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动态转录组分析揭示棉花中基因型顽固型体细胞胚胎发生转分化潜在的未知复杂调控途径。

Dynamic Transcriptome Analysis Reveals Uncharacterized Complex Regulatory Pathway Underlying Genotype-Recalcitrant Somatic Embryogenesis Transdifferentiation in Cotton.

作者信息

Guo Huihui, Guo Haixia, Zhang Li, Fan Yijie, Wu Jianfei, Tang Zhengmin, Zhang Yao, Fan Yupeng, Zeng Fanchang

机构信息

State Key Laboratory of Crop Biology, College of Agronomy, Shandong Agricultural University, Tai'an 271018, China.

出版信息

Genes (Basel). 2020 May 7;11(5):519. doi: 10.3390/genes11050519.

DOI:10.3390/genes11050519
PMID:32392816
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7290922/
Abstract

As a notable illustration of totipotency and plant regeneration, somatic embryogenesis (SE) is the developmental reprogramming of somatic cells toward the embryogenesis pathway, the key step for genetic engineering. Investigations examining the totipotency process are of great fundamental and practical importance in crop biotechnology. However, high-frequency regeneration of cotton via SE has been limited due to genotype-dependent response. The molecular basis deciphering SE genotype recalcitrance remains largely unexplored in cotton. In the current study, to comprehensively investigate the dynamic transcriptional profiling and gene regulatory patterns involved in SE process, a genome-wide RNA sequencing analysis was performed in two cotton genotypes with distinct embryogenic abilities, the highly embryogenic genotype Yuzao 1 (YZ) and the recalcitrant genotype Lumian 1 (LM). Three typical developmental staged cultures of early SE-hypocotyls (HY), nonembryogenic calli (NEC) and primary embryogenic calli (PEC)-were selected to establish the transcriptional profiles. Our data revealed that a total of 62,562 transcripts were present amongst different developmental stages in the two genotypes. Of these, 18,394 and 26,514 differentially expressed genes (DEGs) were identified during callus dedifferentiation (NEC-VS-HY) and embryogenic transdifferentiation (PEC-VS-NEC), respectively in the recalcitrant genotype, 21,842 and 22,343 DEGs in the highly embryogenic genotype. Furthermore, DEGs were clustered into six expression patterns during cotton SE process in the two genotypes. Moreover, functional enrichment analysis revealed that DEGs were significantly enriched in fatty acid, tryptophan and pyruvate metabolism in the highly embryogenic genotype and in DNA conformation change otherwise in the recalcitrant genotype. In addition, critical SE-associated expressed transcription factors, as well as alternative splicing events, were notably and preferentially activated during embryogenic transdifferentiation in the highly embryogenic genotype compared with the recalcitrant genotype. Taken together, by systematically comparing two genotypes with distinct embryogenic abilities, the findings in our study revealed a comprehensive overview of the dynamic gene regulatory patterns and uncharacterized complex regulatory pathways during cotton SE genotype-dependent response. Our work provides insights into the molecular basis and important gene resources for understanding the underlying genotype recalcitrance during SE process and plant regeneration, thereby holding great promise for accelerating the application of biotechnology to cotton for improving its breeding efficiency.

摘要

作为全能性和植物再生的一个显著例证,体细胞胚胎发生(SE)是体细胞向胚胎发生途径的发育重编程,是基因工程的关键步骤。研究全能性过程在作物生物技术中具有重要的基础和实际意义。然而,由于基因型依赖性反应,通过SE实现棉花的高频再生一直受到限制。在棉花中,破解SE基因型难培养性的分子基础在很大程度上仍未得到探索。在本研究中,为了全面研究SE过程中涉及的动态转录谱和基因调控模式,对两种具有不同胚胎发生能力的棉花基因型进行了全基因组RNA测序分析,即高胚胎发生能力的基因型豫早1号(YZ)和难培养基因型鲁棉1号(LM)。选择早期SE下胚轴(HY)、非胚性愈伤组织(NEC)和初级胚性愈伤组织(PEC)这三个典型发育阶段的培养物来建立转录谱。我们的数据显示,两种基因型的不同发育阶段共有62,562个转录本。其中,在难培养基因型的愈伤组织去分化(NEC-VS-HY)和胚性转分化(PEC-VS-NEC)过程中,分别鉴定出18,394个和26,514个差异表达基因(DEG),在高胚胎发生能力基因型中分别为21,842个和22,343个DEG。此外,在两种基因型的棉花SE过程中,DEG被聚类为六种表达模式。而且,功能富集分析表明,在高胚胎发生能力基因型中,DEG显著富集于脂肪酸、色氨酸和丙酮酸代谢,而在难培养基因型中则显著富集于DNA构象变化。此外,与难培养基因型相比,在高胚胎发生能力基因型的胚性转分化过程中,关键的SE相关表达转录因子以及可变剪接事件被显著且优先激活。综上所述,通过系统比较两种具有不同胚胎发生能力的基因型,我们的研究结果揭示了棉花SE基因型依赖性反应过程中动态基因调控模式和未表征的复杂调控途径的全面概况。我们的工作为理解SE过程和植物再生过程中潜在的基因型难培养性提供了分子基础和重要的基因资源,从而为加速生物技术在棉花上的应用以提高其育种效率带来了巨大希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/ad855d723727/genes-11-00519-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/84c61fc0e37d/genes-11-00519-g0A1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/8360f7d79bed/genes-11-00519-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/8a47be3315a9/genes-11-00519-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/61a43e24a45f/genes-11-00519-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/66b96d93c02f/genes-11-00519-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/ad855d723727/genes-11-00519-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/84c61fc0e37d/genes-11-00519-g0A1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/8360f7d79bed/genes-11-00519-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/8a47be3315a9/genes-11-00519-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/61a43e24a45f/genes-11-00519-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/66b96d93c02f/genes-11-00519-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f24d/7290922/ad855d723727/genes-11-00519-g005.jpg

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