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Mixture modeling of transcript abundance classes in natural populations

BACKGROUND: Populations diverge in genotype and phenotype under the influence of such evolutionary processes as genetic drift, mutation accumulation, and natural selection. Because genotype maps onto phenotype by way of transcription, it is of interest to evaluate how these evolutionary factors infl...

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Autores principales: Hsieh, Wen-Ping, Passador-Gurgel, Gisele, Stone, Eric A, Gibson, Greg
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394757/
https://www.ncbi.nlm.nih.gov/pubmed/17547747
http://dx.doi.org/10.1186/gb-2007-8-6-r98
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author Hsieh, Wen-Ping
Passador-Gurgel, Gisele
Stone, Eric A
Gibson, Greg
author_facet Hsieh, Wen-Ping
Passador-Gurgel, Gisele
Stone, Eric A
Gibson, Greg
author_sort Hsieh, Wen-Ping
collection PubMed
description BACKGROUND: Populations diverge in genotype and phenotype under the influence of such evolutionary processes as genetic drift, mutation accumulation, and natural selection. Because genotype maps onto phenotype by way of transcription, it is of interest to evaluate how these evolutionary factors influence the structure of variation at the level of transcription. Here, we explore the distributions of cis-acting and trans-acting factors and their relative contributions to expression of transcripts that exhibit two or more classes of abundance among individuals within populations. RESULTS: Expression profiling using cDNA microarrays was conducted in Drosophila melanogaster adult female heads for 58 nearly isogenic lines from a North Carolina population and 50 from a California population. Using a mixture modeling approach, transcripts were identified that exhibit more than one mode of transcript abundance across the samples. Power studies indicate that sample sizes of 50 individuals will generally be sufficient to detect divergent transcript abundance classes. The distribution of transcript abundance classes is skewed toward low frequency minor classes, which is reminiscent of the typical skew in genotype frequencies. Similar results are observed in reported data on gene expression in human lymphoblast cell lines, in which analysis of association with linked polymorphisms implies that cis-acting single nucleotide polymorphisms make only a modest contribution to bimodal distributions of transcript abundance. CONCLUSION: Population surveys of gene expression may complement genetical genomics as a general approach to quantifying sources of transcriptional variation. Differential expression of transcripts among individuals is due to a complex interplay of cis-acting and trans-acting factors.
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spelling pubmed-23947572008-05-29 Mixture modeling of transcript abundance classes in natural populations Hsieh, Wen-Ping Passador-Gurgel, Gisele Stone, Eric A Gibson, Greg Genome Biol Research BACKGROUND: Populations diverge in genotype and phenotype under the influence of such evolutionary processes as genetic drift, mutation accumulation, and natural selection. Because genotype maps onto phenotype by way of transcription, it is of interest to evaluate how these evolutionary factors influence the structure of variation at the level of transcription. Here, we explore the distributions of cis-acting and trans-acting factors and their relative contributions to expression of transcripts that exhibit two or more classes of abundance among individuals within populations. RESULTS: Expression profiling using cDNA microarrays was conducted in Drosophila melanogaster adult female heads for 58 nearly isogenic lines from a North Carolina population and 50 from a California population. Using a mixture modeling approach, transcripts were identified that exhibit more than one mode of transcript abundance across the samples. Power studies indicate that sample sizes of 50 individuals will generally be sufficient to detect divergent transcript abundance classes. The distribution of transcript abundance classes is skewed toward low frequency minor classes, which is reminiscent of the typical skew in genotype frequencies. Similar results are observed in reported data on gene expression in human lymphoblast cell lines, in which analysis of association with linked polymorphisms implies that cis-acting single nucleotide polymorphisms make only a modest contribution to bimodal distributions of transcript abundance. CONCLUSION: Population surveys of gene expression may complement genetical genomics as a general approach to quantifying sources of transcriptional variation. Differential expression of transcripts among individuals is due to a complex interplay of cis-acting and trans-acting factors. BioMed Central 2007 2007-06-04 /pmc/articles/PMC2394757/ /pubmed/17547747 http://dx.doi.org/10.1186/gb-2007-8-6-r98 Text en Copyright © 2007 Hsieh et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Hsieh, Wen-Ping
Passador-Gurgel, Gisele
Stone, Eric A
Gibson, Greg
Mixture modeling of transcript abundance classes in natural populations
title Mixture modeling of transcript abundance classes in natural populations
title_full Mixture modeling of transcript abundance classes in natural populations
title_fullStr Mixture modeling of transcript abundance classes in natural populations
title_full_unstemmed Mixture modeling of transcript abundance classes in natural populations
title_short Mixture modeling of transcript abundance classes in natural populations
title_sort mixture modeling of transcript abundance classes in natural populations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394757/
https://www.ncbi.nlm.nih.gov/pubmed/17547747
http://dx.doi.org/10.1186/gb-2007-8-6-r98
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