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综合细胞学和转录组学分析为油菜合成异源四倍体花粉活力恢复提供了新的见解。

Integrated cytological and transcriptomic analyses provide new insights into restoration of pollen viability in synthetic allotetraploid Brassica carinata.

机构信息

Henan International Joint Laboratory of Crop Gene Resources and Improvements, School of Agricultural Sciences, Zhengzhou University, Zhengzhou, 450001, Henan, China.

Institute of Horticulture, Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Zhengzhou, 450002, Henan, China.

出版信息

Plant Cell Rep. 2024 Sep 18;43(10):234. doi: 10.1007/s00299-024-03325-5.

Abstract

Upregulation of genes involved in DNA damage repair and sperm cell differentiation leads to restoration of pollen viability in synthetic allotetraploid B. carinata after chromosome doubling. Apart from the well-known contribution of polyploidy to crop improvement, polyploids can also be induced for other purposes, such as to restore the viability of sterile hybrids. The mechanism related to viability transition between the sterile allodiploid and the fertile allotetraploid after chromosome doubling are not well understood. Here, we synthesised allodiploid B. carinata (2n = 2x = 17) and allotetraploid B. carinata (2n = 4x = 34) as models to investigate the cytological and transcriptomic differences during pollen development. The results showed that after chromosome doubling, the recovery of pollen viability in allotetraploid was mainly reflected in the stabilisation of microtubule spindle morphology, normal meiotic chromosome behaviour, and normal microspore development. Interestingly, the deposition and degradation of synthetic anther tapetum were not affected by polyploidy. Transcription analysis showed that the expression of genes related to DNA repair (DMC1, RAD51, RAD17, SPO11-2), cell cycle differentiation (CYCA1;2, CYCA2;3) and ubiquitination proteasome pathway (UBC4, PIRH2, CDC53) were positively up-regulated during pollen development of synthetic allotetraploid B. carinata. In summary, these results provide some refreshing updates about the ploidy-related restoration of pollen viability in newly synthesised allotetraploid B. carinata.

摘要

基因的上调参与 DNA 损伤修复和精子细胞分化导致合成的异源四倍体 B. carinata 在加倍染色体后花粉活力的恢复。除了多倍体对作物改良的众所周知的贡献外,还可以诱导多倍体用于其他目的,例如恢复不育杂种的活力。加倍染色体后不育的异源二倍体和可育的异源四倍体之间活力转变的相关机制尚不清楚。在这里,我们合成了异源二倍体 B. carinata(2n = 2x = 17)和异源四倍体 B. carinata(2n = 4x = 34)作为模型,以研究花粉发育过程中的细胞学和转录组差异。结果表明,加倍染色体后,异源四倍体花粉活力的恢复主要反映在微管纺锤体形态的稳定、正常的减数分裂染色体行为和正常的小孢子发育。有趣的是,合成花药绒毡层的沉积和降解不受多倍体的影响。转录分析表明,与 DNA 修复(DMC1、RAD51、RAD17、SPO11-2)、细胞周期分化(CYCA1;2、CYCA2;3)和泛素化蛋白酶体途径(UBC4、PIRH2、CDC53)相关的基因在合成的异源四倍体 B. carinata 的花粉发育过程中呈正上调表达。总之,这些结果为新合成的异源四倍体 B. carinata 中与倍性相关的花粉活力恢复提供了一些更新鲜的信息。

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