Research Paper

Poaceae Orthologs of Rice OsSGL, DUF1645 Domain-Containing Genes, Positively Regulate Drought Tolerance, Grain Length and Weight in Rice

Expand
  • 1Key Laboratory of Agro-Ecological Processes in Subtropical Region, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125, China
    2University of the Chinese Academy of Sciences, Beijing 100049, China
    3College of Agriculture and Biotechnology, Hunan University of Humanities, Science and Technology, Loudi 417000, China
Wang Manling (mlwang@isa.ac.cn);
Cui Yanchun (cuiyanchun@isa.ac.cn)

Received date: 2021-06-03

  Accepted date: 2021-11-09

  Online published: 2022-03-10

Abstract

Grain yield is a polygenic trait that can be influenced by environmental factors and genetic compositions at all plant growth stages. Currently, the molecular mechanisms behind the coordination of the interaction between grain yield-related traits remain unknown. In this study, we characterized the function of four STRESS_tolerance and GRAIN_LENGTH (OsSGL) Poaceae ortholog genes that are transcribed into DUF1645 domain-containing proteins in relation to the grain length, grain weight, and drought stress-tolerance of rice. The transgenic plants with overexpressing or heterologous high levels of Poaceae OsSGL ortholog genes exhibited longer grain size than the wild type plants. Larger cells were seen in panicles of the four transgenic lines with paraffin sectioning and scanning electron microscopy analyses. In addition, four Poaceae OsSGL ortholog genes positively affected the drought tolerance of rice. Four transgenic plants displayed higher resistance to drought stress at the seedling and vegetative stages. RNA-sequencing and qRT-PCR results indicated that over- or heterologous-expression of four Poaceae OsSGL ortholog genes also affected the transcriptome of rice plants. These genes may play a role in auxin and cytokinin biosynthesis and their transduction pathways. Taken together, these results suggested that the four OsSGL orthologs have a conserved function in the regulation of stress-tolerance and cell growth by modulating hormonal biosynthesis and signaling.

Cite this article

Liu Kai, Li Minjuan, Zhang Bin, Yin Xuming, Xia Xinjie, Wang Manling, Cui Yanchun . Poaceae Orthologs of Rice OsSGL, DUF1645 Domain-Containing Genes, Positively Regulate Drought Tolerance, Grain Length and Weight in Rice[J]. Rice Science, 2022 , 29(3) : 257 -267 . DOI: 10.1016/j.rsci.2021.11.001

References

[1] Cao Y D, Xiao X Y, Ye N Z, Ding X W, Yi X X, Liu J L, Xiao Y H. 2021. Auxin regulator OsGRF4 simultaneously regulates rice grain shape and blast resistance. Chin J Rice Sci, 35(6): 629-638. (in Chinese with English abstract)
[2] Cui Y C, Wang M L, Zhou H N, Li M J, Huang L F, Yin X M, Zhao G Q, Lin F C, Xia X J, Xu G Y. 2016. OsSGL, a novel DUF1645 domain-containing protein, confers enhanced drought tolerance in transgenic rice and Arabidopsis. Front Plant Sci, 7: 2001.
[3] Fan C C, Xing Y Z, Mao H L, Lu T T, Han B, Xu C G, Li X H, Zhang Q F. 2006. 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, 112(6): 1164-1171.
[4] Guo C M, Luo C K, Guo L J, Li M, Guo X L, Zhang Y X, Wang L J, Chen L. 2016. OsSIDP366, a DUF1644 gene, positively regulates responses to drought and salt stresses in rice. J Integr Plant Biol, 58(5): 492-502.
[5] Hou X N, Liang Y Z, He X L, Shen Y Z, Huang Z J. 2013. A novel ABA-responsive TaSRHP gene from wheat contributes to enhanced resistance to salt stress in Arabidopsis thaliana. Plant Mol Biol Rep, 31(4): 791-801.
[6] Ishimaru K, Hirotsu N, Madoka Y, Murakami N, Hara N, Onodera H, Kashiwagi T, Ujiie K, Shimizu B I, Onishi A, Miyagawa H, Katoh E. 2013. Loss of function of the IAA-glucose hydrolase gene TGW6 enhances rice grain weight and increases yield. Nat Genet, 45(6): 707-711.
[7] Korver R A, Koevoets I T, Testerink C. 2018. Out of shape during stress: A key role for auxin. Trends Plant Sci, 23(9): 783-793.
[8] Kramer G F, Norman H A, Krizek D T, Mirecki R M. 1991. Influence of UV-B radiation on polyamines, lipid peroxidation and membrane lipids in cucumber. Phytochemistry, 30(7): 2101-2108.
[9] Li Q, Li L, Yang X H, Warburton M L, Bai G H, Dai J R, Li J S, Yan J B. 2010a. Relationship, evolutionary fate and function of two maize co-orthologs of rice GW2 associated with kernel size and weight. BMC Plant Biol, 10: 143.
[10] Li Q, Yang X H, Bai G H, Warburton M L, Mahuku G, Gore M, Dai J R, Li J S, Yan J B. 2010b. Cloning and characterization of a putative GS3 ortholog involved in maize kernel development. Theor Appl Genet, 120(4): 753-763.
[11] Li X J, Sun L J, Tan L B, Liu F X, Zhu Z F, Fu Y C, Sun X Y, Sun X W, Xie D X, Sun C Q. 2012. TH1, a DUF640 domain like gene controls lemma and palea development in rice. Plant Mol Biol, 78: 351-359.
[12] Liu J, Deng M, Guo H, Raihan S, Luo J Y, Xu Y C, Dong X F, Yan J B. 2015. Maize orthologs of rice GS5 and their trans-regulator are associated with kernel development. J Integr Plant Biol, 57(11): 943-953.
[13] Liu J L, Moore S, Chen C L, Lindsey K. 2017. Crosstalk complexities between auxin, cytokinin, and ethylene in Arabidopsis root development: From experiments to systems modeling, and back again. Mol Plant, 10(12): 1480-1496.
[14] Liu L C, Tong H N, Xiao Y H, Che R H, Xu F, Hu B, Liang C Z, Chu J F, Li J Y, Chu C C. 2015. Activation of Big Grain1 significantly improves grain size by regulating auxin transport in rice. Proc Natl Acad Sci USA, 112(35): 11102-11107.
[15] Ma L, Li T, Hao C Y, Wang Y Q, Chen X H, Zhang X Y. 2016. TaGS5-3A, a grain size gene selected during wheat improvement for larger kernel and yield. Plant Biotechnol J, 14(5): 1269-1280.
[16] Maier M A, Uchii K, Peterson T D, Kagami M. 2016. Evaluation of daphnid grazing on microscopic zoosporic fungi by using comparative threshold cycle quantitative PCR. Appl Environ Microbiol, 82(13): 3868-3874.
[17] Mao H L, Sun S Y, Yao J L, Wang C R, Yu S B, Xu C G, Li X H, Zhang Q F. 2010. Linking differential domain functions of the GS3 protein to natural variation of grain size in rice. Proc Natl Acad Sci USA, 107(45): 19579-19584.
[18] Morris D L. 1948. Quantitative determination of carbohydrates with dreywood’s anthrone reagent. Science, 107: 254-255.
[19] Mustafiz A, Kumari S, Karan R. 2016. Ascribing functions to genes: Journey towards genetic improvement of rice via functional genomics. Curr Genomics, 17(3): 155-176.
[20] Panda D, Sakambari M S, Kumar B P. 2021. Drought tolerance in rice: Focus on recent mechanisms and approaches. Rice Sci, 28(2): 119-132.
[21] Pardo J M. 2010. Biotechnology of water and salinity stress tolerance. Curr Opin Biotechnol, 21(2): 185-196.
[22] Qin L, Zhao J J, Li T, Hou J, Zhang X Y, Hao C Y. 2017. TaGW2, a good reflection of wheat polyploidization and evolution. Front Plant Sci, 8: 318.
[23] Ren D Y, Rao Y C, Wu L W, Xu Q K, Li Z Z, Yu H P, Zhang Y, Leng Y J, Hu J, Zhu L, Gao Z Y, Dong G J, Zhang G H, Guo L B, Zeng D L, Qian Q. 2016. The pleiotropic ABNORMAL FLOWER AND DWARF1 affects plant height, floral development and grain yield in rice. J Integr Plant Biol, 58(6): 529-539.
[24] Sawano Y, Miyakawa T, Yamazaki H, Tanokura M, Hatano K I. 2007. Purification, characterization, and molecular gene cloning of an antifungal protein from Ginkgo biloba seeds. Biol Chem, 388(3): 273-280.
[25] Scheres B, van der Putten W H. 2017. The plant perceptron connects environment to development. Nature, 543: 337-345.
[26] Seo Y S, Chern M, Bartley L E, Han M, Jung K H, Lee I, Walia H, Richter T, Xu X, Cao P J, Bai W, Ramanan R, Amonpant F, Arul L, Canlas P E, Ruan R, Park C J, Chen X W, Hwang S, Jeon J S, Ronald P C. 2011. Towards establishment of a rice stress response interactome. PLoS Genet, 7(4): e1002020.
[27] Simmonds J, Scott P, Brinton J, Mestre T C, Bush M, del Blanco A, Dubcovsky J, Uauy C. 2016. A splice acceptor site mutation in TaGW2-A1 increases thousand grain weight in tetraploid and hexaploid wheat through wider and longer grains. Theor Appl Genet, 129(6): 1099-1112.
[28] Song X J, Huang W, Shi M, Zhu M Z, Lin H X. 2007. A QTL for rice grain width and weight encodes a previously unknown RING-type E3 ubiquitin ligase. Nat Genet, 39(5): 623-630.
[29] Su Z Q, Hao C Y, Wang L F, Dong Y C, Zhang X Y. 2011. Identification and development of a functional marker of TaGW2 associated with grain weight in bread wheat (Triticum aestivum L.). Theor Appl Genet, 122(1): 211-223.
[30] Troll W, Lindsley J. 1955. A photometric method for the determination of proline. J Biol Chem, 215(2): 655-660.
[31] Valluru R, Reynolds M P, Salse J. 2014. Genetic and molecular bases of yield-associated traits: A translational biology approach between rice and wheat. Theor Appl Genet, 127(7): 1463-1489.
[32] Wang M L, Lu X D, Xu G Y, Yin X M, Cui Y C, Huang L F, Rocha P S C F, Xia X J. 2016. OsSGL, a novel pleiotropic stress-related gene enhances grain length and yield in rice. Sci Rep, 6(1): 38157.
[33] Wang S S, Zhang X F, Chen F, Cui D Q. 2015. A single-nucleotide polymorphism of TaGS5 gene revealed its association with kernel weight in Chinese bread wheat. Front Plant Sci, 6: 1166.
[34] Wing R A, Purugganan M D, Zhang Q F. 2018. The rice genome revolution: From an ancient grain to green super rice. Nat Rev Genet, 19(8): 505-517.
[35] Xu C J, Liu Y, Li Y B, Xu X D, Xu C G, Li X H, Xiao J H, Zhang Q F. 2015. Differential expression of GS5 regulates grain size in rice. J Exp Bot, 66(9): 2611-2623.
[36] Yoshida A, Suzaki T, Tanaka W, Hirano H Y. 2009. The homeotic gene long sterile lemma (G1) specifies sterile lemma identity in the rice spikelet. Proc Natl Acad Sci USA, 106(47): 20103-20108.
[37] Zhang B, Zhang X, Xu G Y, Li M J, Cui Y C, Yin X M, Yu Y, Xia X J, Wang M L. 2018. Expression of sorghum gene SbSGL enhances grain length and weight in rice. Mol Breeding, 38(4): 40.
[38] Zhang L, Tian L H, Zhao J F, Song Y, Zhang C J, Guo Y. 2009. Identification of an apoplastic protein involved in the initial phase of salt stress response in rice root by two-dimensional electrophoresis. Plant Physiol, 149(2): 916-928.
[39] Zhou C H, Zhao Z K, Pan X H, Huang S, Tan X M, Wu J F, Shi Q H. 2016. Integration of growing milk vetch in winter and reducing nitrogen fertilizer application can improve rice yield in double-rice cropping system. Rice Sci, 23(3): 132-143.
[40] Zhou T S, Yu D, Liu L, Ouyang N, Yuan G L, Duan M J, Yuan D Y. 2021. CRISPR/Cas9-mediated editing of AFP1 improves rice stress tolerance. Chin J Rice Sci, 35(1): 11-18. (in Chinese with English abstract)
[41] Zuo J R, Li J Y. 2014. Molecular dissection of complex agronomic traits of rice: A team effort by Chinese scientists in recent years. Natl Sci Rev, 1(2): 253-276.
Outlines

/

浙ICP备05004719号-15   公安备案号:33010302003355
Copyright © Editorial office of Rice Science
Tel: 0571-63371017 E-mail: crrn@fy.hz.zn.cn; cjrs278@gmail.com
Supported by Beijing Magtech Co., Ltd.
Total visitors:  Visitors of today:  Now online: