Transcription Profile Analysis of Chlorophyll Biosynthesis in Leaves of Wild-Type and Chlorophyll b-Deficient Rice (Oryza sativa L.)

被引:6
|
作者
Minh Khiem Nguyen [1 ,2 ,3 ,4 ,5 ]
Shih, Tin-Han [3 ]
Lin, Szu-Hsien [3 ]
Lin, Jun-Wei [3 ]
Hoang Chinh Nguyen [5 ]
Yang, Zhi-Wei [6 ]
Yang, Chi-Ming [1 ,2 ,3 ]
机构
[1] Acad Sinica, Biodivers Res Ctr, Taiwan Int Grad Program, Biodivers Program, Taipei 115, Taiwan
[2] Natl Taiwan Normal Univ, Taipei 115, Taiwan
[3] Acad Sinica, Biodivers Res Ctr, Taipei 115, Taiwan
[4] Natl Taiwan Normal Univ, Dept Life Sci, Taipei 116, Taiwan
[5] Ton Duc Thang Univ, Fac Appl Sci, Ho Chi Minh City 700000, Vietnam
[6] Council Agr, Taoyuan Dist Agr Res & Extens Stn, Taoyuan 327, Taiwan
来源
AGRICULTURE-BASEL | 2021年 / 11卷 / 05期
关键词
Chl b-deficient mutant; photosynthesis; RNA-Seq transcriptome; PHOTOSYSTEM-I; LEAF COLOR; PROTEIN-PHOSPHORYLATION; CHLOROPLAST DEVELOPMENT; ARABIDOPSIS-THALIANA; THYLAKOID MEMBRANE; ANALYSIS REVEALS; MUTANTS; PHOTOSYNTHESIS; GENE;
D O I
10.3390/agriculture11050401
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Photosynthesis is an essential biological process and a key approach for raising crop yield. However, photosynthesis in rice is not fully investigated. This study reported the photosynthetic properties and transcriptomic profiles of chlorophyll (Chl) b-deficient mutant (ch11) and wild-type rice (Oryza sativa L.). Chl b-deficient rice revealed irregular chloroplast development (indistinct membranes, loss of starch granules, thinner grana, and numerous plastoglobuli). Next-generation sequencing approach application revealed that the differential expressed genes were related to photosynthesis machinery, Chl-biosynthesis, and degradation pathway in ch11. Two genes encoding PsbR (PSII core protein), FtsZ1, and PetH genes, were found to be down-regulated. The expression of the FtsZ1 and PetH genes resulted in disrupted chloroplast cell division and electron flow, respectively, consequently reducing Chl accumulation and the photosynthetic capacity of Chl b-deficient rice. Furthermore, this study found the up-regulated expression of the GluRS gene, whereas the POR gene was down-regulated in the Chl biosynthesis and degradation pathways. The results obtained from RT-qPCR analyses were generally consistent with those of transcription analysis, with the exception of the finding that MgCH genes were up-regulated which enhance the important intermediate products in the Mg branch of Chl biosynthesis. These results indicate a reduction in the accumulation of both Chl a and Chl b. This study suggested that a decline in Chl accumulation is caused by irregular chloroplast formation and down-regulation of POR genes; and Chl b might be degraded via the pheophorbide b pathway, which requires further elucidation.
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页数:17
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