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Transcriptome Analysis of Floral Buds Deciphered an Irregular Course of Meiosis in Polyploid Brassica rapa

机译:转录组分析的花蕾破译多倍体油菜的减数分裂的不规则过程。

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摘要

Polyploidy is a fundamental process in plant evolution. Understanding the polyploidy-associated effects on plant reproduction is essential for polyploid breeding program. In the present study, our cytological analysis firstly demonstrated that an overall course of meiosis was apparently distorted in the synthetic polyploid Brassica rapa in comparison with its diploid progenitor. To elucidate genetic basis of this irregular meiosis at a molecular level, the comparative RNA-seq analysis was further used to investigate differential genetic regulation of developing floral buds identified at meiosis between autotetraploid and diploid B. rapa. In total, compared to its diploid counterparts, among all 40,927 expressed genes revealed, 4,601 differentially expressed genes (DEGs) were identified in the floral buds of autotetraploid B. rapa, among which 288 DEGs annotated were involved in meiosis. Notably, DMC1 identified as one previously known meiosis-specific gene involved in inter-homologous chromosome dependent repair of DNA double stranded breaks (DSBs), was significantly down-regulated in autotetraploid B. rapa, which presumably contributed to abnormal progression during meiosis I. Although certain DEGs associated with RNA helicase, cell cycling, and somatic DNA repair were up-regulated after genome duplication, genes associated with meiotic DSB repair were significantly down-regulated. Furthermore, the expression of randomly selected DEGs by RNA-seq analysis was confirmed by quantitative real-time PCR analysis in both B. rapa and Arabidopsis thaliana. Our results firstly account for adverse effects of polyploidy on an entire course of meiosis at both cytological and transcriptomic levels, and allow for a comprehensive understanding of the uniformity and differences in the transcriptome of floral buds at meiosis between diploid and polyploid B. rapa as well.
机译:多倍体是植物进化的基本过程。了解多倍体对植物繁殖的影响对于多倍体育种计划至关重要。在本研究中,我们的细胞学分析首先表明,与二倍体祖细胞相比,合成的多倍体芸苔中减数分裂的整个过程明显变形。为了在分子水平上阐明这种不规则减数分裂的遗传基础,比较RNA-seq分析进一步用于研究在同源四倍体和二倍体B. rapa减数分裂中鉴定出的发育中的花芽的差异遗传调控。与二倍体相对应,总共揭示了40,927个表达基因,在同源四倍体B. rapa的花芽中鉴定出4,601个差异表达基因(DEG),其中288个带注释的DEG与减数分裂有关。值得注意的是,DMC1被鉴定为一种参与DNA双链断裂(DSBs)同源染色体间依赖修复的减数分裂特异性基因,在同源四倍体B.rapa中显着下调,这可能导致减数分裂I期间的异常进展。尽管在基因组复制后某些与RNA解旋酶,细胞周期和体细胞DNA修复相关的DEGs上调,但与减数分裂DSB修复相关的基因却显着下调。此外,通过定量实时PCR分析证实了在芥菜和拟南芥中通过RNA-seq分析随机选择的DEG的表达。我们的研究结果首先说明了多倍体在整个减数分裂过程中在细胞学和转录组水平上的不利影响,并且使我们能够全面了解二倍体和多倍体B. rapa减数分裂上花蕾的转录组的一致性和差异。 。

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