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Chuxiong Zhuang
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, College of Life Sciences, South China Agricultural University
Corresponding Author
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Most pentatricopeptide repeat (PPR) proteins localize to plastids or mitochondria, where they participate in RNA metabolism and post-transcriptionally regulate organelle gene expression. However, whether PPR proteins regulate the expression of nucleus-encoded genes remains unclear. Here, we uncovered a function for the rice (Oryza. sativa L.) PPR protein OsPPR2-1 (Os02g0110400) in pollen development and showed that, in contrast to most other PPR proteins, OPPR2-1 resides in the cytoplasm. Downregulating OsPPR2-1 expression led to abnormal plastid development in tapetal cells, prolonged programmed cell death (PCD), prolonged tapetum degradation, and significantly reduced pollen fertility. Transcriptome analysis revealed that the expression of OsGOLDEN-LIKE 1 (OsGLK1), encoding a transcription factor that regulates plastid development and maintenance, was significantly higher in plants with downregulated OsPPR2-1 expression compared to the wild type. Moreover, OsPPR2-1 bound to the OsGLK1 mRNA in RNA immunoprecipitation and RNA-electrophoretic mobility shift assays. An in vitro cleavage assay showed that OsPPR2-1 could degrade the OsGLK1 mRNA. Notably, knockdown of OsGLK1 partially restored pollen fertility in OsPPR2-1-knockdown plants and OsGLK1-overexpressing plants showed abnormal tapetum and plastid development, similar to the OsPPR2-1-knockdown plants. Together, our findings demonstrate that OsPPR2-1 regulates OsGLK1 expression, thereby controlling plastid development and PCD in the tapetum.
Keywords
OsPPR2-1, tapetum, PCD, plastid, OsGLK1
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This is a preprint, a preliminary version of a manuscript that has not completed peer review at a journal. Research Square does not conduct peer review prior to posting preprints. The posting of a preprint on this server should not be interpreted as an endorsement of its validity or suitability for dissemination as established information or for guiding clinical practice.
Article
Chuxiong Zhuang
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, College of Life Sciences, South China Agricultural University
Corresponding Author
Badges
Prescreen
This manuscript passed our Prescreen assessment
Complete author information
Appropriate declaration statements
Potential risks to human health
Prescreen
History
CURRENT STATUS: Posted
Version 1
Posted 29 Jan, 2021
No community comments so far
Metrics
Comments: 0
PDF Downloads: ...
HTML Views: ...
License:
This work is licensed under a CC BY 4.0 License. Read Full License
Most pentatricopeptide repeat (PPR) proteins localize to plastids or mitochondria, where they participate in RNA metabolism and post-transcriptionally regulate organelle gene expression. However, whether PPR proteins regulate the expression of nucleus-encoded genes remains unclear. Here, we uncovered a function for the rice (Oryza. sativa L.) PPR protein OsPPR2-1 (Os02g0110400) in pollen development and showed that, in contrast to most other PPR proteins, OPPR2-1 resides in the cytoplasm. Downregulating OsPPR2-1 expression led to abnormal plastid development in tapetal cells, prolonged programmed cell death (PCD), prolonged tapetum degradation, and significantly reduced pollen fertility. Transcriptome analysis revealed that the expression of OsGOLDEN-LIKE 1 (OsGLK1), encoding a transcription factor that regulates plastid development and maintenance, was significantly higher in plants with downregulated OsPPR2-1 expression compared to the wild type. Moreover, OsPPR2-1 bound to the OsGLK1 mRNA in RNA immunoprecipitation and RNA-electrophoretic mobility shift assays. An in vitro cleavage assay showed that OsPPR2-1 could degrade the OsGLK1 mRNA. Notably, knockdown of OsGLK1 partially restored pollen fertility in OsPPR2-1-knockdown plants and OsGLK1-overexpressing plants showed abnormal tapetum and plastid development, similar to the OsPPR2-1-knockdown plants. Together, our findings demonstrate that OsPPR2-1 regulates OsGLK1 expression, thereby controlling plastid development and PCD in the tapetum.
Figure 1
Figure 2
Figure 3
Figure 4
Figure 5
Figure 6
Figure 7
The full text of this article is available to read as a PDF.
There is NO Competing Interest.
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