Title The alteration in the architecture of a T-DNA insertion rice mutant osmtd1 is caused by up-regulation of MicroRNA156f
Authors Liu, Qing
Shen, Gezhi
Peng, Keqin
Huang, Zhigang
Tong, Jianhua
Kabir, Mohammed Humayun
Wang, Jianhui
Zhang, Jingzhe
Qin, Genji
Xiao, Langtao
Affiliation Hunan Agr Univ, Hunan Prov Key Lab Phytohormones & Growth Dev, Hunan Prov Key Lab Crop Germplasm Innovat & Utili, Changsha 410128, Peoples R China.
Shanghai Acad Agr Sci, Crop Inst, Shanghai 201106, Peoples R China.
Sichuan Acad Agr Sci, Inst Hort, Chengdu 610066, Peoples R China.
Peking Univ, Coll Life Sci, State Key Lab Prot & Plant Gene Res, Beijing 100871, Peoples R China.
Keywords Oryza sativa
OsmiR156f
plant architecture
protease inhibitor
T-DNA insertion
PLANT ARCHITECTURE
TRANSCRIPTION FACTORS
NEGATIVE REGULATION
PROTEASE INHIBITOR
SHOOT GRAVITROPISM
BUD OUTGROWTH
PHASE-CHANGE
MONOCULM 1
ARABIDOPSIS
GENE
Issue Date 2015
Publisher JOURNAL OF INTEGRATIVE PLANT BIOLOGY
Citation JOURNAL OF INTEGRATIVE PLANT BIOLOGY.2015,57,(10),819-829.
Abstract Plant architecture is an important factor for crop production. Some members of microRNA156 (miR156) and their target genes SQUAMOSAPromoter-Binding Protein-Like (SPL) were identified to play essential roles in the establishment of plant architecture. However, the roles and regulation of miR156 is not well understood yet. Here, we identified a T-DNA insertion mutant Osmtd1 (Oryza sativa multi-tillering and dwarf mutant). Osmtd1 produced more tillers and displayed short stature phenotype. We determined that the dramatic morphological changes were caused by a single T-DNA insertion in Osmtd1. Further analysis revealed that the T-DNA insertion was located in the gene Os08g34258 encoding a putative inhibitor I family protein. Os08g34258 was knocked out and OsmiR156f was significantly upregulated in Osmtd1. Overexpression of Os08g34258 in Osmtd1 complemented the defects of the mutant architecture, while overexpression of OsmiR156f in wild-type rice phenocopied Osmtd1. We showed that the expression of OsSPL3, OsSPL12, and OsSPL14 were significantly downregulated in Osmtd1 or OsmiR156f overexpressed lines, indicating that OsSPL3, OsSPL12, and OsSPL14 were possibly direct target genes of OsmiR156f. Our results suggested that OsmiR156f controlled plant architecture by mediating plant stature and tiller outgrowth and may be regulated by an unknown protease inhibitor I family protein.
URI http://hdl.handle.net/20.500.11897/415934
ISSN 1672-9072
DOI 10.1111/jipb.12340
Indexed SCI(E)
PubMed
中国科技核心期刊(ISTIC)
中国科学引文数据库(CSCD)
Appears in Collections: 生命科学学院

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