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...
Main Authors: | , , , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2016-09-01
|
Series: | Frontiers in Plant Science |
Subjects: | |
Online Access: | http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01433/full |
id |
doaj-c95da4924f7b4a738fb874a93079817b |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT anithasundararajan geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT stefaniedukowicschulze geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT madelinekwicklis geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT kaylaengstrom geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT nathangarcia geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT oliverjoviedo geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT thiruvaranganramaraj geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT michaeldgonzales geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT yanhe geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT minghuiwang geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT minghuiwang geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT qisun geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT jaroslawpillardy geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT shahryarfkianian geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT wojciechppawlowski geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT changbinchen geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays AT joannmudge geneevolutionarytrajectoriesandgcpatternsdrivenbyrecombinationinzeamays |
_version_ |
1725971495558053888 |