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Illegitimate Recombination between Duplicated Genes Generated from Recursive Polyploidizations Accelerated the Divergence of the Genus Arachis .

Shaoqi ShenYuxian LiJianyu WangChendan WeiZhenyi WangWeina GeMin YuanLan ZhangLi WangSangrong SunJia TengQimeng XiaoShoutong BaoYishan FengYan ZhangJiaqi WangYanan HaoTianyu LeiJin-Peng Wang
Published in: Genes (2021)
The peanut ( Arachis hypogaea L.) is the leading oil and food crop among the legume family. Extensive duplicate gene pairs generated from recursive polyploidizations with high sequence similarity could result from gene conversion, caused by illegitimate DNA recombination. Here, through synteny-based comparisons of two diploid and three tetraploid peanut genomes, we identified the duplicated genes generated from legume common tetraploidy (LCT) and peanut recent allo-tetraploidy (PRT) within genomes. In each peanut genome (or subgenomes), we inferred that 6.8-13.1% of LCT-related and 11.3-16.5% of PRT-related duplicates were affected by gene conversion, in which the LCT-related duplicates were the most affected by partial gene conversion, whereas the PRT-related duplicates were the most affected by whole gene conversion. Notably, we observed the conversion between duplicates as the long-lasting contribution of polyploidizations accelerated the divergence of different Arachis genomes. Moreover, we found that the converted duplicates are unevenly distributed across the chromosomes and are more often near the ends of the chromosomes in each genome. We also confirmed that well-preserved homoeologous chromosome regions may facilitate duplicates' conversion. In addition, we found that these biological functions contain a higher number of preferentially converted genes, such as catalytic activity-related genes. We identified specific domains that are involved in converted genes, implying that conversions are associated with important traits of peanut growth and development.
Keyphrases
  • genome wide
  • genome wide identification
  • copy number
  • dna methylation
  • genome wide analysis
  • transcription factor
  • dna damage
  • climate change
  • gene expression
  • dna repair
  • bioinformatics analysis
  • single molecule