Literature DB >> 26032716

Evolution of new functions de novo and from preexisting genes.

Dan I Andersson1, Jon Jerlström-Hultqvist1, Joakim Näsvall1.   

Abstract

How the enormous structural and functional diversity of new genes and proteins was generated (estimated to be 10(10)-10(12) different proteins in all organisms on earth [Choi I-G, Kim S-H. 2006. Evolution of protein structural classes and protein sequence families. Proc Natl Acad Sci 103: 14056-14061] is a central biological question that has a long and rich history. Extensive work during the last 80 years have shown that new genes that play important roles in lineage-specific phenotypes and adaptation can originate through a multitude of different mechanisms, including duplication, lateral gene transfer, gene fusion/fission, and de novo origination. In this review, we focus on two main processes as generators of new functions: evolution of new genes by duplication and divergence of pre-existing genes and de novo gene origination in which a whole protein-coding gene evolves from a noncoding sequence.
Copyright © 2015 Cold Spring Harbor Laboratory Press; all rights reserved.

Mesh:

Year:  2015        PMID: 26032716      PMCID: PMC4448608          DOI: 10.1101/cshperspect.a017996

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Biol        ISSN: 1943-0264            Impact factor:   10.005


  100 in total

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4.  Rapid expansion and functional divergence of subtelomeric gene families in yeasts.

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5.  Recent de novo origin of human protein-coding genes.

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10.  Amplification-mutagenesis: evidence that "directed" adaptive mutation and general hypermutability result from growth with a selected gene amplification.

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Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-05       Impact factor: 11.205

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  38 in total

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Journal:  Structure       Date:  2017-10-12       Impact factor: 5.006

Review 8.  The Role of Sequence Duplication in Transcriptional Regulation and Genome Evolution.

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Review 9.  All For One and One For All on the Tick-Host Battlefield.

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10.  The YsrS Paralog DygS Has the Capacity To Activate Expression of the Yersinia enterocolitica Ysa Type III Secretion System.

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Journal:  J Bacteriol       Date:  2016-05-27       Impact factor: 3.490

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