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Ghd7, a pleiotropic gene controlling flag leaf area in rice

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  • National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, China

Received date: 2012-02-09

  Revised date: 2012-04-06

  Online published: 2012-07-25

Abstract

Photosynthesis is the unique source of energy for plant. Flag leaf contributed the majority of photosynthate after rice flowering. Ghd7 is a pleiotropic gene, which can significantly increase rice production. In order to study the genetic effects of Ghd7 on the flag leaf morphology, we made quantitative trait locus (QTL) analysis for flag leaf length (FLL), flag leaf width (FLW), and flag leaf area (FLA) using a Ghd7-BC2F2 popu-lation of 190 plants. In the BC2F2 population, the frequency distribution of FLL, FLW, and FLA were bimodal and in agreement with single Mendelian segregation ratio (3:1). FLL, FLW, and FLA were positively correlated with grains per panicle in the population. One QTL was mapped to the interval between markers RM3859 and C39 on chromosome 7, which explained 73.3%, 62.3%, and 71.8% of the variations for FLL, FLW, and FLA, and co-segregated with Ghd7. Two near-isogenic lines of NIL (mh7) and NIL (tq7) were developed using Zhenshan 97 as the recurrent parent and Minghui 63 and Teqing as the donor parent, respectively. Both NILs significantly increased the phenotypic values of FLL, FLW, and FLA as compared with Zhenshan 97. FLL, The values of FLW and FLA for Ghd7 over-expression transgenic plants were 8.9 cm, 0.5 cm, and 17.8 cm2 larger than its recipient Hejiang 19. These results demonstrated that Ghd7 plays an important role in controlling the flag leaf area in rice.

Cite this article

TAN Cong, WENG Xiao-Yu, YAN Wen-Hao, BAI Xu-Feng, XING Yong-Zhong . Ghd7, a pleiotropic gene controlling flag leaf area in rice[J]. Hereditas(Beijing), 2012 , 34(7) : 901 -906 . DOI: 10.3724/SP.J.1005.2012.00901

References

[1] Gladun IV, Karpov EA. Distribution of assimilates from the flag leaf of rice during the reproductive period of development. Russ J Plant Physiol, 1993, 40(1): 215-219.
[2] Yonezawa K. Yield components. In: Science of the Rice Plant vol. III Genetics. Tokyo, Japan, 1997: 400-412.
[3] Yue B, Xue WY, Luo LJ, Xing YZ. QTL analysis for flag leaf characteristics and their relationships with yield and yield traits in rice. Acta Genet Sin, 2006, 33(9): 824-832.
[4] Yan JP, Zhu J, He CX, Benmoussa M, Wu P. Molecular marker-assisted dissection of genotype× environment interaction for plant type traits in rice (Oryza sa-tiva L.). Crop Sci, 1999, 39(2): 538-544.
[5] Kobayashi S, Fukuta Y, Morita S, Sato T, Osaki M, Khush GS. Quantitative trait loci affecting flag leaf development in rice (Oryza sativa L.). Breed Sci, 2003, 53(3): 255-262.
[6] Mei HW, Li ZK, Shu QY, Guo LB, Wang YP, Yu XQ, Ying CS, Luo LJ. Gene actions of QTLs affecting several agronomic traits resolved in a recombinant inbred rice population and two backcross populations. Theor Appl Genet, 2005, 110(4):649-659.
[7] Yoon DB, Kang KH, Kim HJ, Ju HG, Kwon SJ, Suh JP, Jeong OY, Ahn SN. Mapping quantitative trait loci for yield components and morphological traits in an advanced backcross population between Oryza grandiglumis and the O.sativa japonica cultivar Hwaseongbyeo. Theor Appl Genet, 2006, 112(6): 1052-1062.
[8] Zhang Y, Wang J, Xu C, Xing Y. Molecular dissection of genetic basis of significant correlation among five morphological traits in rice. Chin Sci Bull, 2010, 55(27): 3154-3160.
[9] Thomson MJ, Tai TH, McClung AM, Lai XH, Hinga ME, Lobos KB, Xu Y, Martinez CP, McCouch SR. Mapping quantitative trait loci for yield, yield components and morphological traits in an advanced backcross population between Oryza rufipogon and the Oryza sativa cultivar Jefferson. Theor Appl Genet, 2003, 107(3): 479-493.
[10] Jiang S, Zhang X, Wang J, Chen W, Xu Z. Fine mapping of the quantitative trait locus qFLL9 controlling flag leaf length in rice. Euphytica, 2010, 176(3): 341-347.
[11] Wang, P, Zhou GL, Yu HH, Yu SB. Fine mapping a major QTL for flag leaf size and yield-related traits in rice. Theor Appl Genet, 2011, 123(8): 1319-1330.
[12] Price AH. Believe it or not, QTLs are accurate! Trends Plant Sci, 2006, 11(5): 213-216.
[13] Fan C, Xing Y, Mao H, Lu T, Han B, Xu C, Li X, Zhang Q. GS3, a major QTL for grain length and weight and minor QTL for grain width and thickness in rice, encodes a putative transmembrane protein. Theor Appl Genet, 2006, 112(6): 1164-1171.
[14] Li Y, Fan C, Xing Y, Jiang Y, Luo L, Sun L, Shao D, Xu C, Li X, Xiao J, He Y, Zhang Q. Natural variation in GS5 plays an important role in regulating grain size and yield in rice. Nat Genet, 2011, 43(12): 1266-1269.
[15] Song XJ, Huang W, Shi M, Zhu MZ, Lin HX. A QTL for rice grain width and weight encodes a previously unknown RING-type E3 ubiquitin ligase. Nat Genet, 2007, 39(5): 623-630.
[16] Weng J, Gu S, Wan X, Gao H, Guo T, Su N, Lei C, Zhang X, Cheng Z, Guo X, Wang J, Jiang L, Zhai H, Wan J. Isolation and initial characterization of GW5, a major QTL associated with rice grain width and weight. Cell Res, 2008, 18(12): 1199-1209.
[17] Ashikari M, Sakakibara H, Lin S, Yamamoto T, Takashi T, Nishimura A, Angeles ER, Qian Q, Kitano H, Matsuoka M. Cytokinin oxidase regulates rice grain production. Science, 2005, 309(5735): 741-745.
[18] Xue W, Xing Y, Weng X, Zhao Y, Tang W, Wang L, Zhou H, Yu S, Xu C, Li X, Zhang Q. Natural variation in Ghd7 is an important regulator of heading date and yield potential in rice. Nat Genet, 2008, 40(6): 761-767.
[19] Yan WH, Wang P, Chen HX, Zhou HJ, Li QP, Wang CR, Ding ZH,
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