4.6 Article

Asymmetric Somatic Hybridization Affects Synonymous Codon Usage Bias in Wheat

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FRONTIERS IN GENETICS
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2021.682324

关键词

introgression line; genomic shock; synonymous codon usage bias; somatic hybridization; wheat

资金

  1. National Key Research and Development Project [2016YFD0102003]
  2. National Natural Science Foundation of China [31870242, 31800214]
  3. Shandong Province's Key Research and Development [2018GNC110010]
  4. Natural Science Foundation of Shandong Province [ZR2019BC061]

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Asymmetric somatic hybridization affects synonymous codon usage bias (SCUB) and promotes a bias towards A- and T-ending synonymous codons, with a stronger effect in indel-flanking sequences. This shift is attributed to whole genomic shock, and DNA methylation may play a role in SCUB shift during asymmetric somatic hybridization. Exogenous chromatin fragments introduced through this strategy do not have a local chromosomal effect on SCUB frequencies.
Asymmetric somatic hybridization is an efficient strategy for crop breeding by introducing exogenous chromatin fragments, which leads to whole genomic shock and local chromosomal shock that induces genome-wide genetic variation including indel (insertion and deletion) and nucleotide substitution. Nucleotide substitution causes synonymous codon usage bias (SCUB), an indicator of genomic mutation and natural selection. However, how asymmetric somatic hybridization affects SCUB has not been addressed. Here, we explored this issue by comparing expressed sequence tags of a common wheat cultivar and its asymmetric somatic hybrid line. Asymmetric somatic hybridization affected SCUB and promoted the bias to A- and T-ending synonymous codon (SCs). SCUB frequencies in chromosomes introgressed with exogenous fragments were comparable to those in chromosomes without exogenous fragments, showing that exogenous fragments had no local chromosomal effect. Asymmetric somatic hybridization affected SCUB frequencies in indel-flanking sequences more strongly than in non-flanking sequences, and this stronger effect was present in both chromosomes with and without exogenous fragments. DNA methylation-driven SCUB shift was more pronounced than other SC pairs. SCUB shift was similar among seven groups of allelic chromosomes as well as three sub-genomes. Our work demonstrates that the SCUB shift induced by asymmetric somatic hybridization is attributed to the whole genomic shock, and DNA methylation is a putative force of SCUB shift during asymmetric somatic hybridization. Asymmetric somatic hybridization provides an available method for deepening the nature of SCUB shift and genetic variation induced by genomic shock.

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