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Genome-wide screening for cis-regulatory variation using a classical diallel crossing scheme
Large-scale screening studies carried out to date for genetic variants that affect gene regulation are generally limited to descriptions of differences in allele-specific expression (ASE) detected in vivo. Allele-specific differences in gene expression provide evidence for a model whereby cis-acting...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1540733/ https://www.ncbi.nlm.nih.gov/pubmed/16885241 http://dx.doi.org/10.1093/nar/gkl510 |
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author | Kiekens, Raphaël Vercauteren, Annelies Moerkerke, Beatrijs Goetghebeur, Els Van Den Daele, Hilde Sterken, Roel Kuiper, Martin van Eeuwijk, Fred Vuylsteke, Marnik |
author_facet | Kiekens, Raphaël Vercauteren, Annelies Moerkerke, Beatrijs Goetghebeur, Els Van Den Daele, Hilde Sterken, Roel Kuiper, Martin van Eeuwijk, Fred Vuylsteke, Marnik |
author_sort | Kiekens, Raphaël |
collection | PubMed |
description | Large-scale screening studies carried out to date for genetic variants that affect gene regulation are generally limited to descriptions of differences in allele-specific expression (ASE) detected in vivo. Allele-specific differences in gene expression provide evidence for a model whereby cis-acting genetic variation results in differential expression between alleles. Such gene surveys for regulatory variation are a first step in identifying the specific nucleotide changes that govern gene expression differences, but they leave the underlying mechanisms unexplored. Here, we propose a quantitative genetics approach to perform a genome-wide analysis of ASE differences (GASED). The GASED approach is based on a diallel design that is often used in plant breeding programs to estimate general combining abilities (GCA) of specific inbred lines and to identify high-yielding hybrid combinations of parents based on their specific combining abilities (SCAs). In a context of gene expression, the values of GCA and SCA parameters allow cis- and trans-regulatory changes to be distinguished and imbalances in gene expression to be ascribed to cis-regulatory variation. With this approach, a total of 715 genes could be identified that are likely to carry allelic polymorphisms responsible for at least a 1.5-fold allelic expression difference in a total of 10 diploid Arabidopsis thaliana hybrids. The major strength of the GASED approach, compared to other ASE detection methods, is that it is not restricted to genes with allelic transcript variants. Although a false-positive rate of 9/41 was observed, the GASED approach is a valuable pre-screening method that can accelerate systematic surveys of naturally occurring cis-regulatory variation among inbred lines for laboratory species, such as Arabidopsis, mouse, rat and fruitfly, and economically important crop species, such as corn. |
format | Text |
id | pubmed-1540733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-15407332006-08-24 Genome-wide screening for cis-regulatory variation using a classical diallel crossing scheme Kiekens, Raphaël Vercauteren, Annelies Moerkerke, Beatrijs Goetghebeur, Els Van Den Daele, Hilde Sterken, Roel Kuiper, Martin van Eeuwijk, Fred Vuylsteke, Marnik Nucleic Acids Res Article Large-scale screening studies carried out to date for genetic variants that affect gene regulation are generally limited to descriptions of differences in allele-specific expression (ASE) detected in vivo. Allele-specific differences in gene expression provide evidence for a model whereby cis-acting genetic variation results in differential expression between alleles. Such gene surveys for regulatory variation are a first step in identifying the specific nucleotide changes that govern gene expression differences, but they leave the underlying mechanisms unexplored. Here, we propose a quantitative genetics approach to perform a genome-wide analysis of ASE differences (GASED). The GASED approach is based on a diallel design that is often used in plant breeding programs to estimate general combining abilities (GCA) of specific inbred lines and to identify high-yielding hybrid combinations of parents based on their specific combining abilities (SCAs). In a context of gene expression, the values of GCA and SCA parameters allow cis- and trans-regulatory changes to be distinguished and imbalances in gene expression to be ascribed to cis-regulatory variation. With this approach, a total of 715 genes could be identified that are likely to carry allelic polymorphisms responsible for at least a 1.5-fold allelic expression difference in a total of 10 diploid Arabidopsis thaliana hybrids. The major strength of the GASED approach, compared to other ASE detection methods, is that it is not restricted to genes with allelic transcript variants. Although a false-positive rate of 9/41 was observed, the GASED approach is a valuable pre-screening method that can accelerate systematic surveys of naturally occurring cis-regulatory variation among inbred lines for laboratory species, such as Arabidopsis, mouse, rat and fruitfly, and economically important crop species, such as corn. Oxford University Press 2006 2006-08-02 /pmc/articles/PMC1540733/ /pubmed/16885241 http://dx.doi.org/10.1093/nar/gkl510 Text en © 2006 The Author(s) |
spellingShingle | Article Kiekens, Raphaël Vercauteren, Annelies Moerkerke, Beatrijs Goetghebeur, Els Van Den Daele, Hilde Sterken, Roel Kuiper, Martin van Eeuwijk, Fred Vuylsteke, Marnik Genome-wide screening for cis-regulatory variation using a classical diallel crossing scheme |
title | Genome-wide screening for cis-regulatory variation using a classical diallel crossing scheme |
title_full | Genome-wide screening for cis-regulatory variation using a classical diallel crossing scheme |
title_fullStr | Genome-wide screening for cis-regulatory variation using a classical diallel crossing scheme |
title_full_unstemmed | Genome-wide screening for cis-regulatory variation using a classical diallel crossing scheme |
title_short | Genome-wide screening for cis-regulatory variation using a classical diallel crossing scheme |
title_sort | genome-wide screening for cis-regulatory variation using a classical diallel crossing scheme |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1540733/ https://www.ncbi.nlm.nih.gov/pubmed/16885241 http://dx.doi.org/10.1093/nar/gkl510 |
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