Characterization and Fine Mapping of a Novel Rice Narrow Leaf Mutant nal9

被引:51
|
作者
Li, Wei [1 ,3 ]
Wu, Chao [1 ,2 ]
Hu, Guocheng [1 ]
Xing, Li [1 ,3 ]
Qian, Wenjing [1 ,4 ]
Si, Huamin [1 ]
Sun, Zongxiu [1 ]
Wang, Xingchun [3 ]
Fu, Yaping [1 ]
Liu, Wenzhen [1 ]
机构
[1] China Natl Rice Res Inst, State Key Lab Rice Biol, Hangzhou 310006, Zhejiang, Peoples R China
[2] Zhejiang Acad Agr Sci, Inst Hort, Hangzhou 310021, Zhejiang, Peoples R China
[3] Shanxi Agr Univ, Coll Life Sci, Taigu 030801, Peoples R China
[4] China Three Gorges Univ, Biotechnol Res Ctr, Yichang 443002, Peoples R China
基金
中国国家自然科学基金;
关键词
Rice; narrow leaf; mutant; nal9; fine mapping; GENE; AUXIN; ARABIDOPSIS; TRANSPORT; PROTEASE; TISSUE; PLANTS;
D O I
10.1111/jipb.12098
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A narrow leaf mutant was isolated from transgenic rice (Oryza sativa L.) lines carrying a T-DNA insertion. The mutant is characterized by narrow leaves during its whole growth period, and was named nal9 (narrow leaf 9). The mutant also has other phenotypes, such as light green leaves at the seedling stage, reduced plant height, a small panicle and increased tillering. Genetic analysis revealed that the mutation is controlled by a single recessive gene. A hygromycin resistance assay showed that the mutation was not caused by T-DNA insertion, so a map-based cloning strategy was employed to isolate the nal9 gene. The mutant individuals from the F-2 generations of a cross between the nal9 mutant and Longtepu were used for mapping. With 24 F-2 mutants, the nal9 gene was preliminarily mapped near the marker RM156 on the chromosome 3. New INDEL markers were then designed based on the sequence differences between japonica and indica at the region near RM156. The nal9 gene was finally located in a 69.3kb region between the markers V239B and V239G within BAC OJ1212_C05 by chromosome walking. Sequence and expression analysis showed that an ATP-dependent Clp protease proteolytic subunit gene (ClpP) was most likely to be the nal9 gene. Furthermore, the nal9 mutation was rescued by transformation of the ClpP cDNA driven by the 35S promoter. Accordingly, the ClpP gene was identified as the NAL9 gene. Our results provide a basis for functional studies of NAL9 in future work.
引用
收藏
页码:1016 / 1025
页数:10
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