Literature DB >> 16987880

Signatures of adaptive evolution within human non-coding sequence.

Chris P Ponting1, Gerton Lunter.   

Abstract

The human genome is often portrayed as consisting of three sequence types, each distinguished by their mode of evolution. Purifying selection is estimated to act on 2.5-5.0% of the genome, whereas virtually all remaining sequence is considered to have evolved neutrally and to be devoid of functionality. The third mode of evolution, positive selection of advantageous changes, is considered rare. Such instances have been inferred only for a handful of sites, and these lie almost exclusively within protein-coding genes. Nevertheless, the majority of positively selected sequence is expected to lie within the wealth of functional 'dark matter' present outside of the coding sequence. Here, we review the evolutionary evidence for the majority of human-conserved DNA lying outside of the protein-coding sequence. We argue that within this non-coding fraction lies at least 1 Mb of functional sequence that has accumulated many beneficial nucleotide replacements. Illuminating the functions of this adaptive dark matter will lead to a better understanding of the sequence changes that have shaped the innovative biology of our species.

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Year:  2006        PMID: 16987880     DOI: 10.1093/hmg/ddl182

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  13 in total

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Review 6.  Human genetics and genomics a decade after the release of the draft sequence of the human genome.

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7.  Organizational heterogeneity of vertebrate genomes.

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8.  Functionality or transcriptional noise? Evidence for selection within long noncoding RNAs.

Authors:  Jasmina Ponjavic; Chris P Ponting; Gerton Lunter
Journal:  Genome Res       Date:  2007-03-26       Impact factor: 9.043

9.  'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health care.

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10.  Catalogues of mammalian long noncoding RNAs: modest conservation and incompleteness.

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Journal:  Genome Biol       Date:  2009-11-06       Impact factor: 13.583

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