园艺学报 ›› 2023, Vol. 50 ›› Issue (9): 1867-1888.doi: 10.16420/j.issn.0513-353x.2022-0681
收稿日期:
2023-04-03
修回日期:
2023-06-13
出版日期:
2023-09-25
发布日期:
2023-09-26
通讯作者:
基金资助:
LU Jing, WEI Suyun, YIN Tongming, CHEN Yingnan*()
Received:
2023-04-03
Revised:
2023-06-13
Published:
2023-09-25
Online:
2023-09-26
Contact:
*(E-mail:chenyingnan@njfu.edu.cn)
摘要:
Type-A response regulators(RR)是细胞分裂素信号转导的末端组分,仅具有REC接收域,不仅影响植物生长发育,还响应非生物胁迫。本文中详细梳理了近年来草本和木本植物type-A RR鉴定、进化关系、表达模式、功能特征等研究进展,总结了潜在的调控网络,以期为深入理解type-A RR负调节细胞分裂素信号的机制提供参考。
陆静, 韦素云, 尹佟明, 陈赢男. Type-A细胞分裂素响应调节因子基因家族研究进展[J]. 园艺学报, 2023, 50(9): 1867-1888.
LU Jing, WEI Suyun, YIN Tongming, CHEN Yingnan. Research Progress on the Cytokinin Type-A Response Regulator Gene Family[J]. Acta Horticulturae Sinica, 2023, 50(9): 1867-1888.
功能特征 Functional characteristics | 物种 Species | 基因名 Gene name | 亚细胞定位 Subcellular localization | 基因表达特性与表型 Gene expression characteristics and phenotype | 参考文献 Reference |
---|---|---|---|---|---|
根生长发育 Root development | 拟南芥 Arabidopsis thaliana | ARR5 | 细胞核 Nucleus | 在根顶端分生组织表达量较高 Highly expressed in the apical meristem of roots | To et al., |
ARR7 | 细胞核 Nucleus | 过表达株根长;arr7突变体根干细胞发育系统受损 The roots of overexpressing plants were longer;the arr7 mutant has a defective root stem-cell system | Dortay et al., | ||
ARR15 | 细胞核 Nucleus | 在根维管形成层中表达 Expressed in root vascular cambium Arr15突变体根干细胞发育系统受损 The arr15 mutant has a defective root stem-cell system | Kiba et al., | ||
ARR16 | 细胞质 Cytoplasm | 在根内皮层表达 Expressed in root endodermis Arr16/17突变体根尖失去向水性 The root tips of arr16/17 mutant lost hydrotropism | Kiba et al., | ||
ARR17 | - | ||||
水稻 Oryza sativa | OsRR2 | - | 在WOX11突变水稻表达上调;在WOX11过表达植株表达下调; 在ren1-D显性突变体水稻表达下调 Upregulated in WOX11 mutant rice plants;downregulated in WOX11 overexpressing plants; downregulated in ren1-D dominant mutant | Zhao et al., Gao et al., | |
OsRR6 | - | 过表达根系发育不良,不定根数量改变 The overexpressing plants caused defects in the root system and altered adventitious root numbers | Bhaskar et al., | ||
番茄 Solanum lycopersicum | SIRR4 | - | 仅在侧根中特异表达 Specifically expressed in lateral roots | Gupta et al., | |
大豆 Gylcine max | GmRR06 | - | 在根中表达量最高 Highest expressed in roots | Le et al., | |
毛果杨 Populus trichocarpa | PtRR1 | 细胞核 Nucleus | 在根中表达 Expressed in roots | Ramírez-Carvajal et al., | |
下胚轴伸长 Hypocotyl elongation | 拟南芥 A. thaliana | ARR3 | 细胞核 Nucleus | arr3/4双突变体在黑暗中生物钟延长,在白光和光/暗周期中下胚轴长 The arr3/4 double mutant has a lengthened circadian in the absence of light,and longer hypocotyls in both white light and light/dark cycles | Salomé et al., |
ARR4 | 细胞质 Cytoplasm | ||||
水稻 O. sativa | OsRR6 | - | 过表达下胚轴生长受到抑制 The hypocotyl growth in overexpressing plants were inhibited | Bhaskar et al., | |
茎生长发育 Stem development | 拟南芥 A. thaliana | ARR4 | 细胞质 Cytoplasm | 在茎中高表达 Highly expressed in stems 过表达芽分化速度快 The overexpressing plants promoted shoot formation | Osakabe et al., |
ARR5 | 细胞核 Nucleus | 在茎部顶端分生组织中高表达 Highly expressed in the apical meristem of stems | D’ Agostino et al., | ||
ARR7 | 细胞核 Nucleus | arr7突变体茎尖分生组织发育快 The arr7 mutants have faster development of shoot apical meristem | Zhao et al., | ||
ARR8 | 细胞核 Nucleus | 过表达芽分化慢 The overexpressing plants inhibited shoot formation | Dortay et al., | ||
ARR15 | 细胞核 Nucleus | arr15突变体茎尖分生组织发育快 the arr15 mutants have faster development of apical meristem of stems | Zhao et al., | ||
水稻 O. sativa | OsRR5 | - | 在SL相关d53突变体茎中高表达 High expressed in stem of SL-related d53 mutant | Duan et al., | |
番茄 S. lycopersicum | SIRR4 | - | 在番茄茎尖分生组织中高表达 Expressed in the apical meristem of stems in tomato | Shani et al., | |
叶生长发育 Leaf development | 拟南芥 A. thaliana | ARR16 | 细胞质 Cytoplasm | 过表达ARR16叶片黄化严重,气孔数量降低;arr16/17双突变体气孔数量增多 The overexpression of ARR16 caused severe leave senescence and stomas number reduction;the arr16/17 double mutants have more stomas | Dortay et al., |
ARR17 | - | ||||
水稻 O. sativa | OsRR6 | - | 过表达叶片持绿长,花青素积累 The overexpressing plants resulted in sustained green leaves and accumulation of anthocyanin in the leaves | Bhaskar et al., | |
OsRR9 | - | osrr9/10双突变体延缓叶片衰老 The osrr9/10 double mutant delayed leaf senescence | Wang et al., | ||
OsRR10 | - | ||||
玉米 Zea mays | ZmRR3 | 细胞质 Cytoplasm | Mu转座子插入突变改变叶序 Mutator insection caused opposite phyllotaxy | Asakura et al., | |
番茄 S. lycopersicum | SlRR4 | - | 在幼叶原基中高表达 Highly expressed in the young leave primordia | Shani et al., | |
SlRR7 | - | ||||
芽生长发育 Shoot development | 拟南芥 A. thaliana | ARR4 | 细胞核 Nucleus | 过表达芽分化数量多 The overexpressing plants increased the number of shoot formation | Osakabe et al., |
ARR8 | 细胞核 Nucleus | 过表达芽分化少 The overexpressing plants decreased the number of shoot formation | Osakabe et al., | ||
ARR15 | 细胞核 Nucleus | 过表达愈伤组织少,芽分化少 The overexpressing plants decreased the formation of callus and shoot | Kiba et al., | ||
大豆 Glycine max | GmRR11 | - | Mochida et al., | ||
苹果 Malus × domestica | MdRR9 | - | 过表达腋芽和分枝数量显著增加。 The overexpressing plants have more axillary buds and branches | 陈皓, | |
海岸松 Pinus pinaster | PipsRRA1 | - | 在不定芽中高表达 High expressed in adventitious callogenesis | Alvarez et al., | |
花发育 Flower development | 拟南芥 A. thaliana | ARR7 | 细胞核 Nucleus | 过表达导致花发育异常 The overexpressing plants caused defective flower development | Dortay et al., |
ARR16 | 细胞质 Nucleus | 在雌核发育的7、8、9和12阶段表达 Expressed during gynoecia development at stage 7,8,9,12 | Dortay et al., | ||
水稻 O. sativa | OsRR1 | - | 过表达花期长 The overexpressing plants have a longer flowering time | Cho et al., | |
OsRR6 | - | 过表达圆锥花序发育不良 The overexpressing plants have defective panicle development | Hirose et al., | ||
OsRR9 | - | Osrr9/10双突变体小穗数减少 The number of spikelets in osrr9/10 double mutants was reduced | Wang et al., | ||
OsRR10 | - | ||||
玉米 Z. mays | ZmRR1 ~ ZmRR2 | 细胞质 Cytoplasm | 在雄花序中表达 Expressed in tassels | Asakura et al., | |
ZmRR3 | 细胞质 Cytoplasm | 在雌花序中表达 Expressed in ears | Asakura et al., | ||
香脂杨 P. balsamifera | PbRR9 | - | 仅有的性别特异性甲基化基因 Only sex-specific methylation gene | Bräutigam et al., | |
毛果杨 P. trichocarpa | ARR17 | - | Müller et al., | ||
欧洲山杨 P. tremula | ARR17 | - | 敲除导致雌株开雄花 Knockout resulted in the production of male flowers in female plants | Müller et al., | |
美洲黑杨 P. deltoides | FERR | 细胞质 Cytoplasm | 仅在雌花原基中高表达 Highly expressed in female flower primordia 过表达促进雌蕊发育 The overexpressing plants promoted carpel development | Xue et al., | |
红皮柳 Salix purpurea | GATA15 | - | 在含有雌花原基的茎尖中特异表达 Specifically expressed in shoot tips containing floral primordia | Hyden et al., | |
SpRR9 | - | 在雌株葇夷花序中高表达 Highly expressed in female catkins | Zhou et al., | ||
果实生长发育 Fruit development | 番茄 S. lycopersicum | SlRR1 | - | 在果实发育IG2阶段高表达,在成熟阶段低表达 Highly expressed during fruit developmental stage IG2,and down-regulated during ripening phase | Bianchetti et al., |
SlRR3 | - | ||||
SlRR4 | - | ||||
SlRR7 | - | ||||
苹果 M. domestica | MdRR5 | - | 在果实脱落前乙烯增加时表达下降 Expression decreased when ethylene increased before fruit shedding | Cin et al., | |
种子生长发育 Seed development | 玉米 Z. mays | ZmTCRR-1 | 细胞质 Cytoplasm | 在未成熟胚乳转移细胞层中特异表达 Specifically expressed in the immature endosperm transfer-cell layer | Asakura et al., |
小麦 Triticum aestivum | TaARR9 | - | 在种子中特异性表达 Specifically expressed in wheat seeds | Tuan et al., | |
非生物胁迫敏感性 Sensitivity to abiotic stress | 拟南芥 A. thaliana | ARR5 | 细胞核 Nucleus | 过表达耐寒 The overexpressing plants increased freezing tolerance. | Dortay et al., |
ARR6 | 细胞核 Nucleus | 下调可以提高对氧化应激的耐受性。 Downregulation can enhance the tolerance to oxidative stress | Dortay et al., | ||
ARR7 | 细胞核 Nucleus | 过表达耐寒 The overexpressing plants increased freezing tolerance | Dortay et al., | ||
ARR15 | 细胞核 Nucleus | 过表达耐寒 The overexpressing plants increased freezing tolerance | Dortay et al., | ||
水稻 O. sativa | OsRR6 | - | 过表达在NaCl和甘露醇种子萌发处理下率高 The overexpressing plants have higher seed germination rates with the respective treatment of NaCl and mannitol treatment | Bhaskar et al., | |
OsRR9 | - | 在47 ℃高温下表达上调 Up-regulated at a high temperature of 47 ℃ osrr9/osrr10双突变体在盐胁迫下叶片不易蜷缩 osrr9/osrr10 double mutants reduced leaf curling under salinity stress | Wang et al., | ||
OsRR10 | - | 在渗透胁迫和盐胁迫下均表达下调 Down-regulated under osmotic stress and salinity stress | Wang et al., | ||
玉米 Z.mays | ZmRR1 | 细胞质 Cytoplasm | 在低温处理下,过表达植抗性强,而突变体抗性差 The overexpressing plants exhibited strong resistance while the mutants showed weak resistance under low-temperature treatment | Asakura et al., | |
白菜 Brassica rapa | BrRR1 | - | 在盐胁迫处理下,BrRR19基因表达上调;在ABA处理下,BrRR3和BrRR17表达下调;在反式玉米素处理下BrRR1/3/7/8/12/17/19表达上调;在根瘤感染初期BrRR1/6表达上调、在根瘤扩张期,BrRR4表达上调 BrRR19 was upregulated under salt stress;while BrRR3 and BrRR17 were downregulated under ABA treatment;BrRR1/3/7/8/12/17/19 were upregulated under t-zeatin treatment;BrRR1/6 were upregulated during the primary phase of clubroot infection,while BrRR4 was upregulated during the gall enlargement phase | Liu et al., | |
BrRR3 | - | ||||
BrRR4 | - | ||||
BrRR6 | - | ||||
BrRR7 | - | ||||
BrRR8 | - | ||||
BrRR12 | - | ||||
BrRR17 | - | ||||
BrRR19 | - | ||||
番茄 S. lycopersicum | SIRR5 | - | 在抗晚疫病的番茄中表达下调,而在晚疫病敏感的番茄中上调Down-regulated in resistant tomato,while up-regulated in sensitive tomato | Cui et al., | |
百脉根 Lotus japonicus | LjaRRa1 ~ LjaRRa6 | - | 在反式玉米素处理后表达上调 Up-regulated after t-zeatin treatment | Ishida et al., | |
苹果 M. domestica | MdRR3 | - | 在6-BA处理后表达上调 Up-regulated after 6-BA treatment | Li et al., | |
MdRR14 | - | ||||
银灰杨 P. × canescens | PtaRR3 | - | 干旱胁迫下在杨树的茎的初生木质部中表达下调 Down-regulated in the primary xylem of poplar stems under drought stress | Paul et al., |
表1 Type-A RR基因在不同植物不同生长发育阶段及非生物胁迫下功能特征
Table 1 Functional characteristics of type-A RR in different growth and development stages of different plants and under abiotic stresses
功能特征 Functional characteristics | 物种 Species | 基因名 Gene name | 亚细胞定位 Subcellular localization | 基因表达特性与表型 Gene expression characteristics and phenotype | 参考文献 Reference |
---|---|---|---|---|---|
根生长发育 Root development | 拟南芥 Arabidopsis thaliana | ARR5 | 细胞核 Nucleus | 在根顶端分生组织表达量较高 Highly expressed in the apical meristem of roots | To et al., |
ARR7 | 细胞核 Nucleus | 过表达株根长;arr7突变体根干细胞发育系统受损 The roots of overexpressing plants were longer;the arr7 mutant has a defective root stem-cell system | Dortay et al., | ||
ARR15 | 细胞核 Nucleus | 在根维管形成层中表达 Expressed in root vascular cambium Arr15突变体根干细胞发育系统受损 The arr15 mutant has a defective root stem-cell system | Kiba et al., | ||
ARR16 | 细胞质 Cytoplasm | 在根内皮层表达 Expressed in root endodermis Arr16/17突变体根尖失去向水性 The root tips of arr16/17 mutant lost hydrotropism | Kiba et al., | ||
ARR17 | - | ||||
水稻 Oryza sativa | OsRR2 | - | 在WOX11突变水稻表达上调;在WOX11过表达植株表达下调; 在ren1-D显性突变体水稻表达下调 Upregulated in WOX11 mutant rice plants;downregulated in WOX11 overexpressing plants; downregulated in ren1-D dominant mutant | Zhao et al., Gao et al., | |
OsRR6 | - | 过表达根系发育不良,不定根数量改变 The overexpressing plants caused defects in the root system and altered adventitious root numbers | Bhaskar et al., | ||
番茄 Solanum lycopersicum | SIRR4 | - | 仅在侧根中特异表达 Specifically expressed in lateral roots | Gupta et al., | |
大豆 Gylcine max | GmRR06 | - | 在根中表达量最高 Highest expressed in roots | Le et al., | |
毛果杨 Populus trichocarpa | PtRR1 | 细胞核 Nucleus | 在根中表达 Expressed in roots | Ramírez-Carvajal et al., | |
下胚轴伸长 Hypocotyl elongation | 拟南芥 A. thaliana | ARR3 | 细胞核 Nucleus | arr3/4双突变体在黑暗中生物钟延长,在白光和光/暗周期中下胚轴长 The arr3/4 double mutant has a lengthened circadian in the absence of light,and longer hypocotyls in both white light and light/dark cycles | Salomé et al., |
ARR4 | 细胞质 Cytoplasm | ||||
水稻 O. sativa | OsRR6 | - | 过表达下胚轴生长受到抑制 The hypocotyl growth in overexpressing plants were inhibited | Bhaskar et al., | |
茎生长发育 Stem development | 拟南芥 A. thaliana | ARR4 | 细胞质 Cytoplasm | 在茎中高表达 Highly expressed in stems 过表达芽分化速度快 The overexpressing plants promoted shoot formation | Osakabe et al., |
ARR5 | 细胞核 Nucleus | 在茎部顶端分生组织中高表达 Highly expressed in the apical meristem of stems | D’ Agostino et al., | ||
ARR7 | 细胞核 Nucleus | arr7突变体茎尖分生组织发育快 The arr7 mutants have faster development of shoot apical meristem | Zhao et al., | ||
ARR8 | 细胞核 Nucleus | 过表达芽分化慢 The overexpressing plants inhibited shoot formation | Dortay et al., | ||
ARR15 | 细胞核 Nucleus | arr15突变体茎尖分生组织发育快 the arr15 mutants have faster development of apical meristem of stems | Zhao et al., | ||
水稻 O. sativa | OsRR5 | - | 在SL相关d53突变体茎中高表达 High expressed in stem of SL-related d53 mutant | Duan et al., | |
番茄 S. lycopersicum | SIRR4 | - | 在番茄茎尖分生组织中高表达 Expressed in the apical meristem of stems in tomato | Shani et al., | |
叶生长发育 Leaf development | 拟南芥 A. thaliana | ARR16 | 细胞质 Cytoplasm | 过表达ARR16叶片黄化严重,气孔数量降低;arr16/17双突变体气孔数量增多 The overexpression of ARR16 caused severe leave senescence and stomas number reduction;the arr16/17 double mutants have more stomas | Dortay et al., |
ARR17 | - | ||||
水稻 O. sativa | OsRR6 | - | 过表达叶片持绿长,花青素积累 The overexpressing plants resulted in sustained green leaves and accumulation of anthocyanin in the leaves | Bhaskar et al., | |
OsRR9 | - | osrr9/10双突变体延缓叶片衰老 The osrr9/10 double mutant delayed leaf senescence | Wang et al., | ||
OsRR10 | - | ||||
玉米 Zea mays | ZmRR3 | 细胞质 Cytoplasm | Mu转座子插入突变改变叶序 Mutator insection caused opposite phyllotaxy | Asakura et al., | |
番茄 S. lycopersicum | SlRR4 | - | 在幼叶原基中高表达 Highly expressed in the young leave primordia | Shani et al., | |
SlRR7 | - | ||||
芽生长发育 Shoot development | 拟南芥 A. thaliana | ARR4 | 细胞核 Nucleus | 过表达芽分化数量多 The overexpressing plants increased the number of shoot formation | Osakabe et al., |
ARR8 | 细胞核 Nucleus | 过表达芽分化少 The overexpressing plants decreased the number of shoot formation | Osakabe et al., | ||
ARR15 | 细胞核 Nucleus | 过表达愈伤组织少,芽分化少 The overexpressing plants decreased the formation of callus and shoot | Kiba et al., | ||
大豆 Glycine max | GmRR11 | - | Mochida et al., | ||
苹果 Malus × domestica | MdRR9 | - | 过表达腋芽和分枝数量显著增加。 The overexpressing plants have more axillary buds and branches | 陈皓, | |
海岸松 Pinus pinaster | PipsRRA1 | - | 在不定芽中高表达 High expressed in adventitious callogenesis | Alvarez et al., | |
花发育 Flower development | 拟南芥 A. thaliana | ARR7 | 细胞核 Nucleus | 过表达导致花发育异常 The overexpressing plants caused defective flower development | Dortay et al., |
ARR16 | 细胞质 Nucleus | 在雌核发育的7、8、9和12阶段表达 Expressed during gynoecia development at stage 7,8,9,12 | Dortay et al., | ||
水稻 O. sativa | OsRR1 | - | 过表达花期长 The overexpressing plants have a longer flowering time | Cho et al., | |
OsRR6 | - | 过表达圆锥花序发育不良 The overexpressing plants have defective panicle development | Hirose et al., | ||
OsRR9 | - | Osrr9/10双突变体小穗数减少 The number of spikelets in osrr9/10 double mutants was reduced | Wang et al., | ||
OsRR10 | - | ||||
玉米 Z. mays | ZmRR1 ~ ZmRR2 | 细胞质 Cytoplasm | 在雄花序中表达 Expressed in tassels | Asakura et al., | |
ZmRR3 | 细胞质 Cytoplasm | 在雌花序中表达 Expressed in ears | Asakura et al., | ||
香脂杨 P. balsamifera | PbRR9 | - | 仅有的性别特异性甲基化基因 Only sex-specific methylation gene | Bräutigam et al., | |
毛果杨 P. trichocarpa | ARR17 | - | Müller et al., | ||
欧洲山杨 P. tremula | ARR17 | - | 敲除导致雌株开雄花 Knockout resulted in the production of male flowers in female plants | Müller et al., | |
美洲黑杨 P. deltoides | FERR | 细胞质 Cytoplasm | 仅在雌花原基中高表达 Highly expressed in female flower primordia 过表达促进雌蕊发育 The overexpressing plants promoted carpel development | Xue et al., | |
红皮柳 Salix purpurea | GATA15 | - | 在含有雌花原基的茎尖中特异表达 Specifically expressed in shoot tips containing floral primordia | Hyden et al., | |
SpRR9 | - | 在雌株葇夷花序中高表达 Highly expressed in female catkins | Zhou et al., | ||
果实生长发育 Fruit development | 番茄 S. lycopersicum | SlRR1 | - | 在果实发育IG2阶段高表达,在成熟阶段低表达 Highly expressed during fruit developmental stage IG2,and down-regulated during ripening phase | Bianchetti et al., |
SlRR3 | - | ||||
SlRR4 | - | ||||
SlRR7 | - | ||||
苹果 M. domestica | MdRR5 | - | 在果实脱落前乙烯增加时表达下降 Expression decreased when ethylene increased before fruit shedding | Cin et al., | |
种子生长发育 Seed development | 玉米 Z. mays | ZmTCRR-1 | 细胞质 Cytoplasm | 在未成熟胚乳转移细胞层中特异表达 Specifically expressed in the immature endosperm transfer-cell layer | Asakura et al., |
小麦 Triticum aestivum | TaARR9 | - | 在种子中特异性表达 Specifically expressed in wheat seeds | Tuan et al., | |
非生物胁迫敏感性 Sensitivity to abiotic stress | 拟南芥 A. thaliana | ARR5 | 细胞核 Nucleus | 过表达耐寒 The overexpressing plants increased freezing tolerance. | Dortay et al., |
ARR6 | 细胞核 Nucleus | 下调可以提高对氧化应激的耐受性。 Downregulation can enhance the tolerance to oxidative stress | Dortay et al., | ||
ARR7 | 细胞核 Nucleus | 过表达耐寒 The overexpressing plants increased freezing tolerance | Dortay et al., | ||
ARR15 | 细胞核 Nucleus | 过表达耐寒 The overexpressing plants increased freezing tolerance | Dortay et al., | ||
水稻 O. sativa | OsRR6 | - | 过表达在NaCl和甘露醇种子萌发处理下率高 The overexpressing plants have higher seed germination rates with the respective treatment of NaCl and mannitol treatment | Bhaskar et al., | |
OsRR9 | - | 在47 ℃高温下表达上调 Up-regulated at a high temperature of 47 ℃ osrr9/osrr10双突变体在盐胁迫下叶片不易蜷缩 osrr9/osrr10 double mutants reduced leaf curling under salinity stress | Wang et al., | ||
OsRR10 | - | 在渗透胁迫和盐胁迫下均表达下调 Down-regulated under osmotic stress and salinity stress | Wang et al., | ||
玉米 Z.mays | ZmRR1 | 细胞质 Cytoplasm | 在低温处理下,过表达植抗性强,而突变体抗性差 The overexpressing plants exhibited strong resistance while the mutants showed weak resistance under low-temperature treatment | Asakura et al., | |
白菜 Brassica rapa | BrRR1 | - | 在盐胁迫处理下,BrRR19基因表达上调;在ABA处理下,BrRR3和BrRR17表达下调;在反式玉米素处理下BrRR1/3/7/8/12/17/19表达上调;在根瘤感染初期BrRR1/6表达上调、在根瘤扩张期,BrRR4表达上调 BrRR19 was upregulated under salt stress;while BrRR3 and BrRR17 were downregulated under ABA treatment;BrRR1/3/7/8/12/17/19 were upregulated under t-zeatin treatment;BrRR1/6 were upregulated during the primary phase of clubroot infection,while BrRR4 was upregulated during the gall enlargement phase | Liu et al., | |
BrRR3 | - | ||||
BrRR4 | - | ||||
BrRR6 | - | ||||
BrRR7 | - | ||||
BrRR8 | - | ||||
BrRR12 | - | ||||
BrRR17 | - | ||||
BrRR19 | - | ||||
番茄 S. lycopersicum | SIRR5 | - | 在抗晚疫病的番茄中表达下调,而在晚疫病敏感的番茄中上调Down-regulated in resistant tomato,while up-regulated in sensitive tomato | Cui et al., | |
百脉根 Lotus japonicus | LjaRRa1 ~ LjaRRa6 | - | 在反式玉米素处理后表达上调 Up-regulated after t-zeatin treatment | Ishida et al., | |
苹果 M. domestica | MdRR3 | - | 在6-BA处理后表达上调 Up-regulated after 6-BA treatment | Li et al., | |
MdRR14 | - | ||||
银灰杨 P. × canescens | PtaRR3 | - | 干旱胁迫下在杨树的茎的初生木质部中表达下调 Down-regulated in the primary xylem of poplar stems under drought stress | Paul et al., |
图1 本文中涉及的type-A RR基因谱系树 At:拟南芥;Os:水稻;Zm:玉米;Br:白菜;Lja:百脉根;Ta:小麦;Sl:番茄;Gm:大豆;Md:苹果;Pt:毛果杨;Pb:香脂杨;Pta:银灰杨;Pd:美洲黑杨;Sp:红皮柳;Pips:海岸松。
Fig. 1 The phylogenetic tree of type-A RR mentioned in this review At:Arabidopsis thaliana;Os:Oryza sativa;Zm:Zea mays;Br:Brassica rapa;Lja:Lotus japonicus;Ta:Triticum aestivum; Sl:Solanum lycopersicum;Gm:Gylcine max;Pt:Populus trichocarpa;Pta:P. × canescens;Pd:P. deltoides;Sp:Salix purpurea;Pips:Pinus pinea.
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