State Key Laboratory of North China Crop Improvement and Regulation, North China Key Laboratory for Crop Germplasm Resources of Education Ministry, Hebei Agricultural University, Baoding, 071001, China.
BMC Plant Biol. 2022 Jan 3;22(1):6. doi: 10.1186/s12870-021-03382-y.
The fiber yield and quality of cotton are greatly and periodically affected by water deficit. However, the molecular mechanism of the water deficit response in cotton fiber cells has not been fully elucidated.
In this study, water deficit caused a significant reduction in fiber length, strength, and elongation rate but a dramatic increase in micronaire value. To explore genome-wide transcriptional changes, fibers from cotton plants subjected to water deficit (WD) and normal irrigation (NI) during fiber development were analyzed by transcriptome sequencing. Analysis showed that 3427 mRNAs and 1021 long noncoding RNAs (lncRNAs) from fibers were differentially expressed between WD and NI plants. The maximum number of differentially expressed genes (DEGs) and lncRNAs (DERs) was identified in fibers at the secondary cell wall biosynthesis stage, suggesting that this is a critical period in response to water deficit. Twelve genes in cotton fiber were differentially and persistently expressed at ≥ five time points, suggesting that these genes are involved in both fiber development and the water-deficit response and could potentially be used in breeding to improve cotton resistance to drought stress. A total of 540 DEGs were predicted to be potentially regulated by DERs by analysis of coexpression and genomic colocation, accounting for approximately 15.76% of all DEGs. Four DERs, potentially acting as target mimics for microRNAs (miRNAs), indirectly regulated their corresponding DEGs in response to water deficit.
This work provides a comprehensive transcriptome analysis of fiber cells and a set of protein-coding genes and lncRNAs implicated in the cotton response to water deficit, significantly affecting fiber quality during the fiber development stage.
棉花的纤维产量和品质会受到水分亏缺的显著且周期性的影响。然而,棉花纤维细胞水分亏缺响应的分子机制尚未完全阐明。
本研究中,水分亏缺导致纤维长度、强度和伸长率显著降低,而马克隆值显著增加。为了探究全基因组转录变化,对纤维发育过程中经历水分亏缺(WD)和正常灌溉(NI)的棉花植株的纤维进行转录组测序分析。分析表明,WD 和 NI 植株的纤维中有 3427 个 mRNA 和 1021 个长非编码 RNA(lncRNA)差异表达。差异表达基因(DEGs)和 lncRNA(DERs)数量最多的时期是次生细胞壁生物合成期,表明这是对水分亏缺响应的关键时期。在≥5 个时间点,棉花纤维中有 12 个基因差异且持续表达,表明这些基因既参与纤维发育,又参与水分亏缺响应,可能被用于培育来提高棉花对干旱胁迫的抗性。通过共表达和基因组共定位分析,预测到 540 个 DEG 可能受到 DERs 的调控,约占所有 DEG 的 15.76%。4 个 DERs 可能作为 microRNAs(miRNAs)的靶标模拟物,间接调节其对应的 DEG 来响应水分亏缺。
本研究为纤维细胞提供了全面的转录组分析,以及一组与棉花水分亏缺响应相关的蛋白质编码基因和 lncRNA,这些基因在纤维发育阶段显著影响纤维品质。