Chinese Bulletin of Botany ›› 2024, Vol. 59 ›› Issue (1): 110-121.DOI: 10.11983/CBB23029
• SPECIAL TOPICS • Previous Articles Next Articles
Zhiye Du1, Mingyu Li1, Ji Chen2, Jin Huang1,*()
Received:
2023-03-03
Accepted:
2023-05-31
Online:
2024-01-01
Published:
2023-05-31
Contact:
*E-mail: Zhiye Du, Mingyu Li, Ji Chen, Jin Huang. Research Advances in Plant Stress Associated Protein Functions[J]. Chinese Bulletin of Botany, 2024, 59(1): 110-121.
Figure 2 Hypothetical model of plant stress associated proteins (SAPs) participating in ubiquitination pathway Ub: Ubiquitin; TF: Transcription factor; RAD23: A shuttle factor that can act as ubiquitin receptor. The solid and dashed lines indicate the known and unknown pathway, respectively. Plant SAPs may participate in K48-linked polyubiquitination and K63-linked polyubiquitination as E3 ubiquitin ligases. They may mediate the degradation of substrate proteins through K48-linked polyubiquitination, and regulate downstream signal transduction through K63-linked polyubiquitination. Plant SAPs may also interact with shuttle factors or components of the 26S proteasome, thus participating in the binding process of substrate proteins to the 26S proteasome.
Figure 3 Hypothetical model of plant stress associated proteins (SAPs) participating in signal transduction as redox sensors During changes in redox status, plant SAPs form dimers or oligomers through ZnF-A20 domain and ZnF-AN1 domain, then these complexes interact with receptor-like cytoplasmic kinase (RLCK). The regions between the zinc finger domains undergo conformational changes, and the cysteine in them mediates the redox information to RLCK, thus activating the downstream signal pathway.
Figure 4 Hypothetical model of plant stress associated proteins (SAPs) as transcription factors regulating downstream gene expression The arrows and T symbols in the nucleus indicate positive and negative regulation, respectively. The solid and dashed lines indicate the known and unknown function, respectively. Plant SAPs interact with nuclear proteins or are phosphorylated by protein kinases to enter the nucleus, where they regulate the expression of downstream genes through direct or indirect mechanisms.
基因 | 基因来源 | 转基因植物 | 功能 | 参考文献 |
---|---|---|---|---|
OsSAP1 | 水稻(Oryza sativa) | 烟草(Nicotiana tabacum) | 盐、冷和干旱胁迫耐受 | Mukhopadhyay et al., |
OsSAP4/ZFP185 | 水稻(O. sativa) | 盐、冷和干旱胁迫敏感 | Zhang et al., | |
OsSAP5 | 拟南芥(A. thaliana) | 热胁迫耐受 | Chen et al., | |
OsSAP6 | 水稻(O. sativa) | 苏打盐碱胁迫耐受 | Zhu et al., | |
OsSAP7 | 拟南芥(A. thaliana) | 干旱胁迫敏感 | Sharma et al., | |
OsSAP8 | 烟草(N. tabacum) 水稻(O. sativa) | 盐、冷和干旱胁迫耐受 | Kanneganti and Gupta, | |
OsSAP9/ZFP177 | 烟草(N. tabacum) | 冷、热和H2O2胁迫耐受, 盐和干旱胁迫敏感 | Huang et al., | |
OsSAP11 | 拟南芥(A. thaliana) | 盐和干旱胁迫耐受 | Giri et al., | |
OsSAP16 | 水稻(O. sativa) | 冷胁迫耐受 | Wang et al., | |
TaSAP5 | 小麦(Triticum aestivum) | 拟南芥(A. thaliana) 小麦(T. aestivum) | 干旱胁迫耐受 | Zhang et al., |
TaSAP7-A | 拟南芥(A. thaliana) | 盐和渗透胁迫敏感 | Li et al., | |
TaSAP12-D | 拟南芥(A. thaliana) | 盐胁迫耐受 | 王亦学等, | |
TaSAP17-D | 拟南芥(A. thaliana) | 盐胁迫耐受 | Xu et al., | |
AtSAP5 | 拟南芥(Arabidopsis thaliana) | 拟南芥(A. thaliana) | 盐、渗透和干旱胁迫耐受 | Kang et al., |
AtSAP9 | 拟南芥(A. thaliana) | 干旱胁迫耐受 | Kang et al., | |
AtSAP10 | 拟南芥(A. thaliana) | 热和重金属(镍、锰和锌)胁迫耐受 | Dixit and Dhankher, | |
AtSAP13 | 拟南芥(A. thaliana) | 盐、干旱和重金属(锌、砷和镉)胁迫耐受 | Dixit et al., | |
ZmSAP8 | 玉米(Zea mays) | 拟南芥(A. thaliana) | 干旱胁迫耐受 | Su et al., |
ZmSAP10 | 拟南芥(A. thaliana) | 冷胁迫耐受 盐和干旱胁迫敏感 | Xuan et al., | |
CaSAP14 | 辣椒(Capsicum annuum) | 拟南芥(A. thaliana) | 盐、干旱和渗透胁迫耐受 | Bae et al., |
GmSAP16 | 大豆(Glycine max) | 拟南芥(A. thaliana) 大豆(G. max) | 盐和干旱胁迫耐受 | Zhang et al., |
MusaSAP1 | 香蕉(Musa nana) | 香蕉(M. nana) | 盐、干旱和氧化胁迫耐受 | Sreedharan et al., |
MtSAP1 | 蒺藜苜蓿(Medicago trancatula) | 烟草(N. tabacum) | 盐、寒冷和渗透胁迫耐受 | Charrier et al., |
SbSAP14 | 高粱(Sorghum bicolor) | 水稻(O. sativa) | 盐胁迫耐受 | Wang et al., |
PtSAP13 | 毛果杨(Populus trichocarpa) | 拟南芥(A. thaliana) | 盐胁迫耐受 | Li et al., |
LmSAP | 香雪球(Lobularia maritima) | 烟草(N. tabacum) | 盐和渗透胁迫耐受 | Ben Saad, |
AlSAP | 獐茅(Aeluropus littoralis) | 水稻(O. sativa) | 干旱胁迫耐受 | Ghneim-Herrera et al., |
PpSAP1 | 桃(Prunus persica) | 欧洲李(Pr. domestica) | 干旱胁迫耐受 | Lloret et al., |
MdSAP15 | 苹果(Malus domestica) | 拟南芥(A. thaliana) | 干旱和渗透胁迫耐受 | Dong et al., |
PagSAP1 | 杂交杨树(P. alba × P. glandulosa) | 杂交杨树(P. alba × P. glandulosa) | 盐胁迫敏感 | Yoon et al., |
GhSAP8 | 陆地棉(Gossypium hirsutem) | 拟南芥(A. thaliana) | 盐胁迫耐受 | 王亦学等, |
IbSAP16 | 甘薯(Ipomoea batatas) | 拟南芥(A. thaliana) | 盐胁迫耐受 | Xie et al., |
Table 1 Function of transgenic plants expressing SAP genes under abiotic stresses
基因 | 基因来源 | 转基因植物 | 功能 | 参考文献 |
---|---|---|---|---|
OsSAP1 | 水稻(Oryza sativa) | 烟草(Nicotiana tabacum) | 盐、冷和干旱胁迫耐受 | Mukhopadhyay et al., |
OsSAP4/ZFP185 | 水稻(O. sativa) | 盐、冷和干旱胁迫敏感 | Zhang et al., | |
OsSAP5 | 拟南芥(A. thaliana) | 热胁迫耐受 | Chen et al., | |
OsSAP6 | 水稻(O. sativa) | 苏打盐碱胁迫耐受 | Zhu et al., | |
OsSAP7 | 拟南芥(A. thaliana) | 干旱胁迫敏感 | Sharma et al., | |
OsSAP8 | 烟草(N. tabacum) 水稻(O. sativa) | 盐、冷和干旱胁迫耐受 | Kanneganti and Gupta, | |
OsSAP9/ZFP177 | 烟草(N. tabacum) | 冷、热和H2O2胁迫耐受, 盐和干旱胁迫敏感 | Huang et al., | |
OsSAP11 | 拟南芥(A. thaliana) | 盐和干旱胁迫耐受 | Giri et al., | |
OsSAP16 | 水稻(O. sativa) | 冷胁迫耐受 | Wang et al., | |
TaSAP5 | 小麦(Triticum aestivum) | 拟南芥(A. thaliana) 小麦(T. aestivum) | 干旱胁迫耐受 | Zhang et al., |
TaSAP7-A | 拟南芥(A. thaliana) | 盐和渗透胁迫敏感 | Li et al., | |
TaSAP12-D | 拟南芥(A. thaliana) | 盐胁迫耐受 | 王亦学等, | |
TaSAP17-D | 拟南芥(A. thaliana) | 盐胁迫耐受 | Xu et al., | |
AtSAP5 | 拟南芥(Arabidopsis thaliana) | 拟南芥(A. thaliana) | 盐、渗透和干旱胁迫耐受 | Kang et al., |
AtSAP9 | 拟南芥(A. thaliana) | 干旱胁迫耐受 | Kang et al., | |
AtSAP10 | 拟南芥(A. thaliana) | 热和重金属(镍、锰和锌)胁迫耐受 | Dixit and Dhankher, | |
AtSAP13 | 拟南芥(A. thaliana) | 盐、干旱和重金属(锌、砷和镉)胁迫耐受 | Dixit et al., | |
ZmSAP8 | 玉米(Zea mays) | 拟南芥(A. thaliana) | 干旱胁迫耐受 | Su et al., |
ZmSAP10 | 拟南芥(A. thaliana) | 冷胁迫耐受 盐和干旱胁迫敏感 | Xuan et al., | |
CaSAP14 | 辣椒(Capsicum annuum) | 拟南芥(A. thaliana) | 盐、干旱和渗透胁迫耐受 | Bae et al., |
GmSAP16 | 大豆(Glycine max) | 拟南芥(A. thaliana) 大豆(G. max) | 盐和干旱胁迫耐受 | Zhang et al., |
MusaSAP1 | 香蕉(Musa nana) | 香蕉(M. nana) | 盐、干旱和氧化胁迫耐受 | Sreedharan et al., |
MtSAP1 | 蒺藜苜蓿(Medicago trancatula) | 烟草(N. tabacum) | 盐、寒冷和渗透胁迫耐受 | Charrier et al., |
SbSAP14 | 高粱(Sorghum bicolor) | 水稻(O. sativa) | 盐胁迫耐受 | Wang et al., |
PtSAP13 | 毛果杨(Populus trichocarpa) | 拟南芥(A. thaliana) | 盐胁迫耐受 | Li et al., |
LmSAP | 香雪球(Lobularia maritima) | 烟草(N. tabacum) | 盐和渗透胁迫耐受 | Ben Saad, |
AlSAP | 獐茅(Aeluropus littoralis) | 水稻(O. sativa) | 干旱胁迫耐受 | Ghneim-Herrera et al., |
PpSAP1 | 桃(Prunus persica) | 欧洲李(Pr. domestica) | 干旱胁迫耐受 | Lloret et al., |
MdSAP15 | 苹果(Malus domestica) | 拟南芥(A. thaliana) | 干旱和渗透胁迫耐受 | Dong et al., |
PagSAP1 | 杂交杨树(P. alba × P. glandulosa) | 杂交杨树(P. alba × P. glandulosa) | 盐胁迫敏感 | Yoon et al., |
GhSAP8 | 陆地棉(Gossypium hirsutem) | 拟南芥(A. thaliana) | 盐胁迫耐受 | 王亦学等, |
IbSAP16 | 甘薯(Ipomoea batatas) | 拟南芥(A. thaliana) | 盐胁迫耐受 | Xie et al., |
基因 | 基因来源 | 转基因植物 | 功能 | 参考文献 |
---|---|---|---|---|
AtSAP5 | 拟南芥(Arabidopsis thaliana) | 拟南芥(A. thaliana) | 黄瓜花叶病毒(cucumber mosaic virus, CMV)抗性增强 | Chang et al., |
AtSAP9 | 拟南芥(A. thaliana) | 宿主/非宿主病原菌抗性减弱 | Kang et al., | |
SlSAP3 | 番茄(Solanum lycopersicum) | 番茄(S. lycopersicum) | 病原菌(Pst DC3000)抗性增强 | Liu et al., |
SlSAP4 | 番茄(S. lycopersicum) | 病原菌(Botrytis cinerea)抗性增强 | Liu et al., | |
Pha13 | 蝴蝶兰(Phalaenopsis aphrodite) | 拟南芥(A. thaliana) | 烟草脆裂病毒(tobacco rattle virus, TRV)、CMV及Pst DC3000抗性增强 | Chang et al., |
Table 2 Function of transgenic plants expressing SAP genes under biotic stresses
基因 | 基因来源 | 转基因植物 | 功能 | 参考文献 |
---|---|---|---|---|
AtSAP5 | 拟南芥(Arabidopsis thaliana) | 拟南芥(A. thaliana) | 黄瓜花叶病毒(cucumber mosaic virus, CMV)抗性增强 | Chang et al., |
AtSAP9 | 拟南芥(A. thaliana) | 宿主/非宿主病原菌抗性减弱 | Kang et al., | |
SlSAP3 | 番茄(Solanum lycopersicum) | 番茄(S. lycopersicum) | 病原菌(Pst DC3000)抗性增强 | Liu et al., |
SlSAP4 | 番茄(S. lycopersicum) | 病原菌(Botrytis cinerea)抗性增强 | Liu et al., | |
Pha13 | 蝴蝶兰(Phalaenopsis aphrodite) | 拟南芥(A. thaliana) | 烟草脆裂病毒(tobacco rattle virus, TRV)、CMV及Pst DC3000抗性增强 | Chang et al., |
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