AUTHOR=Sundararajan Anitha , Dukowic-Schulze Stefanie , Kwicklis Madeline , Engstrom Kayla , Garcia Nathan , Oviedo Oliver J. , Ramaraj Thiruvarangan , Gonzales Michael D. , He Yan , Wang Minghui , Sun Qi , Pillardy Jaroslaw , Kianian Shahryar F. , Pawlowski Wojciech P. , Chen Changbin , Mudge Joann TITLE=Gene Evolutionary Trajectories and GC Patterns Driven by Recombination in Zea mays JOURNAL=Frontiers in Plant Science VOLUME=7 YEAR=2016 URL=https://www.frontiersin.org/journals/plant-science/articles/10.3389/fpls.2016.01433 DOI=10.3389/fpls.2016.01433 ISSN=1664-462X ABSTRACT=

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.