factor: 3.260

Review 9.  Regulating highly dynamic unstructured proteins and their coding mRNAs.

Authors:  Buyong Ma; Ruth Nussinov
Journal:  Genome Biol       Date:  2009-01-28       Impact factor: 13.583

10.  Systematic analysis of compositional order of proteins reveals new characteristics of biological functions and a universal correlate of macroevolution.

Authors:  Erez Persi; David Horn
Journal:  PLoS Comput Biol       Date:  2013-11-21       Impact factor: 4.475

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