Multi-Omics Analysis of Gene and microRNA Expression in Diploid and Autotetraploid Poplar under Drought Stress by Transcriptome, microRNA, and Degradome Sequencing

Abstract

Drought-induced forest death has become a global phenomenon, which is hindering the development of sustainable forestry. Polyploidy breeding has been considered as an effective method of genetic improvement for tree stress resistance. However, the response mechanisms of tetraploid poplars to drought stress are unclear. In this study, based on high-throughput sequencing of transcriptome, small RNA, and degradome for these samples, which selected three genotypes of tetraploid poplars and their counterpart diploids for drought stress and rewatering trial in the experiment, we performed multi-omics analyses to investigate the distinction in drought resistance between tetraploid and diploid. A total of 3391 differentially expressed genes (DEGs) were found from the Dro-Di vs. CK-Di, 3753 DEGs from the Re-Di vs. Dro-Di, 3857 DEGs from the Dro-Te vs. CK-Te, and 4177 DEGs from the Re-Te vs. Dro-Te. Of the above DEGs, 1646 common-DEGs were identified significantly related to drought-stress response, 2034 common-DEGs related to rewater response, 158 and 114 common-DEGs showed opposite expression patterns between diploid and tetraploid, implying that these DEGs might play important roles in response to drought stress as a result of differences in ploidy. Additionally, 586 known miRNAs and 72 novel miRNAs were identified through analysis of 18 small RNA libraries, among which eight common-miRNAs were significantly related to drought-stress response, and four were related to rewater response. The degradome sequencing analysis revealed that 154 target transcripts for 24 drought-stress-associated differentially expressed miRNAs (DEmiRs), and 90 for 12 rewatering-associated DEmiRs were identified in the tetraploid based on both degradome and TargetFinder analyses. These findings provide valuable information for further functional characterization of genes and miRNAs in response to drought stress in Populus polyploidy, and potentially contribute to drought-resistant breeding of polypoid in the future.