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Journal of Integrative Agriculture  2011, Vol. 10 Issue (12): 1825-1833    DOI: 10.1016/S1671-2927(11)60182-X
GENETICS & BREEDING · GERMPLASM RESOURCES · MOLECULAR GENETICS Advanced Online Publication | Current Issue | Archive | Adv Search |
Fine Mapping and Cloning of the Grain Number Per-Panicle Gene (Gnp4) on Chromosome 4 in Rice (Oryza sativa L.)
 ZHANG Zhan-ying, LI Jin-jie, YAO Guo-xin, ZHANG Hong-liang, DOU Hui-jing, SHI Hong-li, SUN Xingming, LI Zi-chao
1.Key Laboratory of Crop Heterosis and Utilization, Ministry of Agriculture/Beijing Key Laboratory of Crop Genetic Improvement, China Agricultural University, Beijing 100193, P.R.China
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摘要  Grain number per-panicle is one of the most important components for rice yield. Spikelets on the primary and secondary branches determine the grain number per-panicle in rice. In this study, we identified a natural mutant, gnp4, lack of lateral spikelet on the secondary branches in the field condition. In addition, the Gnp4 and Lax1-1 double mutant showed dramatically reduced secondary branches and spikelets in panicle at reproductive stage, and tillers at vegetative stage. By map-based cloning approach, and using four F2 segregating populations, the Gnp4 gene was finally mapped to a 10.7-kb region on the long arm of chromosome 4 in rice. In this region, only one gene was predicted, and genomic DNA sequencing of the 10.7-kb region showed no nucleotide differences between the mutant and wild type. Interestingly, we found that the methylation level of several cytosines in the promoter CpG islands region of the predicted gene in gnp4 were different from the wild type. Thus, we propose that the DNA methylation changes at these sites may induce to decrease expression level of Gnp4, consequently, resulting in phenotypic variation.

Abstract  Grain number per-panicle is one of the most important components for rice yield. Spikelets on the primary and secondary branches determine the grain number per-panicle in rice. In this study, we identified a natural mutant, gnp4, lack of lateral spikelet on the secondary branches in the field condition. In addition, the Gnp4 and Lax1-1 double mutant showed dramatically reduced secondary branches and spikelets in panicle at reproductive stage, and tillers at vegetative stage. By map-based cloning approach, and using four F2 segregating populations, the Gnp4 gene was finally mapped to a 10.7-kb region on the long arm of chromosome 4 in rice. In this region, only one gene was predicted, and genomic DNA sequencing of the 10.7-kb region showed no nucleotide differences between the mutant and wild type. Interestingly, we found that the methylation level of several cytosines in the promoter CpG islands region of the predicted gene in gnp4 were different from the wild type. Thus, we propose that the DNA methylation changes at these sites may induce to decrease expression level of Gnp4, consequently, resulting in phenotypic variation.
Keywords:  rice      gnp4      lax1-1      grain number per-panicle      methylation  
Received: 02 September 2011   Accepted:
Fund: 

This work was funded by the Project of the 973 Program (2010CB125904), the 948 Program (2011-G2B), the National Natural Science Foundation of China (31171521) and the National Key Technology R&D Program of China (2009BADA2B01).

Corresponding Authors:  Correspondence LI Zi-chao, Tel: +86-10-62731414, E-mail: lizichao@cau.edu.cn     E-mail:  lizichao@cau.edu.cn

Cite this article: 

ZHANG Zhan-ying, LI Jin-jie, YAO Guo-xin, ZHANG Hong-liang, DOU Hui-jing, SHI Hong-li, SUN Xingming, LI Zi-chao. 2011. Fine Mapping and Cloning of the Grain Number Per-Panicle Gene (Gnp4) on Chromosome 4 in Rice (Oryza sativa L.). Journal of Integrative Agriculture, 10(12): 1825-1833.

[1]Ashikari M, Sakakibara H, Lin S Y, Yamamoto T, Takashi T, Nishimura A, Angeles E R, Qian Q, Kitano H , Matsuoka M. 2005. Cytokinin oxidase regulates rice grain production. Science, 309, 741-745.

[2]Goff S A, Ricke D, Lan T H, Presting G, Wang R L, Dunn M, Glazebrook J, Sessions A, Oeller P, Varma H. 2002. A draft sequence of the rice genome (Oryza sativa L. ssp. japonica). Science, 296, 92-100.

[3]Huang X, Qian Q, Liu Z, Sun H, He S, Luo D, Xia G, Chu C, Li J, Fu X. 2009. Natural variation at the DEP1 locus enhances grain yield in rice. Nature Genetics, 41, 494-497.

[4]Ikeda K, Ito M, Nagasawa N, Kyozuka J , Nagato Y. 2007, Rice aberrant panicle organization 1, encoding an F-box protein, regulates meristem fate. The Plant Journal, 51, 1030-1040.

[5]Kakutani T, Munakata K, Richards E J, Hirochika H. 1999. Meiotically and mitotically stable inheritance of DNA hypomethylation induced by ddm1 mutation of arabidopsis thaliana. Genetics, 151, 831-838.

[6]Kakutani T. 2002. Epi-alleles in plants: Inheritance of epigenetic information over generations. Plant Cell Physiology, 43, 1106-1111.

[7]Kinoshita Y, Saze H, Kinoshita T, Miura A, Soppe W J, Koornneef M, Kakutani T. 2007. Control of FWA gene silencing in Arabidopsis thaliana by SINE-related direct repeats. The Plant Journal, 49, 38-45.

[8]Komatsu K, Maekawa M, Ujiie S, Satake Y, Furutani I, Okamoto H, Shimamoto K, Kyozuka J. 2003. LAX and SPA: Major regulators of shoot branchingin rice. Proceedings of the National Academy of Sciences of the USA, 100, 11765-11770.

[9]Komatsu M, Atsushi C A, Nagato Y. 2003. FRIZZY PANICLE is required to prevent the formation of axillary meristemsand to establish floral meristem identity in rice spikelets. Development, 130, 3841-3850.

[10]Kurakawa T, Ueda N, Maekawa M, Kobayashi K, Kojima M, Nagato Y, Sakakibara H, Kyozuka J. 2007. Direct control of shoot meristem activity by a cytokinin-activating enzyme. Nature, 445, 652-655.

[11]Li F, Liu W, Tang J, Chen J, Tong H, Hu B, Li C, Fang J, Chen M, Chu C. 2010. Rice dense and erect panicle 2 is essential for determining panicle outgrowth and elongation. Cell Research, 20, 839-849.

[12]Li M, Tang D, Wang K J, Wu X R, Lu L L, Yu H X, Gu M H, Yan C J, Cheng Z K. 2011. Mutations in the F-box gene LARGER PANICLE improve the panicle architecture and enhance the grain yield in rice. Plant Biotechnology Journal, 10, 1467-7652.

[13]Li S B, Qian Q, Fu Z M, Zeng D L, Meng X B, Kyozuka J, M M, Zhu X D, Zhang J, Li J Y. 2009. Short panicle1 encodes a putative PTR family transporter and determines rice panicle size. The Plant Journal, 58, 592-605.

[14]Li X, Qian Q, Fu Z M, Wang Y H, Xiong G S, Zeng D L, Wang X Q, Liu X F, Teng S, Hiroshi F. 2003. Control of tillering in rice. Nature, 422, 618-621.

[15]Liu T M, Mao D H, Zhang S P, Xu C G, Xing Y Z. 2009. Fine mapping SPP1, a QTL controlling the number of spikelets per panicle, to a BAC clone in rice (Oryza sativa L.). Theoretical and Applied Genetics, 118, 1509-1517.

[16]Manning K, Tor1 M, Poole M, Hong Y G, Thompson A J, King G J, Giovannoni J J, Seymour G B. 2006. A naturally occurring epigenetic mutation in a gene encoding an SBP-box transcription factor inhibits tomato fruit ripening. Nature Genetics, 38, 948-952.

[17]Miura K, Ikeda M, Matsubara A, Song X J, Ito M, Asano K, Matsuoka M, Kitano H, Ashikari M. 2010. OsSPL14 promotes panicle branching and higher grain productivity in rice. Nature Genetics, 42, 545-549.

[18]Miura K, Agetsuma M, Kitano H, Yoshimura A, Matsuoka M, Jacobsen S E, Ashikari M. 2009. A metastable DWARF1 epigenetic mutant affecting plant stature in rice. Proceedings of the National Academy of Sciences of the USA, 106, 11218-11223.

[19]Oikawa T, Kyozuka J. 2009. Two-step regulation of LAX PANICLE1 protein accumulation in axillary meristem formation in rice. The Plant Cell, 21, 1095-1108.

[20]Panaud O, Chen X, McCouch S R. 1996. Development of microsatellite markers and characterization of simple sequence length polymorphism (SSLP) in rice (Oryza sativa L.). Molecular Genetics and Genomics, 252, 597-607.

[21]Qi F, Zhang Y J, Hao P, Wang S Y, Fu G, Huang Y C, Li Y, Zhu J J, Liu Y L, Hu X. 2002. Sequence and analysis of rice chromosome 4. Nature, 420, 316-321.

[22]Qiao Y L, Piao R H, Shi J X, Lee S I, Jiang W Z, Kim B K, Lee J, Han L Z, Ma W B, Koh H J. 2011. Fine mapping and candidate gene analysis of dense and erect panicle 3, DEP3, which confers high grain yield in rice (Oryza sativa L.). Theoretical and Applied Genetics, 122, 1439-1449.

[23]Sun F L, Zhang W P, Xiong G S, Yan M X,Qian Q, Li J Y, Wang Y H. 2011. Identification and functional analysis of the MOC1 interacting protein 1. Journal of Genetics and Genomics, 37, 69-77.

[24]Tian F, Zhu Z F, Zhang B S, Tan, L B, Fu Y C, Wang X K, Sun C Q. 2006. Fine mapping of a quantitative trait locus for grain number per panicle from wild rice (Oryza ruppogon Griff.). Theoretical and Applied Genetics, 113, 619-629.

[25]Wang J, Nakazaki T, Chen S, Chen W, Satio H, Tsukiyama T, Okumoto Y, Xu Z, Tanisaka T. 2009. Identification and characterization of the erect-pose panicle gene EP conferring high grain yield in rice (Oryza sativa L.). Theoretical and Applied Genetics, 119, 85-91.

[26]Xue W, Xing Y, Weng X, Zhao Y, Tang W, Wang L, Zhou H, Yu S, Xu C, Li X, Zhang Q. 2008. Natural variation in Ghd7 is an important regulator of heading date and yield potential in rice. Nature Genetics, 40, 761-767.

[27]Xing Y Z, Tang W J, Xue W Y, Xu CG, Zhang Q F. 2008. Four rice QTL controlling number of spikelets per panicle expressed the characteristics of single Mendelian gene in near isogenic backgrounds. Theoretical and Applied Genetics, 116, 789-796.

[28]Yan W H, Wang P, Chen X H, Zhou H J, Li Q P, Wang C R, Ding Z H, Zhang Y S, Yu S B, Xing Y Z. 2011. A major QTL, Ghd8, plays pleiotropic roles in regulating grain productivity, plant height, and heading date in rice. Molecular Plant, 4, 319-330.

[29]Yu J, Hu S N, Wang J, Wong G K, Li S G, Liu B, Deng Y J, Dai L, Zhou Y, Zhang X Q. 2002. A draft sequence of the rice genome (Oryza sativa L. ssp. indica). Science, 296, 79-92.

[30]Zhu K M, Tang D, Yan C J, Chi Z C, Yu H X, Chen J M, Liang J S, Gu M H, Cheng Z K. 2010. ERECT PANICAL2 encodes a novel protein that regulates panicle erectness in indica rice. Genetics, 184, 343-350.

[31]Zhou Y, Zhu J, Li Z, Yi C, Liu J, Zhang H, Tang S, Gu M, Liang G. 2009. Deletion in a quantitative trait gene qPE9-1 associated with panicle erectness improves plant architecture during rice domestication. Genetics, 183, 315-324.
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