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Evidence for turnover of functional noncoding DNA in mammalian genome evolution.

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Evidence for turnover of functional noncoding DNA in mammalian genome evolution. / Smith, Nick G.C.; Brandström, Mikael; Ellegren, Hans.
In: Genomics, Vol. 84, No. 5, 11.2004, p. 806-813.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Smith, NGC, Brandström, M & Ellegren, H 2004, 'Evidence for turnover of functional noncoding DNA in mammalian genome evolution.', Genomics, vol. 84, no. 5, pp. 806-813. https://doi.org/10.1016/j.ygeno.2004.07.012

APA

Smith, N. G. C., Brandström, M., & Ellegren, H. (2004). Evidence for turnover of functional noncoding DNA in mammalian genome evolution. Genomics, 84(5), 806-813. https://doi.org/10.1016/j.ygeno.2004.07.012

Vancouver

Smith NGC, Brandström M, Ellegren H. Evidence for turnover of functional noncoding DNA in mammalian genome evolution. Genomics. 2004 Nov;84(5):806-813. doi: 10.1016/j.ygeno.2004.07.012

Author

Smith, Nick G.C. ; Brandström, Mikael ; Ellegren, Hans. / Evidence for turnover of functional noncoding DNA in mammalian genome evolution. In: Genomics. 2004 ; Vol. 84, No. 5. pp. 806-813.

Bibtex

@article{06eafbc51d0645d99cf9c6d073b1edd5,
title = "Evidence for turnover of functional noncoding DNA in mammalian genome evolution.",
abstract = "The vast majority of the mammalian genome does not code for proteins, and a fundamental question in genomics is: What proportion of the noncoding mammalian genome is functional? Most attempts to address this issue use sequence comparisons between highly diverged mammals such as human and mouse to identify conservation due to negative selection. But such comparisons will underestimate the true proportion of functional noncoding DNA if there is turnover, if patterns of negative selection change over time. Here we test whether the inferred level of negative selection differs between different pairwise species comparisons. Using a multiple alignment of more than a megabase of contiguous sequence from eight mammalian species, we find a strong negative relationship between inferred levels of negative selection and pairwise divergence using 21 pairwise comparisons. This result suggests that there is a high rate of turnover of functional noncoding elements in the mammalian genome, so measures of functional constraint based on human–mouse comparisons may seriously underestimate the true value.",
author = "Smith, {Nick G.C.} and Mikael Brandstr{\"o}m and Hans Ellegren",
year = "2004",
month = nov,
doi = "10.1016/j.ygeno.2004.07.012",
language = "English",
volume = "84",
pages = "806--813",
journal = "Genomics",
publisher = "Academic Press Inc.",
number = "5",

}

RIS

TY - JOUR

T1 - Evidence for turnover of functional noncoding DNA in mammalian genome evolution.

AU - Smith, Nick G.C.

AU - Brandström, Mikael

AU - Ellegren, Hans

PY - 2004/11

Y1 - 2004/11

N2 - The vast majority of the mammalian genome does not code for proteins, and a fundamental question in genomics is: What proportion of the noncoding mammalian genome is functional? Most attempts to address this issue use sequence comparisons between highly diverged mammals such as human and mouse to identify conservation due to negative selection. But such comparisons will underestimate the true proportion of functional noncoding DNA if there is turnover, if patterns of negative selection change over time. Here we test whether the inferred level of negative selection differs between different pairwise species comparisons. Using a multiple alignment of more than a megabase of contiguous sequence from eight mammalian species, we find a strong negative relationship between inferred levels of negative selection and pairwise divergence using 21 pairwise comparisons. This result suggests that there is a high rate of turnover of functional noncoding elements in the mammalian genome, so measures of functional constraint based on human–mouse comparisons may seriously underestimate the true value.

AB - The vast majority of the mammalian genome does not code for proteins, and a fundamental question in genomics is: What proportion of the noncoding mammalian genome is functional? Most attempts to address this issue use sequence comparisons between highly diverged mammals such as human and mouse to identify conservation due to negative selection. But such comparisons will underestimate the true proportion of functional noncoding DNA if there is turnover, if patterns of negative selection change over time. Here we test whether the inferred level of negative selection differs between different pairwise species comparisons. Using a multiple alignment of more than a megabase of contiguous sequence from eight mammalian species, we find a strong negative relationship between inferred levels of negative selection and pairwise divergence using 21 pairwise comparisons. This result suggests that there is a high rate of turnover of functional noncoding elements in the mammalian genome, so measures of functional constraint based on human–mouse comparisons may seriously underestimate the true value.

U2 - 10.1016/j.ygeno.2004.07.012

DO - 10.1016/j.ygeno.2004.07.012

M3 - Journal article

VL - 84

SP - 806

EP - 813

JO - Genomics

JF - Genomics

IS - 5

ER -