Gene evolutionary trajectories and GC patterns driven by recombination in Zea mays

Recombination occurring during meiosis is critical for creating genetic variation and plays an essential role in plant evolution. In addition to creating novel gene combinations, recombination can affect genome structure through altering GC patterns. In maize (Zea mays) and other grasses, another in...

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Main Authors: Anitha Sundararajan, Stefanie Dukowic-Schulze, Madeline Kwicklis, Kayla Engstrom, Nathan Garcia, Oliver J Oviedo, Thiruvarangan Ramaraj, Michael D Gonzales, Yan He, Minghui Wang, Qi Sun, Jaroslaw Pillardy, Shahryar F Kianian, Wojciech P Pawlowski, Changbin Chen, Joann Mudge
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-09-01
Series:Frontiers in Plant Science
Subjects:
GC
Online Access:http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01433/full
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spelling doaj-c95da4924f7b4a738fb874a93079817b2020-11-24T21:28:14ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2016-09-01710.3389/fpls.2016.01433220732Gene evolutionary trajectories and GC patterns driven by recombination in Zea maysAnitha Sundararajan0Stefanie Dukowic-Schulze1Madeline Kwicklis2Kayla Engstrom3Nathan Garcia4Oliver J Oviedo5Thiruvarangan Ramaraj6Michael D Gonzales7Yan He8Minghui Wang9Minghui Wang10Qi Sun11Jaroslaw Pillardy12Shahryar F Kianian13Wojciech P Pawlowski14Changbin Chen15Joann Mudge16National Center for Genome ResourcesUniversity of MinnesotaNational Center for Genome ResourcesNational Center for Genome ResourcesNational Center for Genome ResourcesNational Center for Genome ResourcesNational Center for Genome ResourcesNational Center for Genome ResourcesCornell UniversityCornell UniversityCornell UniversityCornell UniversityCornell UniversityUSDA-ARSCornell UniversityUniversity of MinnesotaNational Center for Genome ResourcesRecombination occurring during meiosis is critical for creating genetic variation and plays an essential role in plant evolution. In addition to creating novel gene combinations, recombination can affect genome structure through altering GC patterns. In maize (Zea mays) and other grasses, another intriguing GC pattern exists. Maize genes show a bimodal GC content distribution that has been attributed to nucleotide bias in the third, or wobble, position of the codon. Recombination may be an underlying driving force given that recombination sites are often associated with high GC content. Here we explore the relationship between recombination and genomic GC patterns by comparing GC gene content at each of the three codon positions (GC1, GC2, and GC3, collectively termed GCx) to instances of a variable GC-rich motif that underlies double strand break (DSB) hotspots and to meiocyte-specific gene expression. Surprisingly, GCx bimodality in maize cannot be fully explained by the codon wobble hypothesis. High GCx genes show a strong overlap with the DSB hotspot motif, possibly providing a mechanism for the high evolutionary rates seen in these genes. On the other hand, genes that are turned on in meiosis (early prophase I) are biased against both high GCx genes and genes with the DSB hotspot motif, possibly allowing important meiotic genes to avoid DSBs. Our data suggests a strong link between the GC-rich motif underlying DSB hotspots and high GCx genes.http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01433/fullGene ExpressionMeiosisMaizerecombinationGCcodon usage
collection DOAJ
language English
format Article
sources DOAJ
author Anitha Sundararajan
Stefanie Dukowic-Schulze
Madeline Kwicklis
Kayla Engstrom
Nathan Garcia
Oliver J Oviedo
Thiruvarangan Ramaraj
Michael D Gonzales
Yan He
Minghui Wang
Minghui Wang
Qi Sun
Jaroslaw Pillardy
Shahryar F Kianian
Wojciech P Pawlowski
Changbin Chen
Joann Mudge
spellingShingle Anitha Sundararajan
Stefanie Dukowic-Schulze
Madeline Kwicklis
Kayla Engstrom
Nathan Garcia
Oliver J Oviedo
Thiruvarangan Ramaraj
Michael D Gonzales
Yan He
Minghui Wang
Minghui Wang
Qi Sun
Jaroslaw Pillardy
Shahryar F Kianian
Wojciech P Pawlowski
Changbin Chen
Joann Mudge
Gene evolutionary trajectories and GC patterns driven by recombination in Zea mays
Frontiers in Plant Science
Gene Expression
Meiosis
Maize
recombination
GC
codon usage
author_facet Anitha Sundararajan
Stefanie Dukowic-Schulze
Madeline Kwicklis
Kayla Engstrom
Nathan Garcia
Oliver J Oviedo
Thiruvarangan Ramaraj
Michael D Gonzales
Yan He
Minghui Wang
Minghui Wang
Qi Sun
Jaroslaw Pillardy
Shahryar F Kianian
Wojciech P Pawlowski
Changbin Chen
Joann Mudge
author_sort Anitha Sundararajan
title Gene evolutionary trajectories and GC patterns driven by recombination in Zea mays
title_short Gene evolutionary trajectories and GC patterns driven by recombination in Zea mays
title_full Gene evolutionary trajectories and GC patterns driven by recombination in Zea mays
title_fullStr Gene evolutionary trajectories and GC patterns driven by recombination in Zea mays
title_full_unstemmed Gene evolutionary trajectories and GC patterns driven by recombination in Zea mays
title_sort gene evolutionary trajectories and gc patterns driven by recombination in zea mays
publisher Frontiers Media S.A.
series Frontiers in Plant Science
issn 1664-462X
publishDate 2016-09-01
description Recombination occurring during meiosis is critical for creating genetic variation and plays an essential role in plant evolution. In addition to creating novel gene combinations, recombination can affect genome structure through altering GC patterns. In maize (Zea mays) and other grasses, another intriguing GC pattern exists. Maize genes show a bimodal GC content distribution that has been attributed to nucleotide bias in the third, or wobble, position of the codon. Recombination may be an underlying driving force given that recombination sites are often associated with high GC content. Here we explore the relationship between recombination and genomic GC patterns by comparing GC gene content at each of the three codon positions (GC1, GC2, and GC3, collectively termed GCx) to instances of a variable GC-rich motif that underlies double strand break (DSB) hotspots and to meiocyte-specific gene expression. Surprisingly, GCx bimodality in maize cannot be fully explained by the codon wobble hypothesis. High GCx genes show a strong overlap with the DSB hotspot motif, possibly providing a mechanism for the high evolutionary rates seen in these genes. On the other hand, genes that are turned on in meiosis (early prophase I) are biased against both high GCx genes and genes with the DSB hotspot motif, possibly allowing important meiotic genes to avoid DSBs. Our data suggests a strong link between the GC-rich motif underlying DSB hotspots and high GCx genes.
topic Gene Expression
Meiosis
Maize
recombination
GC
codon usage
url http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01433/full
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