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细胞学分析与 paa1(花粉后异常花药 1)突变体的精细定位,该突变体表现为绒毡层和小孢子发育异常。

Cytological Analysis and Fine Mapping of paa1 (Post-meiosis Abnormal Anther 1) Mutant with Abnormal Tapetum and Microspore Development.

机构信息

Key Laboratory of Crop Physiology Ecology and Genetic Breeding Ministry of Education, Jiangxi Agricultural University, Nanchang, 330045, China.

College of Bioscience and Bioengineering, Jiangxi Agricultural University, Nanchang, 330045, China.

出版信息

Biochem Genet. 2022 Dec;60(6):2268-2285. doi: 10.1007/s10528-022-10217-4. Epub 2022 Mar 24.

DOI:10.1007/s10528-022-10217-4
PMID:35325440
Abstract

To further understand the molecular mechanism for rice male reproduction, a rice male sterile mutant paa1 was screened from the rice mutant library generated by treatment with Coγ-rays. Genetic analysis revealed that paa1 is controlled by a single- recessive nuclear gene, and the anthers of the paa1 mutant were smaller than those of WT plants with a white color. Histological analysis demonstrated that the anthers of the paa1 mutant began to turn abnormal at the microspore stage after meiosis, with abnormal degradation of tapetum, deformed Ubisch bodies, and defective pollen exine. TUNEL assay results also confirmed the delay of tapetum PCD in paa1. Map-based cloning was performed for the PAA1 location. As a result, PAA1 was located in a 88-kb region at the end of chromosome 10, which comprises a total of seven candidate genes, and no genes related to anther development have been reported in this region. The results indicate that PAA1 is an essential gene in regulating tapetum development and pollen/microspore formation after rice meiosis.

摘要

为了进一步了解水稻雄性生殖的分子机制,我们从 Coγ射线处理生成的水稻突变体库中筛选出一个水稻雄性不育突变体 paa1。遗传分析表明,paa1 由一个单隐性核基因控制,其花药小于 WT 植株的花药,呈白色。组织学分析表明,paa1 突变体的花药在减数分裂后小孢子阶段开始出现异常,绒毡层异常降解,Ubiisch 体变形,花粉外壁缺陷。TUNEL 检测结果也证实了 paa1 中绒毡层 PCG 的延迟。我们对 PAA1 位置进行了基于图谱的克隆。结果表明,PAA1 位于第 10 号染色体末端的 88kb 区域内,共包含七个候选基因,而在该区域尚未报道与花药发育相关的基因。这些结果表明 PAA1 是一个调控水稻减数分裂后绒毡层发育和花粉/小孢子形成的必需基因。

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本文引用的文献

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Theor Appl Genet. 2021 Feb;134(2):453-471. doi: 10.1007/s00122-020-03706-w. Epub 2020 Oct 21.
2
Rice pollen aperture formation is regulated by the interplay between OsINP1 and OsDAF1.水稻花粉孔的形成受 OsINP1 和 OsDAF1 相互作用的调节。
Nat Plants. 2020 Apr;6(4):394-403. doi: 10.1038/s41477-020-0630-6. Epub 2020 Apr 13.
3
OsMYB80 Regulates Anther Development and Pollen Fertility by Targeting Multiple Biological Pathways.
OsMYB80 通过靶向多个生物学途径调控花药发育和花粉育性。
Plant Cell Physiol. 2020 May 1;61(5):988-1004. doi: 10.1093/pcp/pcaa025.
4
Lectin receptor kinase OsLecRK-S.7 is required for pollen development and male fertility.凝集素受体激酶 OsLecRK-S.7 对于花粉发育和雄性育性是必需的。
J Integr Plant Biol. 2020 Aug;62(8):1227-1245. doi: 10.1111/jipb.12897. Epub 2020 Mar 6.
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PERSISTENT TAPETAL CELL2 Is Required for Normal Tapetal Programmed Cell Death and Pollen Wall Patterning.持久绒毡层细胞 2 对于正常绒毡层程序性细胞死亡和花粉外壁纹饰形成是必需的。
Plant Physiol. 2020 Feb;182(2):962-976. doi: 10.1104/pp.19.00688. Epub 2019 Nov 26.
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Mutation of the chloroplast-localized phosphate transporter OsPHT2;1 reduces flavonoid accumulation and UV tolerance in rice.叶绿体定位的磷酸盐转运蛋白 OsPHT2;1 的突变降低了水稻中类黄酮的积累和对紫外线的耐受性。
Plant J. 2020 Apr;102(1):53-67. doi: 10.1111/tpj.14611. Epub 2019 Dec 22.
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