Scientia Agricultura Sinica ›› 2020, Vol. 53 ›› Issue (6): 1081-1094.doi: 10.3864/j.issn.0578-1752.2020.06.001

• CROP GENETICS & BREEDING·GERMPLASM RESOURCES·MOLECULAR GENETICS • Previous Articles     Next Articles

Transcriptome Research of Erect and Short Panicle Mutant esp in Rice

KunNeng ZHOU,JiaFa XIA,Peng YUN,YuanLei WANG,TingChen MA,CaiJuan ZHANG,ZeFu LI()   

  1. Rice Research Institute, Anhui Academy of Agricultural Sciences/Key Laboratory for Rice Genetics and Breeding of Anhui Province, Hefei 230001
  • Received:2019-08-05 Accepted:2019-10-21 Online:2020-03-16 Published:2020-04-09
  • Contact: ZeFu LI E-mail:lizefu@aliyun.com

Abstract:

【Objective】In this study, we aimed to identify the ESP gene, whose mutation caused a phenotype, namely erect and short panicle, and to determine its regulatory role in the gene network that controls the related agronomic traits (e.g., plant types and panicle length).【Method】In this study, agronomic traits, such as plant height, panicle length and grain length at mature stages, were used as phenotypic marks to trace the esp mutant. Individuals carrying mutant phenotypes were selected from the F2 population to cross with indica and japonica for further gene mapping and genome sequencing that were used to map the potential mutation region/sites. The bioinformatics software was used to analyze phylogenetic tree and gene expression. The total RNAs isolated from wild type and mutants were used for transcriptome RNA-seq analysis. The differential expressed genes and expression levels of genes related to plant hormone signal transduction and protein processing in endoplasmic reticulum were analyzed by GO software and KEGG database. The transcriptome data were verified by qRT-PCR.【Result】Phenotypic analysis showed that the esp mutant exhibited a erect panicle architecture. The plant height, panicle length, grain length and the number of spikelets per panicle were decreased in the esp mutants, when compared to wild type control, whereas grain width and the 1 000-grain weight were increased, although no obvious difference in the number of effective panicles between mutants and control. The ESP gene was mapped to a 7.58 Mb interval between markers C7-11 and C7-14 on the long arm of rice 7th chromosome by using the F2 population of esp mutant and PA64. Genome sequencing demonstrated that a single nucleotide change (G to A) at the junction of 6th intron and 7th exon of LOC_Os07g42410, which led to a splicing defect, causing premature protein translation. The ESP was allelic to OsDEP2/OsEP2. Phylogenetic analysis revealed that the ESPs are widely present in monocot and dicot plants. Expression analysis predicted that ESP gene was highly expressed in stem, inflorescence, pistil, glumelle, lemma and ovary, and the expression level was gradually decreased with the ovary inflation. Transcriptome RNA-seq analysis of young panicle identified 630 differential expressed genes in esp mutants versus wild type, including 235 up-regulated and 395 down-regulated. GO and qRT-PCR analysis revealed that genes involved in plant hormone signal transduction and protein processing in endoplasmic reticulum were misregulated in esp mutants.【Conclusion】The ESP gene was allelic to OsDEP2/OsEP2, the mutation of which leads to multiple phenotypes, such as decreased plant height and shorter panicle length. Transcriptome analysis suggested that the ESP gene might affect plant development by regulating genes expression associated with plant hormone signal transduction and protein processing in endoplasmic reticulum.

Key words: rice (Oryza sativa L.), erect and short panicle mutant, gene cloning, phylogenetic analysis, transcriptome analysis

Table 1

Agronomic traits of the esp mutant and WT"

农艺性状Agronomic traits 野生型WT 突变体esp
株高Plant height (cm) 79.1±1.7 67.2±1.5**
有效穗数Number of effective panicles 14.8±1.7 14.9±1.2
穗长Panicle length (cm) 21.06±0.85 17.03±0.70**
每穗粒数Grain number per panicle 190.5±15.2 136.7±8.8**
剑叶长Flag leaf length (cm) 26.60±1.53 36.07±2.64**
剑叶宽Flag leaf width (cm) 1.86±0.05 1.83±0.08
千粒重1000-grain weight (g) 24.33±0.34 25.34±0.42*

Fig. 1

Phenotypic characteristics of the esp mutant and wild type (WT) A: Plant phenotypes of mature stage; B: Panicle phenotypes of mature stage; C, D and E: Determination of seed width and length"

Fig. 2

Map-based cloning of the ESP gene A: Initial mapping of the ESP gene; B: Structure of the ESP gene and mutant site of esp; ATG and TGA indicate start and stop codons, respectively"

Fig. 3

Phylogenetic analysis of ESP and its related proteins"

Fig. 4

Expression analysis of ESP gene A: Expression profile of ESP gene in different tissues at various stages; B: Expression analysis of ESP gene during the progress of ovary development; Data were collected from the rice expression profile database, RiceXPro"

Fig. 5

Transcriptome analysis of young panicles in esp mutant and WT A: Volcano Plot of transcriptome analysis of young panicles in esp mutant and wild type; Red and green dots separately represent up- and down-regulated genes, blue dots indicate genes with no significant difference; B: Numbers of up-regulated and down-regulated genes expressed differentially more than 1.5 time; C: Functional classification of differentially expressed genes"

Table 2

Metabolic pathways and the number of differentially expressed genes"

序号 No. 通路名称 Pathway name 差异基因数 DEGs PP value
1 次生代谢产物生物合成 Biosynthesis of secondary metabolites 86 5.47×10-3
2 乙醛酸和二羧酸代谢 Glyoxylate and dicarboxylate metabolism 12 6.19×10-3
3 淀粉和蔗糖代谢 Starch and sucrose metabolism 22 8.09×10-3
4 内质网蛋白加工 Protein processing in endoplasmic reticulum 28 9.59×10-3
5 苯丙素生物合成 Phenylpropanoid biosynthesis 19 1.30×10-2
6 脂肪酸伸长 Fatty acid elongation 6 2.36×10-2
7 植物激素信号转导 Plant hormone signal transduction 24 2.69×10-2
8 氮代谢 Nitrogen metabolism 6 3.63×10-2
9 氰基氨基酸代谢 Cyanoamino acid metabolism 7 4.23×10-2
10 酪氨酸代谢 Tyrosine metabolism 7 4.71×10-2
11 丙氨酸、天冬氨酸和谷氨酸代谢 Alanine, aspartate and glutamate metabolism 7 6.99×10-2

Fig. 6

Expression analysis of genes related to plant hormone signal transduction A: Pathway of plant hormone signal transduction; B: Expression of genes related to plant hormone signal transduction in transcriptome analysis"

Fig. 7

Expression analysis of genes related to protein processing in endoplasmic reticulum A: Pathway of protein processing in endoplasmic reticulum; B: Expression of genes related to protein processing of endoplasmic reticulum in transcriptome analysis"

Fig. 8

Quantitative PCR analysis of genes involved in plant hormone signal transduction and protein processing of endoplasmic reticulum between mutant and WT A: Expression analysis of genes related to plant hormone signal transduction; B: Expression analysis of genes related to protein processing of endoplasmic reticulum; * and ** separately indicate significance at P=0.05 and P=0.01 by Student's t test"

Table 3

Phenotypic characteristics of ESP allelic mutant"

突变体
Mutant
野生型
Wild type
株高
Plant height
穗长
Panicle length
每穗粒数
Grain number per panicle
粒长
Grain length
粒宽
Grain width
千粒重
1000-grain weight
esp 宁粳36(粳)
Ningjing 36 (Japonica)
降低
Decrease
变短
Shorten
减少
Reduce
降低
Decrease
增加
Increase
轻微增加
Slightly increase
ep2-1 中籼3037(籼)
Zhongxian 3037 (Indica)
降低
Decrease
变短
Shorten
减少
Reduce
降低
Decrease
增加
Increase
降低
Decrease
ep2-2 9311(籼)
9311 (Indica)
降低
Decrease
变短
Shorten
增加
Increase
降低
Decrease
增加
Increase
轻微降低
Slightly decrease
dep2-1/dep2-2 中花11/日本晴(粳)
Zhonghua 11/Nipponbare (Japonica)
降低
Decrease
变短
Shorten
无差别
No difference
降低
Decrease
增加
Increase
降低
Decrease
[1] ASHIKARI M, SAKAKIBARA H, LIN S, YAMAMOTO T, TAKASHI T, NISHIMURA A, ANGELES E R, QIAN Q, KITANO H, MATSUOKA M . Cytokinin oxidase regulates rice grain production. Science, 2005,309:741-745.
[2] JIN J, HUANG W, GAO J P, YAN J, SHI M, ZHU M Z, LUO D, LIN H X . Genetic control of rice plant architecture under domestication. Nature Genetics, 2008,40:1365-1369.
[3] LI P, WANG Y, QIAN Q, FU Z, WANG M, ZENG D, LI B, WANG X, LI J . LAZY1 controls rice shoot gravitropism through regulating polar auxin transport. Cell Research, 2007,17:402-410.
[4] LI S, QIAN Q, FU Z, ZENG D, MENG X, KYOZUKA J, MAEKAWA M, ZHU X, ZAHNG J, LI J, WANG Y . Short panicle1 encodes a putative PTR family transporter and determines rice panicle size. The Plant Journal, 2009,58:592-605.
[5] YU B, LIN Z, LI H, LI X, LI J, WANG Y, ZHANG X, ZHU Z, ZHAI W, WANG X, XIE D, SUN C . TAC1, a major quantitative trait locus controlling tiller angle in rice. The Plant Journal, 2007,52:891-898.
[6] HUANG X, QIAN Q, LIU Z, SUN H, HE S, LUO D, XIA G, CHU C, LI J, FU X . Natural variation at the DEP1 locus enhances grain yield in rice. Nature Genetics, 2009,41:494-497.
[7] YAN C J, ZHOU J H, YAN S, CHEN F, YEBOAH M, TANG S Z, LIANG G H, GU M H . Identification and characterization of a major QTL responsible for erect panicle trait in japonica rice,(Oryza sativa L.). Theoretical and Applied Genetics, 2007,115:1093-1100.
[8] ZHOU Y, ZHU J, LI Z, YI C, LIU J, ZHANG H, TANG S, GU M, LIANG G . Deletion in a quantitative trait gene qPE9-1 associated with panicle erectness improves plant architecture during rice domestication. Genetics, 2009,183:315-324.
[9] SUN H, QIAN Q, WU K, LUO J, WANG S, ZHANG C, MA Y, LIU Q, HUANG X, YUAN Q, HAN R, ZHAO M, DONG G, GUO L, ZHU X, GOU Z, WANG W, WU Y, LIN H, FU Q . Heterotrimeric G proteins regulate nitrogen-use efficiency in rice. Nature Genetics, 2014,46:652-656.
[10] YI X, ZHANG Z, ZENG S, TIAN C, PENG J, LI M, LU Y, MENG Q, GU M, YAN C . Introgression of qPE9-1 allele, conferring the panicle erectness, leads to the decrease of grain yield per plant in japonica rice (Oryza sativa L.). Journal of Genetics and Genomics, 2011,38:217-223.
[11] LIU Q, HAN R, WU K, ZHANG J, YE Y, WANG S, CHEN J, PAN Y, LI Q, XU X, ZHOU J, TAO D, WU Y, FU X . G-protein βγ subunits determine grain size through interaction with MADS-domain transcription factors in rice. Nature Communication, 2018,9:852.
[12] 陈温福, 徐正进, 张龙步, 张文忠, 马殿荣 . 北方粳型稻超高产育种理论与实践. 中国农业科学, 2007,40(5):869-874.
CHEN W F, XU Z J, ZHANG L B, ZHANG W Z, MA D R . Theories and practices of breeding japonica rice for super high yield. Scientia Agricultura Sinica, 2007,40(5):869-874. (in Chinese)
[13] WANG J, NAKAZAKI T, CHEN S, CHEN W, SAITO H, TSUKIYAMA T, OKUMOTO Y, XU Z, TANISAKA T . Identification and characterization of the erect-pose panicle gene EP conferring high grain yield in rice,(Oryza sativa L.). Theoretical and Applied Genetics, 2009,119:85-91.
[14] LI F, LIU W, TANG J, CHEN J, TONG H, HU B, LI C, FANG J, CHEN M, CHU C . Rice DENSE AND ERECT PANICLE 2 is essential for determining panicle outgrowth and elongation. Cell Research, 2010,20:838-849.
[15] ZHU K, TANG D, YAN C, CHI Z, YU H, CHEN J, LIANG J, GU M, CHENG Z . ERECT PANICLE2 encodes a novel protein that regulates panicle erectness in indica rice. Genetics, 2010,184:343-350.
[16] ABE Y, MIEDA K, ANDO T, KONO I, YANO M, KITANO H, IWASAKI Y . The SMALL AND ROUND SEED1 (SRS1/DEP2) gene is involved in the regulation of seed size in rice. Genes and Genetic Systems, 2010,85:327-339.
[17] 朱海涛, 柯善文, 冯小龙, 邹龙海, 曾秀瑜, 张向前 . 水稻直立穗突变体ep7的鉴定及其候选基因分析. 华北农学报, 2014,29(4):44-48.
ZHU H T, KE S W, FENG X L, ZOU L H, ZENG X Y, ZHANG X Q . Identification of an erect panicle mutant ep7 in rice and analysis of the candidate gene. Acta Agricultura Boreali-Sinica, 2014,29(4):44-48. (in Chinese)
[18] QIAO Y, PIAO R, SHI J, LEE S I, JIANG W, KIM B K, LEE J, HAN L, MA W, KOH H J . 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, 2011,122:1439-1449.
[19] PIAO R, JIANG W, HAM T H, CHOI M S, QIAO Y, CHU S H, PARK J H, WOO M O, JIN Z, AN G, LEE J, KOH H J . Map-based cloning of the ERECT PANICLE 3 gene in rice. Theoretical and Applied Genetics, 2009,119:1497-1506.
[20] YU H, MURCHIE E H GONZALEZ-CARRANZA Z H, PYKE K A, ROBERTS J A . Decreased photosynthesis in the erect panicle 3 (ep3) mutant of rice is associated with reduced stomatal conductance and attenuated guard cell development. Journal of Experimental Botany, 2015,66(5):1543-1552.
[21] 朱金燕, 王军, 杨杰, 范方军, 杨金欢, 仲维功 . 一个与水稻直立穗基因qPE9-1关联的InDel标记的设计与验证. 分子植物育种, 2012,10(5):583-588.
ZHU J Y, WANG J, YANG J, FAN F J, YANG J H, ZHONG W G . Development and application for a functional marker for erect panicle gene qPE9-1 of rice. Molecular Plant Breeding, 2012,10(5):583-588. (in Chinese)
[22] 胡运高, 郭连安, 杨国涛, 钦鹏, 范存留, 彭友林, 严维, 何航, 李仕贵 . 直立密穗基因DEP2-1388的遗传分析及在杂交稻中的育种利用. 遗传, 2016,38(1):72-81.
HU Y G, GUO L A, YANG G T, QIN P, FAN C L, PENG Y L, YAN W, HE H, LI S G . Genetic analysis of dense and erect panicle 2 alleleDEP2-1388 and its application in hybrid rice breeding. Hereditas, 2016,38(1):72-81. (in Chinese)
[23] ISHIMARU K, HIROTSU N, MADOKA Y, MURAKAMI N, HARA N, ONODERA H, KASHIWAGI T, UJIIE K, SHIMIZU B, ONISHI A, MIYAGAWA H, KATOH E . Loss of function of the IAA-glucose hydrolase gene TGW6 enhances rice grain weight and increases yield. Nature Genetics, 2013,45(6):707-711.
[24] ZHANG S, WANG S, XU Y, YU C, SHEN C, QIAN Q, GEISLER M, JIANG DE A, QI Y . The auxin response factor, OsARF19, controls rice leaf angles through positively regulating OsGH3-5 and OsBRI1. Plant Cell and Environment, 2015, 38(4):638-654.
[25] ZHANG S, WU T, LIU S, LIU X, JIANG L, WAN J . Disruption of OsARF19 is critical for floral organ development and plant architecture in rice ( Oryza sativa L.). Plant Molecular Biology Reporter, 2016,34(4):748-760.
[26] JIN J, HUA L, ZHU Z, TAN L, ZHAO X, ZHANG W, LIU F, FU Y, CAI H, SUN X, GU P, XIE D, SUN C . GAD1 encodes a secreted peptide that regulates grain number, grain length and awn development in rice domestication. The Plant Cell, 2016,28(10):2453-2463.
[27] TAGUCHI-SHIOBARA F, KAWAGOE Y, KATO H, ONODERA H, TAGIRI A, HARA N, MIYAO A, HIROCHIKA H, KITANO H, YANO M, TOKI S . A loss-of-function mutation of rice DENSE PANICLE 1 causes semi-dwarfness and slightly increased number of spikelets. Breeding Science, 2011,61(1):17-25.
[28] 赵明珠, 王青营, 孙健, 徐正进, 陈温福 . 水稻直立穗型基因DEP1研究进展. 中国科学: 生命科学, 2017,47(10):1036-1042.
ZHAO M Z, WANG Q Y, SUN J, XU Z J, CHEN W F . Research progress of rice erect panicle gene DEP1. Scientia Sinica Vitae, 2017,47(10):1036-1042. (in Chinese)
[29] 高士杰, 陈温福, 张龙步 . 直立穗型水稻的研究. 吉林农业科学, 1999,24(6):12-15.
GAO S J, CHEN W F, ZHANG B L . Studies of erect panicle in rice. Journal of Jilin Agricultural Science, 1999,24(6):12-15. (in Chinese)
[30] WANG Y, LI J . Molecular basis of plant architecture. Annual Review of Plant Biology, 2008,59:253-279.
[31] XU Z J, CHEN W F, ZHANG L B, YANG S R . Design principles and parameters of rice ideal panicle type. Chinese Science Bulletin, 2005,50:2253-2256.
[1] GU LiDan,LIU Yang,LI FangXiang,CHENG WeiNing. Cloning of Small Heat Shock Protein Gene Hsp21.9 in Sitodiplosis mosellana and Its Expression Characteristics During Diapause and Under Temperature Stresses [J]. Scientia Agricultura Sinica, 2023, 56(1): 79-89.
[2] LI YuZe,ZHU JiaWei,LIN Wei,LAN MoYing,XIA LiMing,ZHANG YiLi,LUO Cong,HUANG Gui Xiang,HE XinHua. Cloning and Interaction Protein Screening of RHF2A Gene from Xiangshui Lemon [J]. Scientia Agricultura Sinica, 2022, 55(24): 4912-4926.
[3] ZHAO ChunFang,ZHAO QingYong,LÜ YuanDa,CHEN Tao,YAO Shu,ZHAO Ling,ZHOU LiHui,LIANG WenHua,ZHU Zhen,WANG CaiLin,ZHANG YaDong. Screening of Core Markers and Construction of DNA Fingerprints of Semi-Waxy Japonica Rice Varieties [J]. Scientia Agricultura Sinica, 2022, 55(23): 4567-4582.
[4] QU Cheng,WANG Ran,LI FengQi,LUO Chen. Cloning and Expression Profiling of Gustatory Receptor Genes BtabGR1 and BtabGR2 in Bemisia tabaci [J]. Scientia Agricultura Sinica, 2022, 55(13): 2552-2561.
[5] ZHANG Li,ZHANG Nan,JIANG HuQiang,WU Fan,LI HongLiang. Molecular Cloning and Expression Pattern Analysis of NPC2 Gene Family of Apis cerana cerana [J]. Scientia Agricultura Sinica, 2022, 55(12): 2461-2471.
[6] ZHANG YaDong,LIANG WenHua,HE Lei,ZHAO ChunFang,ZHU Zhen,CHEN Tao,ZHAO QingYong,ZHAO Ling,YAO Shu,ZHOU LiHui,LU Kai,WANG CaiLin. Construction of High-Density Genetic Map and QTL Analysis of Grain Shape in Rice RIL Population [J]. Scientia Agricultura Sinica, 2021, 54(24): 5163-5176.
[7] ZHANG Lu,ZONG YaQi,XU WeiHua,HAN Lei,SUN ZhenYu,CHEN ZhaoHui,CHEN SongLi,ZHANG Kai,CHENG JieShan,TANG MeiLing,ZHANG HongXia,SONG ZhiZhong. Identification, Cloning, and Expression Characteristics Analysis of Fe-S Cluster Assembly Genes in Grape [J]. Scientia Agricultura Sinica, 2021, 54(23): 5068-5082.
[8] TAN YongAn,JIANG YiPing,ZHAO Jing,XIAO LiuBin. Expression Profile of G Protein-Coupled Receptor Kinase 2 Gene (AlGRK2) and Its Function in the Development of Apolygus lucorum [J]. Scientia Agricultura Sinica, 2021, 54(22): 4813-4825.
[9] WANG Na,ZHAO ZiBo,GAO Qiong,HE ShouPu,MA ChenHui,PENG Zhen,DU XiongMing. Cloning and Functional Analysis of Salt Stress Response Gene GhPEAMT1 in Upland Cotton [J]. Scientia Agricultura Sinica, 2021, 54(2): 248-260.
[10] XU ZiYi,CHENG Xing,SHEN Qi,ZHAO YaNan,TANG JiaYu,LIU Xi. Identification and Gene Functional Analysis of Yellow Green Leaf Mutant ygl3 in Rice [J]. Scientia Agricultura Sinica, 2021, 54(15): 3149-3157.
[11] REN ZhiJie,LI Qian,SUN YuJia,KONG DongDong,LIU LiangYu,HOU CongCong,LI LeGong. OsCSC11 Mediates Dry-Hot Wind/Drought-Induced Ca2+ Signal to Regulate Stamen Development in Rice [J]. Scientia Agricultura Sinica, 2021, 54(10): 2039-2052.
[12] TAN YongAn,ZHAO XuDong,JIANG YiPing,ZHAO Jing,XIAO LiuBin,HAO DeJun. Cloning, Preparation of Antibody and Response Induced by 20-Hydroxyecdysone of Target of Rapamycin in Apolygus lucorum [J]. Scientia Agricultura Sinica, 2021, 54(10): 2118-2131.
[13] YU AiLi,ZHAO JinFeng,CHENG Kai,WANG ZhenHua,ZHANG Peng,LIU Xin,TIAN Gang,ZHAO TaiCun,WANG YuWen. Screening and Analysis of Key Metabolic Pathways in Foxtail Millet During Different Water Uptake Phases of Germination [J]. Scientia Agricultura Sinica, 2020, 53(15): 3005-3019.
[14] SHEN JingYuan,TANG MeiLing,YANG QingShan,GAO YaChao,LIU WanHao,CHENG JieShan,ZHANG HongXia,SONG ZhiZhong. Cloning, Expression and Electrophysiological Function Analysis of Potassium Channel Gene VviSKOR in Grape [J]. Scientia Agricultura Sinica, 2020, 53(15): 3158-3168.
[15] WANG FangQuan,CHEN ZhiHui,XU Yang,WANG Jun,LI WenQi,FAN FangJun,CHEN LiQin,TAO YaJun,ZHONG WeiGong,YANG Jie. Development and Application of the Functional Marker for the Broad-Spectrum Blast Resistance Gene PigmR in Rice [J]. Scientia Agricultura Sinica, 2019, 52(6): 955-967.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!