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作物学报 ›› 2023, Vol. 49 ›› Issue (12): 3399-3410.doi: 10.3724/SP.J.1006.2023.31004

• 研究简报 • 上一篇    

小麦卷叶突变体RL1的生理特性及遗传研究

刘叶1,2(), 李越1, 苑名杨1, 卫乃翠1, 关攀锋3, 赵佳佳1, 武棒棒1, 郑兴卫1, 郝宇琼1, 乔玲1,*(), 郑军1,*()   

  1. 1山西农业大学小麦研究所 / 农业农村部有机旱作农业重点实验室(部省共建), 山西临汾 041000
    2山西大学生命科学学院, 山西太原 030006
    3郑州大学农学院, 河南郑州 450001
  • 收稿日期:2023-01-09 接受日期:2023-06-29 出版日期:2023-12-12 网络出版日期:2023-08-04
  • 通讯作者: * 乔玲, E-mail: qiaolingsmile@163.com; 郑军, E-mail: sxnkyzj@126.com
  • 作者简介:刘叶, E-mail: liuye12345202@126.com**同等贡献
  • 基金资助:
    山西农业大学省部共建有机旱作农业国家重点实验室自主研发项目(202002-1);山西省科技重大专项计划“揭榜挂帅”项目(202201140601025-2-01)

Physiological characteristics and genetic research of rolled leaf mutant1 (RL1) in wheat (Triticum aestivum L.)

LIU Ye1,2(), LI Yue1, YUAN Ming-Yang1, WEI Nai-Cui1, GUAN Pan-Feng3, ZHAO Jia-Jia1, WU Bang-Bang1, ZHENG Xing-Wei1, HAO Yu-Qiong1, QIAO Ling1,*(), ZHENG Jun1,*()   

  1. 1Institute of Wheat Research, Shanxi Agriculture University / Key Laboratory of Sustainable Dryland Agriculture (Co-construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Linfen 041000, Shanxi, China
    2School of Life Science, Shanxi University, Taiyuan 030006, Shanxi, China
    3School of Agricultural Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China
  • Received:2023-01-09 Accepted:2023-06-29 Published:2023-12-12 Published online:2023-08-04
  • Contact: * E-mail: qiaolingsmile@163.com; E-mail: sxnkyzj@126.com
  • About author:**Contributed equally to this work
  • Supported by:
    Research Program Sponsored by State Key Laboratory of Integrative Sustainable Dryland Agriculture, Shanxi Agricultural University(202002-1);Science and Technology Major Special Plan Project “Reveal the Title” of Shanxi Province(202201140601025-2-01)

摘要:

小麦叶片在逆境下会发生可逆的折叠或卷曲, 通过脱水回避的形态学变化降低非生物胁迫的损害。目前小麦叶片卷曲的生理和遗传调控机制尚不清楚。本文利用EMS诱变晋麦47获得了卷叶突变体RL1 (Rolled Leaf 1), RL1在整个生育期叶片呈现卷曲, 初生叶片沿中轴脉向近轴面微卷, 随着叶片生长加速卷曲, 直至为筒状。与野生型相比, RL1株高降低、穗长变短、旗叶变窄和千粒重降低。氯化三苯基四氮唑(TTC)染色结果表明RL1种子活力低, 且种子发芽率降低了22%。抽穗10 d后, RL1的叶绿素含量与野生型基本一致, 净光合速率、蒸腾速率、气孔导度、细胞间隙CO2浓度差异不显著, 但水分利用率降低。低温、高温和干旱促进RL1的叶片卷曲; 石蜡切片观察表明, RL1的大叶脉和小叶脉偏少, 在中脉区域远轴面厚壁细胞和近轴面薄壁细胞数目减少, 且维管束间泡状细胞的面积和数量均明显低于野生型; RL1叶片不同部位泡状细胞缩小以及维管束减少导致整个叶片向近轴面极度卷曲。遗传分析表明该性状受1对不完全显性的核基因控制, 位于1D染色体短臂上, 精细定位将目标区间锁定在9.42 Mb范围内。

关键词: 小麦, 卷叶突变体, 细胞学分析, 生理特性, 遗传分析

Abstract:

Wheat leaves tend to fold or curl when exposure to stresses, the dehydration avoidance in morphology can reduce the damage of abiotic stress. At present, the physiological and genetic regulation mechanism associated with leaf curling is not clear in wheat. This study reported a novel rolled leaf mutant (RL1) from the ethyl methyl sulphonate (EMS) mutagenesis cultivar Jinmai 47. The leaves of the mutant RL1 were curled during the growth period, and the primary leaves were slightly curled along axial vein to paraxial plane. Leaf curling was accelerated with the growth until the leaf was tubular. Compared to wild type (WT), plant height, ear length, flag leaf narrowing, and 1000-grain weight were decreased in mutant RL1. Triphenyltetrazolium Chloride (TTC) staining showed that seed vigor of RL1 was low, together with the decreased germination rate by 22%. Additionally, there was no significant differences in chlorophyll content, net photosynthetic rate, transpiration rate, stomatal conductance, and intercellular CO2 concentration between RL1 and WT, while water utilization rate was decreased in RL1 after heading for 10 days. Low temperature, high temperature, and drought led to the leaf rolling in RL1. RL1 showed fewer leaf/lobular veins via paraffin section assay, and the number of abaxial sclerenchyma and adaxial parenchyma cells were reduced in midrib region of RL1. Moreover, the area and counts of vesicular cells between the vascular bundles were significantly reduced in RL1, together with the vesicular cells at the midvein region of leaves compared with WT. Vesicular cells and vascular bundles shrunk and decreased, respectively, resulting in the situation that the entire blade was extremely crimped to the adaxial plane. Genetic analysis demonstrated that the mutant trait was localized on the short arm of chromosome 1D, regulated by a pair of nuclear genes with incomplete dominance and fine mapping analysis further locked the target interval at 9.42 Mb.

Key words: wheat, rolled leaf mutant, cytological analysis, physiological characteristics, genetic analysis

表1

KASP标记序列"

标记 Marker SNP F1 F2 R
RLB T/C CCAACCCTAGCTTGTGATCCC TCCAACCCTAGCTTGTGATCCT AGGGGCCCACAAGCCTCCTG
RLC C/G GAATCACGAAAGCACCCTCGC GAATCACGAAAGCACCCTCGG GGCAAACGTGTAGATCGTCTCCC
RLF A/C CGTAACATACAACCATGCCTACCT GTAACATACAACCATGCCTACCG CGTTCAAGGGTTCACATAAGGCTTTTG
RLH A/C GTGGCATGTCAACTCGCGATTTATA GGCATGTCAACTCGCGATTTATC CAACTGAGTGGCATATATATAGTCTGTTATA
RLI A/C CAGAATCACTTCTTGACTACCCCAA GAATCACTTCTTGACTACCCCAC CAGCCTTCTAGAGCCACATTCTAGTA
RLJ T/C GTGCTCCTAGGAAGTAGGAGC ATGTGCTCCTAGGAAGTAGGAGT CCAAAAGCAAGGACGCTTCCAGG
RLK T/C TATTTTGAGACGAAGAGAGAATCGTG ATTTATTTTGAGACGAAGAGAGAATCGTA AGGCGGGTGCTTGCCCTTACAT
RLO C/G TTATACTAAAGCTGCATCAATTAACTTGC TTATACTAAAGCTGCATCAATTAACTTGG GGGCAGTACAACAAACATCAGAAATAAC

附表1

42对SSR引物信息(国标: NY/T 2859-2015)"

引物名称
Primer name
染色体
Chr.
退火温度
Annealing temperature (℃)
引物序列
Primer sequence
(5'-3')
cwm65 1A 65 F: TCATTGGTGTCATCCCTCGTGT; R: GAATAATGCCTTGACCCTGGAC
barc80 1BL 65 F: GCGAATTAGCATCTGCATCTGTTTGAG; R: CGGTCAACCAACTACTGCACAAC
cfd72 1DL 60 F: CTCCTTGGAATCTCACCGAA; R: TCCTTGGGAATATGCCTCCT
gwm294 2AL 55 F: GGATTGGAGTTAAGAGAGAACCG; R: GCAGAGTGATCAATGCCAGA
gwm429 2BS 55 F: TTGTACATTAAGTTCCCATTA; R: TTTAAGGACCTACATGACAC
gwm261 2DS 55 F: CTCCCTGTACGCCTAAGGC; R: CTCGCGCTACTAGCCATTG
gwm155 3AL 55 F: CAATCATTTCCCCCTCCC; R: AATCATTGGAAATCCATATGCC
gwm285 3BS 65 F: ATGACCCTTCTGCCAAACAC; R: ATCGACCGGGATCTAGCC
gdm72 3DS 55 F: TGGTTTTCTCGAGCATTCAA; R: TGCAACGATGAAGACCAGAA
gwm610 4AS 65 F: CTGCCTTCTCCATGGTTTGT; R: AATGGCCAAAGGTTATGAAGG
ksum62 4B 60 F: GGAGAGGATAGGCACAGGAC; R: GAGAGCAGAGGGAGCTATGG
barc91 4DL 55 F: TTCCCATAACGCCGATAGTA; R: GCGTTTAATATTAGCTTCAAGATCAT
gwm304 5AS 55 F: AGGAAACAGAAATATCGCGG; R: AGGACTGTGGGGAATGAATG
gwm67 5BL 60 F: ACCACACAAACAAGGTAAGCG; R: CAACCCTCTTAATTTTGTTGGG
cfd29 5DL 65 F: GGTTGTCAGGCAGGATATTTG; R: TATTGATAGATCAGGGCGCA
gwm459 6AS 55 F: AATTTCAAAAAGGAGAGAGA; R: AACATGTGTTTTTAGCTATC
barc198 6BS 55 F: CGCTGAAAAGAAGTGCCGCATTATGA; R: CGCTGCCTTTTCTGGATTGCTTGTCA
cfd76 6DL 65 F: GCAATTTCACACGCGACTTA; R: CGCTCGACAACATGACACTT
cfa2028 7AS 55 F: TGGGTATGAAAGGCTGAAGG; R: ATCGCGACTATTCAACGCTT
gwm333 7BS 60 F: GCCCGGTCATGTAAAACG; R: TTTCAGTTTGCGTTAAGCTTTG
gwmn437 7DL 55 F: GATCAAGACTTTTGTATCTCTC; R: GATGTCCAACAGTTAGCTTA
wmc312 1AS 55 F: TGTGCCCGCTGGTGCGAAG; R: CCGACGCAGGTGAGCGAAG
barc240 1BL 55 F: AGAGGACGCTGAGAACTTTAGAGAA; R: GCGATCTTTGTAATGCATGGTGAAC
gdm111 1DL 55 F: CACTCACCCCAAACCAAAGT; R: GATGCAATCGGGTCGTTAGT
wmc522 2AS 55 F: AAAAATCTCACGAGTOGGGC; R: CCCGAGCAGGAGCTACAAAT
cfd51 2DS 55 F: GGAGGCTTCTCTATGGGAGG; R: TGCATCTTATCCTGTGCAGC
barc324 3AS 55 F: CCAATTCTGCCCATAGGTGA; R: GAGGAAATAAGATTCAGCCAACTG
barc164 3BS 55 F: TGCAAACTAATCACCAGCGTAA; R: CGCTTTCTAAAACTGTTCGGGATTTCTAA
cfd9 3DL 55 F: TTGCACGCACCTAAACTCTG; R: CAAGTGTGAGCGTCGG
gwm161 3DS 55 F: GATCGAGTGATGGCAGATGG; R: TGTGAATTACTTGGACGTGG
barc170 4AL 55 F: CGCTTGACTTTGAATGGCTGAACA; R: CGCCCACTTTTTACCTAATCCTTTTGAA
gwm495 4BL 55 F: GAGAGCCTCGCGAAATATAGG; R: TGCTTCTGGTGTTCCTTCG
winc720 4DS 55 F: CACCATGGTTGGCAAGAGA; R: CTGGTGATACTGCCGTGACA
gwm186 5AL 55 F: GCAGAGCCTGGTTCAAAAAG; R: CGCCTCTAGCGAGAGCTATG
cfa2155 5AL 55 F: TTTGTTACAACCCAGGGGG; R: TTGTGTGGCGAAAGAAACAG
cfd8 5DS 60 F: ACCACCGTCATGTCACTGAG; R: GTGAAGACGACAAGACGCAA
gwml69 6AL 55 F: ACCACTGCAGAGAACACATACG; R: GTGCTCTGCTCTAAGTGTGGG
barc345 6BL 55 F: CGCCAGACTGCTAGGATAATACTTT; R: GCGGCTAGTGCTCCCTCATAAT
barcl121 6DL 60 F: GCGAGCAAACTGATCCCAAAAAG; R: TATCGGTGAGTACGCCAAAAACA
cfa2123 7AS 60 F: CGGTCTTTGTTTGCTCTAAACC; R: ACCGGCCATCTATGATGAAG
wmc476 7BS 55 F: TACCAACCACACCTGCGAGT; R: CTAGATGAACCTTCGTGCGG
gwm44 7DS 65 F: GTTGAGCTTTTCAGTTCGGC; R: ACTGGCATCCACTGAGCTG

图1

野生型与突变体RL1的表型鉴定 a、b: 分别代表WT与RL1的抽穗期、苗期表型; a中, 标尺为20 cm; b中, 标尺为10 cm。c: 野生型与RL1不同时期卷曲程度的比较, 左为野生型, 右为RL1, 标尺为1 cm。"

图2

野生型与突变体RL1的株型比较 a: WT与RL1的茎秆, 标尺为 20 cm; b、c: 成熟期WT与RL1穗长及各节间长(I、II、III、IV), 标尺为10 cm; *: 在P < 0.05区间差异显著, **: 在P < 0.01差异极显著。"

表2

野生型与突变体RL1的主要农艺性状比较"

性状Trait 种子萌发15 d地上部鲜重
Aboveground fresh weight at 15 days of germination (g)
种子萌发15 d地下部鲜重
Subsurface fresh weight at 15 days of germination (g)
种子萌发15 d
根数目
Root number at 15 days of germination
种子萌发15 d
最大根长
Maximum root length at 15 days of germination (cm)
抽穗期
Heading stage (d)
成熟期
Maturity stage (d)
株高
Plant height
(cm)
旗叶面积
Flag leaf area (cm2)
旗叶长
Flag leaf length (cm)
旗叶宽
Flag leaf width (cm)
穗粒数
Grain number per spike
小穗数
Spikelet number
千粒重
1000-grain weight (g)
WT 0.22±0.01** 0.08±0.01 7±1.3 8.13±0.84 199±1 248±1 78.00±0.28** 24.62±5.14 21.02±2.65 1.51±0.12** 56.75±6.65** 19.25±1.25 52.25±0.91**
RL1 0.14±0.00 0.08±0.01 7±1.5 8.08±1.26 199±1 247±1 67.67±2.19 19.72±2.51 23.4±2.45 1.09±0.02 35.5±1.91 19.00±0.81 33.70±0.21

图3

野生型与突变体RL1成熟籽粒的TTC染色 a: 种胚着色图, 标尺为2 mm; b、c: 种胚放大图, 标尺为200 μm。"

图4

野生型与突变体RL1的光合参数与SPAD的分析 a: 蒸腾速率; b: 气孔导度; c: 净光合速率; d: 细胞间隙CO2浓度; e: 叶绿素含量; f: 水分利用率。**: P < 0.01差异极显著。"

图5

叶片横切面石蜡切片分析 a: WT和RL1的旗叶横切图, 标尺为1000 μm; b、c: 为a图的放大图, 标尺为 500 μm; d、e: 分别为b、c图的放大图, 标尺为200 μm; f: 两维管束之间的泡状细胞的数量和面积。SC: 厚壁细胞; PC: 薄壁细胞; BC: 泡状细胞; LV: 大叶脉; SV: 小叶脉; ad: 近轴面; ab: 远轴面。**: 在0.01概率水平上差异显著。"

附表2

RL1与晋麦47/临汾5064正反交F1"

杂交组合
Cross combination
F1表型及卷曲指数
Phenotype of F1 and leaf rolled index
F1株数
Number of plants in F1
RL1×晋麦47 RL1/Jinmai 47 微卷(抽穗期LRIs: 0.64-0.76) Slightly curl (Heading date LRIs: 0.64-0.76) 17
晋麦47×RL1 Jinmai 47/RL1 微卷(抽穗期LRIs: 0.66-0.78) Slightly curl (Heading date LRIs: 0.66-0.78) 18
RL1×临汾5064 RL1/Linfen 5064 微卷(抽穗期LRIs: 0.61-0.76) Slightly curl (Heading date LRIs: 0.61-0.76) 17
临汾5064×RL1 Linfen 5064/RL1 微卷(抽穗期LRIs: 0.68-0.80) Slightly curl (Heading date LRIs: 0.68-0.80) 18

表3

F2代群体材料表型分离统计"

杂交组合
Cross combination
总株数
Number of plants
平展叶
Spread leaf
轻微卷叶
Slightly coiled leaf
高度卷叶
Highly rolled leaf
理论比例
Ratio of theory
卡方
χ2
RL1/晋麦47 RL1/Jinmai 47 176 45 94 37 1:2:1 0.03
RL1/临汾5064 RL1/Linfen 5064 173 44 95 34 1:2:1 0.01

图6

RL1的精细定位"

表4

水稻叶片卷曲相关基因在小麦中的同源基因"

水稻基因
Rice gene
基因注释
Gene annotation
部分同源群
Homoeologous groups
小麦的同源基因
Wheat gene
OsACL1 Os04g33860 2 TraesCS2A01G296600 TraesCS2B01G312800 TraesCS2D01G294500
OsDEK1 Os02g47970 6 TraesCS6A01G275500 TraesCS6B01G302900 TraesCS6D01G255800
OsCFL1 Os02g31140 4 TraesCS4A01G407300 TraesCS4B01G306500 TraesCS4D01G304700
OsMYB103L Os08g05520 7 TraesCS7A01G304500 TraesCS7B01G204800 TraesCS7D01G300000
OsVIL3 Os02g05840 6 TraesCS6A02G123400 TraesCS6B02G151600 TraesCS6D02G113600
OsAGO7 Os03g33650 2 TraesCS2A01G414800 TraesCS2B01G434000 TraesCS2D01G412100
OsCOW1 Os03g06654 4 TraesCS4A01G027500 TraesCS4B01G278300 TraesCS4D01G276600
OsCSLD4 Os12g36890 5 TraesCS5A01G090500 TraesCS5B01G096200 TraesCS5D01G102600
OsHOX32 Os03g43930 5 TraesCS5A01G375800 TraesCS5B01G378000 TraesCS5D01G385300
OsYAB1 Os07g06620 5 TraesCS5A01G371500 TraesCS5B01G373600 TraesCS5D01G380900
OsZHD1 Os09g29130 5 TraesCS5A01G246500 TraesCS5B01G243800 TraesCS5D01G253100
OsPSL1 Os01g19170 1 TraesCS1A01G311100 TraesCS1B01G322500 TraesCS1D01G311000
OsREL1 Os01g64380 2 TraesCS2A01G065100 TraesCS2B01G077300 TraesCS2D01G063200
OsREL2 Os10g41310 1 TraesCS1A01G218200 TraesCS1B01G231600 TraesCS1D01G219800
Osrl14 Os10g40960 1 TraesCS1A01G221200 TraesCS1B01G234500 TraesCS1D01G222800
OsROC5 Os02g45250 6 TraesCS6A01G255800 TraesCS6B01G269700 TraesCS6D01G237000
OsRoc8 Os06g10600 6 TraesCS6A01G324500 TraesCS6B01G354900 TraesCS6D01G304300
OsSLL1 Os09g23200 5 TraesCS5A01G203200 TraesCS5B01G201900 TraesCS5D01G209600
OsSRL2 Os03g19520 4 TraesCS4A01G121600 TraesCS4B01G181700 TraesCS4D01G184300
OsSrl1 Os07g01240 2 TraesCS2A01G256400 TraesCS2B01G286100 TraesCS2D01G347200
OsOFP1 Os01g12690 3 TraesCS3A01G151800 TraesCS3B01G178800 TraesCS3D01G159700
OsMKB3 Os03g52320 4 TraesCS4A01G250600 TraesCS4B01G064000 TraesCS4D01G062900
OsLBD3-7 Os03g57670 5 TraesCS5A01G515300 TraesCS5B01G282700 TraesCS5D01G291300
OsARVL4 Os04g33580 1 TraesCS1A01G036100 TraesCS1B01G231600 TraesCS1D01G219800
OsARF18 Os06g47150 7 TraesCS7A01G446900 TraesCS7B01G346700 TraesCS7D01G436800
OsWOX3A Os12g01120 5 TraesCS5A01G157300 TraesCS5B01G156400 TraesCS5D01G162600
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