
Chinese Journal OF Rice Science >
Cytological Observation of a Female and Male Sterile Osfma2 Mutant in Rice and Its Map-based Cloning
#These authors contributed equally to this work;
Received date: 2021-03-23
Revised date: 2021-04-22
Online published: 2022-01-10
【Objective】 The work aims to locate and clone the rice female and male sterile gene OsFMA2 by constructing a segregated population and explore its function in the regulation of rice fertility. 【Method】 Stable sterile mutants were obtained by EMS mutagenesis of japonica rice Ningjing 4, and the phenotypic and cytological observation of the mutant was conducted. Using map-based cloning and Mut-map methods, the female and male sterile gene OsFMA2 was fine-mapped and cloned. The expression pattern of OsFMA2 in various tissues was analyzed by the real-time quantitative PCR technique. Subcellular localization of OsFMA2 protein was performed with the rice protoplast expression system. 【Result】 The cytological observation revealed that the Osfma2 mutant was male- and female-sterile, and the extreme individuals were used to locate the gene in a 448-kb interval on the long arm of chromosome 6. The gene OsFMA2 is predicted to encode a replication protein that is highly conserved in monocots. The gene OsFMA2 was tissue-specific and was highly expressed in young panicles. Subcellular localization analysis showed that the OsFMA2 protein was localized on the nucleus. 【Conclusion】The gene OsFMA2 is highly expressed in young panicles, and it may participate in the homologous recombination of the first meiotic division of male gamete. At the same time, the expression of OsFMA2 also has an adverse effect on the development of female gametes.
ZHANG Taohui, WANG Haiyu, WAN Hua, ZHANG Liping, XIE Zhenwei, CHEN Keyi, HE Xiaodong, ZHAO Zhigang, WAN Jianmin . Cytological Observation of a Female and Male Sterile Osfma2 Mutant in Rice and Its Map-based Cloning[J]. Chinese Journal OF Rice Science, 2022 , 36(1) : 13 -26 . DOI: 10.16819/j.1001-7216.2022.210312
| [1] | 谭何新, 文铁桥, 张大兵. 水稻花粉发育的分子机理[J]. 植物学通报, 2007,24(3):330-339. |
| [1] | Tan H X, Wen T Q, Zhang D B. Molecular mechanisms of pollen development in Oryza sativa[J]. Chinese Bulletin of Botany, 2007,24(3):330-339. (in Chinese with English abstract) |
| [2] | 马西青, 方才臣, 邓联武, 万向元. 水稻隐性核雄性不育基因研究进展及育种应用探讨[J]. 中国水稻科学, 2012,26(5):511-520. |
| [2] | Wan X Q, Fang C C, Deng L W, Wan X Y. Research progress and breeding application of recessive genic male sterility genes in rice[J]. Chinese Journal of Rice Science, 2012,26(5):511-520. (in Chinese with English abstract) |
| [3] | 官文祥, 邓赟, 李小旭, 吴为人, 郑燕. 水稻雌性不育分子机理研究进展[J]. 分子植物育种, 2017,15(2):672-684. |
| [3] | Guan W X, Deng Y, Li X X, Wu W R, Zheng Y. Advances in research on molecular mechanism of female sterility in rice (Oryza sativa L.)[J]. Molecular Plant Breeding, 2017,15(2):672-684. (in Chinese with English abstract) |
| [4] | 刘春宏, 方珊茹, 刘玉芹, 沈伟锋. 水稻雄性核不育基因的研究进展[J]. 台湾农业探索, 2012,19(1):71-75. |
| [4] | Liu C H, Fang S R, Liu Y Q, Shen W F. Research progress on genic male sterile genes in rice (Oryza sativa L)[J]. Taiwan Agricultural Research, 2012,19(1):71-75. (in Chinese with English abstract) |
| [5] | Wang C, Liu Q, Shen Y, Hua Y, Wang J J, Lin J R, Wu M G, Sun T T, Cheng Z K, Mercier R. Clonal seeds from hybrid rice by simultaneous genome engineering of meiosis and fertilization genes[J]. Nature Biotechnology, 2019,37(3):283-286. |
| [6] | Nonomur K, Nakano M, Fukuda T, Eiguchi M, Miyao A, Hirochika H, Kurata N. The novel gene HOMOLOGOUS PAIRING ABERRATION IN RICE MEIOSIS1 of rice encodes a putative coiled-coil protein required for homologous chromosome pairing in meiosis[J]. The Plant Cell, 2004,16(4):1008-1020. |
| [7] | Chang L, Ma H, Xue H W. Functional conservation of the meiotic genes SDS and RCK in male meiosis in the monocot rice[J]. Cell Research, 2009,19(6):768-782. |
| [8] | Yu H X, Wang M, Tang D, Wang K J, Chen F L, Gong Z Y, Gu M H, Cheng Z K. OsSPO11-1 is essential for both homologous chromosome pairing and crossover formation in rice[J]. Chromosoma, 2010,119(6):625-636. |
| [9] | Wang Y X, Copenhaver G. Meiotic recombination: mixing it up in plants[J]. Annual Review of Plant Biology, 2018,69(1):577-609. |
| [10] | Shingu Y, Tokai T, Agawa Y, Toyota K, Ahmed S, Kobayashi M, Komatsu A, Mikawa T, Yamamoto M, Wakasa K, Shibata T, Kusano K. The double-stranded break-forming activity of plant SPO11s and a novel rice SPO11 revealed by a Drosophila bioassay[J]. BMC Molecular Biology, 2012,13:1-16. |
| [11] | Zhang B W, Wang M, Tang D, Li Y F, Xu M, Gu M H, Cheng Z K, Yu H X. XRCC3 is essential for proper double-strand break repair and homologous recombination in rice meiosis[J]. Journal of Experimental Botany, 2015,66(19):5713-5725. |
| [12] | Deng Z Y, Wang T. OsDMC1 is required for homologous pairing in Oryza sativa[J]. Plant Molecular Biology, 2007,65(1-2):31-42. |
| [13] | Sheridan S, Yu X, Roth R, Heuser J, Sehorn M, Sung P, Egelman E, Bishop D. A comparative analysis of Dmc1 and Rad51 nucleoprotein filaments[J]. Nucleic Acids Research, 2008,36(12):4057-4066. |
| [14] | Sakane I, Kamataki C, Takizawa Y, Nakashima M, Toki S, Ichikawa H, Ikawa S, Shibata T, Kurumizaka H. Filament formation and robust strand exchange activities of the rice DMC1A and DMC1B proteins[J]. Nucleic Acids Research, 2008,36(13):4266-4276. |
| [15] | Morozumi Y, Ino R, Ikawa S, Mimida N, Shimizu T, Toki S, Ichikawa H, Shibata T, Kurumizaka H. Homologous pairing activities of two rice RAD51 proteins, RAD51A1 and RAD51A2[J]. PloS ONE, 2013,8(10):e75451. |
| [16] | Vries S, Baart E, Dekker M, Siezen A, Rooij D, Boer P, Riele H. Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis[J]. Gene & Development, 1999,13(5):523-531. |
| [17] | Mimitou E, Symington L. DNA end resection: Many nucleases make light work[J]. DNA Repair, 2009,8(9):983-995. |
| [18] | Youds J, Boulton S. The choice in meiosis defining the factors that influence crossover or non-crossover formation[J]. Journal of Cell Science, 2011,124(4):501-513. |
| [19] | Fairman M, Stillman B. Cellular factors required for multiple stages of SV40 DNA-replication in vitro[J]. The EMBO Journal, 1988,7(4):1211-1218. |
| [20] | Iftode C, Daniely Y, Borowiec J. Replication Protein A (RPA): The Eukaryotic SSB[J]. Critical Reviews in Biochemistry and Molecular Biology, 1999,34(3):141-180. |
| [21] | Osman K, Sanchez-Moran E, Mann S, Jones G, Franklin F. Replication protein A (AtRPA1a) is required for class I crossover formation but is dispensable for meiotic DNA break repair[J]. The EMBO Journal, 2009,28(4):394-404. |
| [22] | Takashi Y, Kobayashi Y, Tanaka K, Tamura K. Arabidopsis replication protein A 70a is required for DNA damage response and telomere length homeostasis[J]. Plant Cell Physiology, 2009,50(11):1965-1976. |
| [23] | Aklilu B, Soderquist R, Culligan K. Genetic analysis of the replication protein A large subunit family in Arabidopsis reveals unique and overlapping roles in DNA repair, meiosis and DNA replication[J]. Nucleic Acids Research, 2014,42(5):3104-3118. |
| [24] | Chang Y X, Gong L, Yuan W Y, Li X W, Chen G X, Li X H, Zhang Q F, Wu C Y. Replication Protein A (RPA1a) is required for meiotic and somatic DNA repair but is dispensable for DNA replication and homologous recombination in rice[J]. Plant Physiology, 2009,151(4):2162-2173. |
| [25] | Li X W, Chang Y X, Xin X D, Zhu C M, Li X H, Higgins J, Wu C Y. Replication protein A2c coupled with replication protein A1c regulates crossover formation during meiosis in rice[J]. The Plant Cell, 2013,25(10):3885-3899. |
| [26] | 冯九焕, 卢永根, 刘向东, 徐雪宾. 水稻花粉发育过程及其分期[J]. 中国水稻科学, 2001,15(1):22-29. |
| [26] | Feng J H, Lu Y G, Liu X D, Xu X B. Pollen development and its stages in rice (Oryza sativa L.)[J]. Chinese Journal of Rice Science, 2001,15(1):22-29. (in Chinese with English abstract) |
| [27] | Zhang D B, Luo X, Zhu L. Cytological analysis and genetic control of rice anther development[J]. Journal of Genetics and Genomics, 2011,38(9):379-390. |
| [28] | Xia R, Wang J G, Liu C Y, Wang Y Q, Zhai J X, Liu J, Hong X H, Cao X F, Zhu J K, Gong Z Z. ROR1/RPA2A, a putative replication protein A2, functions in epigenetic gene silencing and in regulation of meristem development in Arabidopsis[J]. The Plant Cell, 2006,18(1):85-103. |
| [29] | Belanger K, Griffith A, Baker H, Hansen J, Kovacs L, Seconi J, Strine A. The karyopherin Kap95 and the C-termini of Rfa1, Rfa2, and Rfa3 are necessary for efficient nuclear import of functional RPA complex proteins in Saccharomyces cerevisiae[J]. DNA and Cell Biology, 2011,30(9):641-651. |
| [30] | Keshav K F, Chen C, Dutta A. Rpa4, a homolog of the 34-kilodalton subunit of the replication protein A complex[J]. Molecular and Cellular Biology, 1995,15(6):3119-3128. |
| [31] | Zhang J, Han F P. Centromere pairing precedes meiotic chromosome pairing in plants[J]. Science China Life Sciences, 2017,60(11):1197-1202. |
| [32] | Simonet J, Zick D. Genes involved in caryogamy and meiosis in Podospora anserine[J]. Molecular Genetics Genomics, 1978,162(3):237-242. |
| [33] | Abe A, Kosugi S, Yoshida K, Natsume S, Takagi H, Matsumura H, Yoshida K, Mitsuoka C, Tamiru M. Genome sequencing reveals agronomically important loci in rice using MutMap[J]. Nature Biotechnology, 30(2):174-178. |
| [34] | Ishibashi T, Kimura S, Sakaguchi K. A higher plant has three different types of RPA heterotrimeric complex[J]. Journal of Biochemistry, 2006,139(1):99-104. |
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