DCET1 Controls Male Sterility Through Callose Regulation, Exine Formation, and Tapetal Programmed Cell Death in Rice

In angiosperms, anther development comprises of various complex and interrelated biological processes, critically needed for pollen viability. The transitory callose layer serves to separate the meiocytes. It helps in primexine formation, while the timely degradation of tapetal cells is essential fo...

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Veröffentlicht in:Frontiers in genetics 2021-11, Vol.12, p.790789
Hauptverfasser: Khan, Riaz Muhammad, Yu, Ping, Sun, Lianping, Abbas, Adil, Shah, Liaqat, Xiang, Xiaojiao, Wang, Dongfei, Sohail, Amir, Zhang, Yingxin, Liu, Qunen, Cheng, Shihua, Cao, Liyong
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Sprache:eng
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Zusammenfassung:In angiosperms, anther development comprises of various complex and interrelated biological processes, critically needed for pollen viability. The transitory callose layer serves to separate the meiocytes. It helps in primexine formation, while the timely degradation of tapetal cells is essential for the timely callose wall dissolution and pollen wall formation by providing nutrients for pollen growth. In rice, many genes have been reported and functionally characterized that are involved in callose regulation and pollen wall patterning, including timely programmed cell death (PCD) of the tapetum, but the mechanism of pollen development largely remains ambiguous. We identified and functionally characterized a rice mutant , having a complete male-sterile phenotype caused by defects in anther callose wall, exine patterning, and tapetal PCD. belongs to the RNA recognition motif (RRM)-containing family also called as the ribonucleoprotein (RNP) domain or RNA-binding domain (RBD) protein, having single-nucleotide polymorphism (SNP) substitution from G (threonine-192) to A (isoleucine-192) located at the fifth exon of LOC_Os08g02330, was responsible for the male sterile phenotype in mutant . Our cytological analysis suggested that regulates callose biosynthesis and degradation, pollen exine formation by affecting exine wall patterning, including abnormal nexine, collapsed bacula, and irregular tectum, and timely PCD by delaying the tapetal cell degeneration. As a result, the microspore of was swollen and abnormally bursted and even collapsed within the anther locule characterizing complete male sterility. GUS and qRT-PCR analysis indicated that is specifically expressed in the anther till the developmental stage 9, consistent with the observed phenotype. The characterization of in callose regulation, pollen wall patterning, and tapetal cell PCD strengthens our knowledge for knowing the regulatory pathways involved in rice male reproductive development and has future prospects in hybrid rice breeding.
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2021.790789