水稻已克隆中胚轴伸长基因效应解析及优异单倍型鉴定

doi:10.11924/j.issn.1000-6850.casb2023-0286

中国农学通报 ›› 2024, Vol. 40 ›› Issue (12): 104-112.doi: 10.11924/j.issn.1000-6850.casb2023-0286

所属专题：水稻

水稻已克隆中胚轴伸长基因效应解析及优异单倍型鉴定

刘金栋¹^,²(), 王雅美²^,³, 田媛媛¹, 刘宏岩⁴, 孟云²^,⁴, 叶国友²^,⁵()

¹ 中国农业科学院作物科学研究所，北京 100081
² 中国农业科学院深圳农业基因组研究所，中国农业科学院-国际水稻研究所基因组学辅助种质改良联合实验室，深圳 518120
³ 中山大学农学院，深圳 518107
⁴ 海南大学三亚南繁研究院，海南三亚 572025
⁵ 国际水稻研究所，菲律宾马尼拉 090012

收稿日期:2023-03-18 修回日期:2023-04-25 出版日期:2024-04-25 发布日期:2024-04-22
通讯作者:
叶国友，男，1964年出生，河北张家口人，高级科学家，博士，研究方向：水稻复杂性状遗传机制解析。通信地址：518000 深圳市大鹏新区布新路97号，Tel：0755-23250158，E-mail：G.Ye@irri.org。
作者简介:
刘金栋，男，1990年出生，山东济宁人，副研究员，博士，研究方向：作物复杂性状遗传机制解析。通信地址：100081 北京市海淀区中关村南大街12号中国农业科学院，Tel：010-82108889，E-mail：liujindong@caas.cn。
基金资助:
中国科学技术协会青年人才托举工程(2020QNRC001); 广东省自然科学基金面上项目(2023A1515012040); 中国博士后科学基金面上项目(2022M723659); 广东省基础与应用基础研究基金项目(2022A1515111057)

The Cloned Genes Related to Rice Mesocotyl Elongation: Effects Analysis and Superior Haplotype Identification

LIU Jindong¹^,²(), WANG Yamei²^,³, TIAN Yuanyuan¹, LIU Hongyan⁴, MENG Yun²^,⁴, YE Guoyou²^,⁵()

¹ Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081
² Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518120
³ School of Agriculture, Sun Yat-sen University, Shenzhen 518107
⁴ Sanya Institute of Breeding and Multiplication, Hainan University, Sanya, Hainan 572025
⁵ International Rice Research Institute, Metro Manila, Philippines 090012

Received:2023-03-18 Revised:2023-04-25 Published:2024-04-25 Online:2024-04-22

摘要/Abstract

摘要：

旱直播是未来水稻生产的重要发展方向，在南亚和东南亚籼稻种植区已有较大面积，然而热带和亚热带地区粳稻种植多采用传统育苗移栽。中胚轴长度(Mesocotyl length，ML)是影响水稻旱直播出苗和幼苗活力的重要因素。基于分子标记辅助选择(Molecular marker assisted selection，MAS)育种，培育长中胚轴种质是促进水稻旱直播推广最为经济、高效的方式。迄今，已有4个水稻中胚轴伸长基因报道，即OsGSK2、GY1、OsPAO5和OsSMAX1。笔者选择3K重测序项目中TROP和TEMP粳稻亚群开展分析，测定中胚轴长度并鉴定OsGSK2、GY1、OsPAO5和OsSMAX1基因的优异单倍型。结果表明，TROP和TEMP亚群中胚轴长度呈典型的连续正态分布。OsGSK2、GY1、OsPAO5和OsSMAX1分别包括3、3、3和6种单倍型；同一基因在TROP和TEMP亚群中单倍型分布频率也存在差异。TROP亚群中OsGSK2-Hap1、GY1-Hap2、OsPAO5-Hap3、OsSMAX1-Hap2和OsSMAX1-Hap3为优异单倍型；TEMP亚群优异单倍型为OsGSK2-Hap1、OsPAO5-Hap2和OsSMAX1-Hap2。另外，TROP和TEMP亚群中多数中胚轴优异单倍型材料所对应的苗高要高于非优异单倍型，在破土出苗时易形成生长优势。鉴定到的优异单倍型在TROP和TEMP亚群中均呈现较显著的加性效应，可用于MAS育种。本研究为不同地区直播粳稻的选育提供参考，促进旱直播技术的快速推广。

关键词: 单倍型, 中胚轴长度, 水稻, 优异单倍型

Abstract:

Dry direct seeding is an important future direction of rice production with a large area in South Asia and Southeast Asia of Indica rice growing regions. However, Japonica rice planting in tropical and subtropical areas mostly adopts traditional transplanting method. Mesocotyl length (ML) is an important factor affecting the emergence and vigor of rice seedlings in dry direct seeding. Breeding long mesocotyl germplasm based on molecular marker assisted selection (MAS) is the most economical and efficient way to promote the popularization of rice direct seeding. So far, four rice mesocotyl elongation genes have been cloned and reported, namely OsGSK2, GY1, OsPAO5 and OsSMAX1, respectively. In this study, we selected the TROP and TEMP Japonica rice subpopulations originated from the 3K re-sequencing project for analysis, determined the length of mesocotyl and identified superior haplotypes of OsGSK2, GY1, OsPAO5 and OsSMAX1. The results showed that the ML of TROP and TEMP populations presented a typical continuous normal distribution. OsGSK2, GY1, OsPAO5 and OsSMAX1 include 3, 3, 3 and 6 haplotypes, respectively. The frequency of haplotype distribution was different in TROP and TEMP panels for the same gene. OsGSK2-Hap1, GY1-Hap2, OsPAO5-Hap3, OsSMAx1-Hap2 and OsSMAx-Hap3 were identified as superior genes in TROP panel; whereas superior haplotypes OsGSK2-Hap1, OsPAO5-Hap2 and OsSMAX1-Hap2 were identified in TEMP panel. In addition, the seedling height for superior haplotype accessions was higher than that of un-superior haplotype accessions in the TROP and TEMP panels, which was easy to form a growth advantage in growth. The superior haplotypes identified showed significant additive effects in TROP and TEMP panels, which could be used in MAS breeding. This study provides reference for the breeding of direct seeding Japonica rice in different regions, and promotes the rapid popularization of dry direct seeding technology.

Key words: haplotypes, mesocotyl length, rice, superior haplotypes

刘金栋, 王雅美, 田媛媛, 刘宏岩, 孟云, 叶国友. 水稻已克隆中胚轴伸长基因效应解析及优异单倍型鉴定[J]. 中国农学通报, 2024, 40(12): 104-112.

LIU Jindong, WANG Yamei, TIAN Yuanyuan, LIU Hongyan, MENG Yun, YE Guoyou. The Cloned Genes Related to Rice Mesocotyl Elongation: Effects Analysis and Superior Haplotype Identification[J]. Chinese Agricultural Science Bulletin, 2024, 40(12): 104-112.

图/表 6

参考文献 37

[1]	CHUNG N J. Elongation habit of mesocotyls and coleoptiles in weedy rice with high emergence ability in direct-seeding on dry paddy fields[J]. Crop & pasture science, 2010, 61:911-917.
[2]	WANG Y, LIU J, MENG Y, et al. Rapid identification of QTL for mesocotyl length in rice through combining QTL-seq and genome-wide association analysis[J/OL]. Frontiers in genetics, 2021, 12, https://doi.org/10.3389/fgene.2021.713446.
[3]	LIU H, ZHAN J, LI J, et al. Genome-wide association study (GWAS) for mesocotyl elongation in rice (Oryza sativa L.) under multiple culture conditions[J]. Genes, 2020, 11:49. doi: 10.3390/genes11010049 URL
[4]	ZHAN J, LU X, LIU H, et al. Mesocotyl elongation, an essential trait for dry-seeded rice (Oryza sativa L.): a review of physiological and genetic basis[J]. Planta, 2020, 251(1):1-14. doi: 10.1007/s00425-019-03297-x
[5]	TURNER F T, CHEN C C, BOLLICH C N. Coleoptile and mesocotyl lengths in semidwarf rice seedlings[J]. Crop science, 1982, 22:43-46. doi: 10.2135/cropsci1982.0011183X002200010010x URL
[6]	曹立勇, 朱军, 颜启传, 等. 水稻籼粳交DH群体幼苗中胚轴长度的QTLs定位和上位性分析[J]. 中国水稻科学, 2002, 3:24-27.
[7]	张光恒, 林建荣, 吴明国, 等. 水稻出苗顶土动力源研究[J]. 中国水稻科学, 2005, 19(1):59-62.
[8]	LEE H S, SASAKI K, KANG J, et al. Mesocotyl elongation is essential for seedling emergence under deep-seeding condition in rice[J]. Rice, 2017, 10(1):32. doi: 10.1186/s12284-017-0173-2 URL
[9]	WU M, ZHANG G, LIN J, et al. Screening for rice germplasms with specially elongated mesocotyl[J]. Rice science, 2005, 12:226-228.
[10]	MAHENDER A, ANANDAN A, PRADHAN S K. Early seedling vigor, an imperative trait for direct-seeded rice: an overview on physio-morphological parameters and molecular markers[J]. Planta 2015, 241:1027-1050. doi: 10.1007/s00425-015-2273-9 URL
[11]	KUMAR V, LADHA J K. Direct seeding of rice: recent developments and future research needs[J]. Advance in agronomy, 2011, 111:297-413.
[12]	刘畅, 孟云, 刘金栋, 等. 结合QTL-seq和连锁分析发掘水稻中胚轴伸长相关QTL[J]. 作物学报, 2021, 47(10):2036-2044. doi: 10.3724/SP.J.1006.2021.02082
[13]	GRAY W M, OSTIN A, SANDBERG G, et al. High temperature promotes auxin-mediated hypocotyl elongation in Arabidopsis[J]. Proceedings of the national academy of sciences of the United States of America, 1998, 95(12):7197-7202.
[14]	KATO Y, KATSURA K. Rice adaptation to aerobic soils: physiological considerations and implications for agronomy[J]. Plant production science, 2014, 17:1-12. doi: 10.1626/pps.17.1 URL
[15]	XU Z H, XUE H W. Plant hormones: function and molecular mechanism[M]. Shanghai Scientific and Technical Publishers, Shanghai, 2012:45-67.
[16]	WU S Q, DING R, LI X S. Regulation of mesocotyl growth by gibberellic acid and abscisic acid in etiolated seedlings of black rice[J]. Amino acids and biotic resources, 2002, 24:44-45.
[17]	ZHAO G, FU J, WANG G, et al. Gibberellin-induced mesocotyl elongation in deep-sowing tolerant maize inbred line[J]. Plant breeding, 2010, 129(1):87-91. doi: 10.1111/pbr.2010.129.issue-1 URL
[18]	LIANG Q, WANG C, MA D R, et al. Cortical microtubule disorganized related to an endogenous gibberellin increase plays an important role in rice mesocotyl elongation[J]. Plant biotechnology journal, 2016, 33:59-69.
[19]	MASUDA Y. Auxin-induced cell elongation and cell wall changes[J]. Journal of plant research, 1990, 103(3):345-370.
[20]	WATANABE H, TAKAHASHI K, SAIGUSA M. Morphological and anatomical effects of abscisic acid (ABA) and fluridone (FLU) on the growth of rice mesocotyls[J]. Plant growth regulation, 2011, 34:273-275. doi: 10.1023/A:1013333718573 URL
[21]	XIONG Q, MA B, LU X, et al. Ethylene-inhibited jasmonic acid biosynthesis promotes mesocotyl/coleoptile elongation of etiolated rice seedlings[J]. Plant cell, 2017, 29(5):1053-1072. doi: 10.1105/tpc.16.00981 URL
[22]	YULDASHEV R, AVALBAEV A, BEZRUKOVA M, et al. Cytokinin oxidase is involved in the regulation of cytokinin content by 24-epibrassinolide in wheat seedlings[J]. Plant physiology and biochemistry, 2012, 55:1-6. doi: 10.1016/j.plaphy.2012.03.004 pmid: 22480990
[23]	SUN S, WANG T, WANG L, et al. Natural selection of a GSK3 determines rice mesocotyl domestication by coordinating strigolactone and brassinosteroid signaling[J]. Nature communication, 2018, 9(1):2523. doi: 10.1038/s41467-018-04952-9
[24]	ZHANG X J, LAI Y C, MENG Y, et al. Analyses and identifications of quantitative trait loci and candidate genes controlling mesocotyl elongation in rice[J]. Journal of integrative agriculture, 2023, 22(2):325-340. doi: 10.1016/j.jia.2022.08.080
[25]	OUYANG Y N, ZHANG Q Y, ZHANG K Q, et al. QTL mapping and interaction analysis of genotype/environment (Fe²⁺-concentrations) for mesocotyl length in rice (Oryza sativa L.)[J]. Acta genetica sinica, 2005, 32:712-718.
[26]	WU J, FENG F, LIAN X, et al. Genome-wide association study (GWAS) of mesocotyl elongation based on re-sequencing approach in rice[J]. BMC plant biology, 2015, 15(1):218. doi: 10.1186/s12870-015-0608-0 URL
[27]	ZHAO Y, ZHAO W, JIANG C, et al. Genetic architecture and candidate genes for deep-sowing tolerance in rice revealed by non-syn GWAS[J]. Frontiers in plant science, 2018, 9:332. doi: 10.3389/fpls.2018.00332 pmid: 29616055
[28]	JANG S G, PARK S Y, LAR S M, et al. Genome-wide association study (GWAS) of mesocotyl length for direct seeding in rice[J]. Agronomy, 2021, 11(12):2527. doi: 10.3390/agronomy11122527 URL
[29]	ZHENG J, HONG K, ZENG L, et al. Karrikin signaling acts parallel to and additively with Strigolactone signaling to regulate rice mesocotyl elongation in darkness[J]. Plant cell, 2020, 32(9):2780-2805. doi: 10.1105/tpc.20.00123 URL
[30]	LV Y, SHAO G, JIAO G, et al. Targeted mutagenesis of POLYAMINE OXIDASE 5 that negatively regulates mesocotyl elongation enables the generation of direct-seeding rice with improved grain yield[J]. Molecular plant, 2020, 14:344-351. doi: 10.1016/j.molp.2020.11.007 URL
[31]	LI J, WANG J, ZEIGLER R S. The 3,000 rice genomes project: new opportunities and challenges for future rice research[J]. Giga science, 2014, 3:8. doi: 10.1186/2047-217X-3-8 URL
[32]	WANG W, MAULEON R, HU Z, et al. Genomic variation in 3,010 diverse accessions of Asian cultivated rice[J]. Nature, 2018, 557:43-49. doi: 10.1038/s41586-018-0063-9
[33]	WANG C C, YU H, HUANG J, et al. Towards a deeper haplotype mining of complex traits in rice with RFGB v2.0[J]. Plant biotechnology journal, 2020, 18(1):14-16. doi: 10.1111/pbi.v18.1 URL
[34]	QIAN L, HICKEY L T, STAHL A, et al. Exploring and harnessing haplotype diversity to improve yield stability in crops[J]. Frontiers in plant science, 2017, 8:1534. doi: 10.3389/fpls.2017.01534 pmid: 28928764
[35]	LIU J, ZHAN J, CHEN J, et al. Validation of genes affecting rice grain zinc content through candidate gene-based association analysis[J]. Frontiers in genetics, 2021:1354.
[36]	PRODHOMME C, VOS P G, PAULO M J, et al. Distribution of P1 (D1) wart disease resistance in potato germplasm and GWAS identification of haplotype-specific SNP markers[J]. Theoretical and applied genetics, 2020, 133(6):1859-1871. doi: 10.1007/s00122-020-03559-3
[37]	SINHA P, SINGH V K, SAXENA R K, et al. Superior haplotypes for haplotype-based breeding for drought tolerance in pigeon pea (Cajanus cajan L.)[J]. Plant biotechnology journal, 2020, 18:2482-2490. doi: 10.1111/pbi.v18.12 URL

候选基因	染色体	遗传区间/bp	注释信息
OsGSK2 (LOC_Os05g11730)	5	6657481~6661493	AP2-like ethylene-responsive transcription factor
GY1(LOC_Os01g67430)	1	39177169~39178676	Gibberellin receptor GID1L2
OsPAO5 (LOC_Os04g57560)	4	34244247~34248323	GATA transcription factor 25
OsSMAX1 (LOC_Os08g15230)	8	9224161~9228110	CSLC9 - cellulose synthase-like family C

候选基因	染色体	遗传区间/bp	注释信息
OsGSK2 (LOC_Os05g11730)	5	6657481~6661493	AP2-like ethylene-responsive transcription factor
GY1(LOC_Os01g67430)	1	39177169~39178676	Gibberellin receptor GID1L2
OsPAO5 (LOC_Os04g57560)	4	34244247~34248323	GATA transcription factor 25
OsSMAX1 (LOC_Os08g15230)	8	9224161~9228110	CSLC9 - cellulose synthase-like family C

基因	染色体	位置/bp	参考基因组等位基因	变异等位基因	Hap-1	Hap-2	Hap-3	Hap-4	Hap-5	Hap-6
OsGSK2	5	6661763	G	A	G	G	G	-	-	-
OsGSK2	5	6661820	T	C	T	T	T	-	-	-
OsGSK2	5	6661893	C	T	C	C	C	-	-	-
OsGSK2	5	6662052	C	T	T	C	C	-	-	-
OsGSK2	5	6662421	A	C	A	A	A	-	-	-
OsGSK2	5	6657511	C	T	T	C	C	-	-	-
OsGSK2	5	6657785	G	A	G	G	G	-	-	-
OsGSK2	5	6657996	C	T	C	C	C	-	-	-
OsGSK2	5	6658059	T	C	C	T	T	-	-	-
OsGSK2	5	6661427	G	T	G	G	T	-	-	-
OsPAO5	1	39176236	C	T	C	C	C	-	-	-
OsPAO5	1	39176398	T	G	T	G	T	-	-	-
OsPAO5	1	39176823	A	G	A	A	A	-	-	-
OsPAO5	1	39176859	T	G	T	T	T	-	-	-
OsPAO5	1	39177248	C	T	C	C	C	-	-	-
OsPAO5	1	39177627	C	G	C	C	G	-	-	-
OsPAO5	1	39177801	C	G	C	C	G	-	-	-
OsPAO5	1	39178134	A	C	A	A	C	-	-	-
OsPAO5	1	39178605	T	C	T	T	C	-	-	-
OsPAO5	1	39178663	T	A	T	A	T	-	-	-
GY1	4	34248453	G	A	G	A	R	-	-	-
OsSMAX1	8	9228119	C	T	C	C	C	C	C	C
OsSMAX1	8	9228360	G	A	G	G	A	G	A	G
OsSMAX1	8	9228825	G	A	G	G	G	G	G	G
OsSMAX1	8	9224518	G	A	G	G	A	G	A	G
OsSMAX1	8	9224956	C	G	G	C	C	C	C	G
OsSMAX1	8	9225458	T	C,G	T	T	T	T	T	T
OsSMAX1	8	9225616	G	A	G	-	G	G	G	G
OsSMAX1	8	9226323	T	C	T	T	C	-	C	C
OsSMAX1	8	9226880	G	A	G	G	G	G	R	G
OsSMAX1	8	9227121	A	G	A	A	G	A	G	G

基因	染色体	位置/bp	参考基因组等位基因	变异等位基因	Hap-1	Hap-2	Hap-3	Hap-4	Hap-5	Hap-6
OsGSK2	5	6661763	G	A	G	G	G	-	-	-
OsGSK2	5	6661820	T	C	T	T	T	-	-	-
OsGSK2	5	6661893	C	T	C	C	C	-	-	-
OsGSK2	5	6662052	C	T	T	C	C	-	-	-
OsGSK2	5	6662421	A	C	A	A	A	-	-	-
OsGSK2	5	6657511	C	T	T	C	C	-	-	-
OsGSK2	5	6657785	G	A	G	G	G	-	-	-
OsGSK2	5	6657996	C	T	C	C	C	-	-	-
OsGSK2	5	6658059	T	C	C	T	T	-	-	-
OsGSK2	5	6661427	G	T	G	G	T	-	-	-
OsPAO5	1	39176236	C	T	C	C	C	-	-	-
OsPAO5	1	39176398	T	G	T	G	T	-	-	-
OsPAO5	1	39176823	A	G	A	A	A	-	-	-
OsPAO5	1	39176859	T	G	T	T	T	-	-	-
OsPAO5	1	39177248	C	T	C	C	C	-	-	-
OsPAO5	1	39177627	C	G	C	C	G	-	-	-
OsPAO5	1	39177801	C	G	C	C	G	-	-	-
OsPAO5	1	39178134	A	C	A	A	C	-	-	-
OsPAO5	1	39178605	T	C	T	T	C	-	-	-
OsPAO5	1	39178663	T	A	T	A	T	-	-	-
GY1	4	34248453	G	A	G	A	R	-	-	-
OsSMAX1	8	9228119	C	T	C	C	C	C	C	C
OsSMAX1	8	9228360	G	A	G	G	A	G	A	G
OsSMAX1	8	9228825	G	A	G	G	G	G	G	G
OsSMAX1	8	9224518	G	A	G	G	A	G	A	G
OsSMAX1	8	9224956	C	G	G	C	C	C	C	G
OsSMAX1	8	9225458	T	C,G	T	T	T	T	T	T
OsSMAX1	8	9225616	G	A	G	-	G	G	G	G
OsSMAX1	8	9226323	T	C	T	T	C	-	C	C
OsSMAX1	8	9226880	G	A	G	G	G	G	R	G
OsSMAX1	8	9227121	A	G	A	A	G	A	G	G

基因	TROP群体				TEMP群体
基因	单倍型	数目	比例/%	均值/cm	单倍型	数目	比例/%	均值/cm
OsGSK2	Hap1	248	74.9	1.808	Hap2	146	69.5	0.797
	Hap2	67	20.2	1.64	Hap1	35	16.7	1.221
					Hap3	15	7.1	0.972
GY1	Hap1	221	66.8	1.898	Hap1	181	86.2	0.826
	Hap2	31	9.4	2.205	-	-	-	-
	Hap3	26	7.9	1.105	-	-	-	-
OsPAO5	Hap1	196	59.2	1.679	Hap1	169	80.5	0.801
	Hap2	121	36.6	1.948	Hap2	33	15.7	1.212
	Hap3	11	3.3	1.927	Hap3	5	2.4	0.97
OsSMAX1	Hap1	162	48.9	1.743	Hap1	147	70.0	0.897
	Hap2	43	13.0	2.021	Hap2	28	13.3	0.922
	Hap3	31	9.3	2.271	Hap4	12	5.7	0.848
	Hap4	15	4.5	1.678	-	-	-	-
	Hap5	13	3.9	1.733	-	-	-	-
	Hap6	10	3.0	1.427	-	-	-	-

水稻已克隆中胚轴伸长基因效应解析及优异单倍型鉴定

The Cloned Genes Related to Rice Mesocotyl Elongation: Effects Analysis and Superior Haplotype Identification

RichHTML

PDF (PC)

可视化

摘要/Abstract

引用本文

使用本文

图/表 6

参考文献 37

相关文章 15

编辑推荐

Metrics

本文评价

关于本刊

作者中心

审者中心

在线期刊

联系我们

基因	TROP群体			TEMP群体
基因	优异单倍型	比例/%	均值/cm	优异单倍型	比例/%	均值/cm
OsGSK2	Hap1	74.9	1.81	Hap1	16.7	1.22
GY1	Hap2	9.4	2.21	-	-	-
OsPAO5	Hap3	36.6	1.95	Hap2	15.7	1.21
OsSMAX1	Hap2	13.0	2.02	Hap2	13.3	0.92
OsSMAX1	Hap3	9.3	2.27	-	-	-

[1]	何国和, 陈海斌, 杜建军, 张伟丽, 郭丽华, 胡益波, 颜肇华, 张婧. 化肥减量配施有机肥对粤西地区水稻产量和养分利用的影响[J]. 中国农学通报, 2024, 40(9): 1-8.
[2]	杨小林, 薛敏峰, 张舒, 李进波, 吕亮, 常向前, 张佑宏, 龚艳. 湖北襄阳地区水稻落粒、杆枯等不正常生长现象的解析[J]. 中国农学通报, 2024, 40(8): 112-118.
[3]	李诚, 王少希, 钱艳杰, 易展平, 严小兵. 叶面调理剂在不同镉污染程度稻田应用效果研究[J]. 中国农学通报, 2024, 40(6): 101-106.
[4]	乔月, 胡诚, 万建华, 徐化林, 刘茂军, 郭卫红, 戴黎, 张春华, 邓超然. 不同施肥模式对水稻产量及养分利用效率的影响[J]. 中国农学通报, 2024, 40(6): 9-15.
[5]	徐进, 谭建彬, 邓晓瑜, 梁锦炀, 师沛琼, 周鸿凯. 不同浓度镉处理对耐盐水稻生长及斜纹夜蛾酶活的影响[J]. 中国农学通报, 2024, 40(3): 120-127.
[6]	张喜娟, 王文龙, 孟英, 唐傲, 董文军, 刘猷红, 徐英哲, 王立志, 姜树坤, 杨贤莉, 刘凯, 姜辉, 任洋, 来永才. 种植方式对寒地水稻抗倒伏性状的影响[J]. 中国农学通报, 2024, 40(3): 16-25.
[7]	左雪倩, 谭静, 邓伟, 徐雨然, 吕莹, 张锦文, 余琴, 董维, 管俊娇, 李小林. 云南省杂交籼稻品种试验分析[J]. 中国农学通报, 2024, 40(3): 8-15.
[8]	阚建鸾, 石吕, 韩笑, 周志宏, 苏建平, 刘建, 薛亚光. 减氮和侧深基施缓混肥对‘南粳5055’产量、品质及氮素吸收利用的影响[J]. 中国农学通报, 2024, 40(2): 91-96.
[9]	程新杰, 施伟, 张梦龙, 岳红亮, 代金英, 胡蕾, 朱国永. 水稻垩白形成机制的研究进展[J]. 中国农学通报, 2024, 40(2): 1-7.
[10]	邹积祥, 杨陶陶, 伍龙梅, 包晓哲, 张彬. 华南地区早晚兼用型水稻产量和氮素吸收在早、晚季的差异特征[J]. 中国农学通报, 2024, 40(12): 1-8.
[11]	黄金玲, 覃丽萍, 刘志明, 刘峥嵘, 李红芳, 陆秀红. 广西水稻产区稻-菜轮作田水稻根结线虫病发生情况调查及病原鉴定[J]. 中国农学通报, 2024, 40(12): 126-133.
[12]	赵晴, 欧英卓, 胡诗钦, 周宇阳, 郭龙彪, 郝芷圻, 孟丽君, 刘长华. 水稻耐盐生理及分子机制研究进展[J]. 中国农学通报, 2024, 40(12): 94-103.
[13]	陈书健, 陈京都, 杨呈芹, 许美刚, 高剑波. 不同施氮量对机械水条播水稻产量及品质的影响[J]. 中国农学通报, 2023, 39(9): 1-6.
[14]	赵首萍, 肖文丹, 陈德, 叶雪珠, 张棋, 伍少福, 胡静, 高娜, 黄淼杰. 基于土壤质量和稻米安全的稻田重金属钝化效果评估[J]. 中国农学通报, 2023, 39(8): 51-62.
[15]	刘伟喜, 尹文锋, 李小娟, 肖友伦. 旱改水田水稻旱青立病的发生原因及防治措施研究[J]. 中国农学通报, 2023, 39(8): 85-89.