生物技术通报 ›› 2022, Vol. 38 ›› Issue (1): 1-14.doi: 10.13560/j.cnki.biotech.bull.1985.2021-1326
• 特约综述 • 下一篇
收稿日期:
2021-10-21
出版日期:
2022-01-26
发布日期:
2022-02-22
作者简介:
朱琳,硕士研究生,研究方向:植物发育遗传;E-mail: 基金资助:
ZHU Lin(), XIAN Feng-jun, ZHANG Qian-nan, HU Jun()
Received:
2021-10-21
Published:
2022-01-26
Online:
2022-02-22
摘要:
RNA编辑,即通过碱基的插入、删除和替换对RNA进行的转录后加工过程,这一表观遗传现象也被认为是在RNA水平上对遗传信息进行修复的一种修正机制。本文主要综述了目前植物中基于PPR基因家族等编辑复合体以及动物中关于CRISPR/Cas系统的两种RNA编辑系统,并介绍了RNA编辑在植物生长发育过程中的重要作用,并展望了RNA编辑研究的未来应用前景。此外,本文总结了关于RNA编辑数据库的最近研究进展,为后续的RNA编辑研究提供一定的理论参考。
朱琳, 鲜凤君, 张倩楠, 胡骏. RNA编辑的研究进展[J]. 生物技术通报, 2022, 38(1): 1-14.
ZHU Lin, XIAN Feng-jun, ZHANG Qian-nan, HU Jun. Research Progress of RNA Editing[J]. Biotechnology Bulletin, 2022, 38(1): 1-14.
序号 No. | 蛋白 Protein | 靶标基因 Target genes | 研究对象 Object | 定位 Location | 类别 Class | 氨基酸变化 Changes of amino acid | 基因表达受阻后表型 Phenotype after blocked gene expression | 文献 Reference |
---|---|---|---|---|---|---|---|---|
1 | PPS1 | nad3-155,nad3-172,nad3-173, nad3-190,nad3-191 | Rice | Mitochondria | DYW | Pro-Leu | 生长缓慢、矮化和发育迟缓、花药短小、花粉不育、柱头发芽率和结实率低 电子传递链复合体丰度及活性降低,线粒体嵴坍塌,导致其形态结构异常 | [ |
2 | PPR756 | atp6-368.ccmC-236.nad7-83 | Rice | Mitochondria | E | Pro-Leu,Pro-Leu,Ser-Leu | 营养生长时期发育迟缓,生殖生长时期花粉干瘪,产生雄性不育现象 | [ |
3 | OGR1 | cox2-167.cox3-572.ccmC-458 nad2-1457.nad4-401 nad4-416 nad4-433 | Rice | Mitochondria | DYW | Ser-Leu.Ser-Phe.Ser-Leu. Ser-Leu.Ser-Phe.Pro-Leu Leu-Phe | 生长迟缓、分蘖少、种子萌发延迟、胚乳不透明、矮化、部分不育 | [ |
4 | PGL1 | ndhD-878.ccmFc-543 | Rice | Chloroplast/Mitochondria | DYW | Ser-Leu.Val-Val | 叶色淡绿,叶绿素含量显著降低,类囊体结构排列松散 | [ |
5 | PPR16 | rpoB-545 | Rice | Chloroplast | DYW | Ser-Leu | 早期叶片黄化,后期返绿,叶绿素合成变慢 | [ |
6 | ATP4 | rps8-182 | Rice/Maize | Chloroplast | P | Ser-Leu | 低温白化,生长发育缺陷,雄性不育 | [ |
7 | SMK1 | nad7-836 | Rice/Maize | Mitochondria | E | Pro-Leu | 种子的胚和胚乳发育异常,苗期致死 | [ |
8 | EMP5 | rpl16-458 | Maize | Mitochondria | DYW | Pro-Leu | 生长迟缓,种子发育不良 | [ |
9 | Emp7 | ccmFN-1553 | Maize | Mitochondria | E | Ser-Phe | 胚和胚乳的发育受阻,胚胎致死 | [ |
10 | Emp9 | ccmB-43.rps4-335 | Maize | Mitochondria | E+ | Pro-Ser.Pro-Leu | 果皮塌陷,胚和胚乳发育受阻,胚胎致死 | [ |
11 | PPR2263 | nad5-1550.cob-908 | Maize | Mitochondria | DYW | Thr-Ile.Pro-Leu | 籽粒和幼苗生长缺陷,叶片窄短,开花晚,线粒体结构受损 | [ |
12 | AEF1/ MPR25 | atpF-92.nad5-1580 | Arabidopsis/Rice | Plastid/Mitochondria | E | Pro-Leu.Ser-Leu | 苗期生长缓慢,光合作用速率降低,叶色黄绿 | [ |
13 | SLO1 | nad4-449.nad9-328 | Arabidopsis | Mitochondria | E | Pro-Leu.Arg-Trp | 生长缓慢,发育延迟 | [ |
14 | SLO2 | nad4L-110,nad1-2,nad1-40, nad7-739,mttB-144,mttB-145,mttB-666 | Arabidopsis | Mitochondria | E+ | Ser-Leu,Thr-Met,Leu-Leu,Leu-Phe,Phe-Phe,Pro-Ser,Ser-Leu | 叶片出芽迟缓,根生长受限,开花晚 电子传递链复合体I、III和IV丰度和活性降低,碳能量失衡 | [ |
15 | MEF9 | nad7-200 | Arabidopsis | Mitochondria | E | Ser-Phe | 生长稍慢,抽薹和花座延迟 | [ |
16 | MEF10 | nad2-842 | Arabidopsis | Mitochondria | DYW | Ser-Phe | 生长延迟,没有明显的表型差异 | [ |
17 | LOI1 (MEF11) | cox3-422,ccb203-344,nad4-124 | Arabidopsis | Mitochondria | DYW | Pro-Leu,Pro-Leu,Leu-Leu | 对类异戊二烯合成的特异性抑制剂具有抗性,影响异戊二烯生物合成 | [ |
18 | MEF13 | nad7-213,ccmFc-50,ccmFc-415,cox3-314,nad2-59,nad4-158,nad5-1665,nad5-1916 | Arabidopsis | Mitochondria | E | Asp-Asp,Pro-Leu,Leu-Phe,Ser-Phe,Ser-Phe,Pro-Leu,Leu-Leu,Ser-Phe | 生长发育缓慢,莲座叶叶茎缩短 | [ |
19 | SLG1 | nad3-250 | Arabidopsis | Mitochondria | E+ | Pro-Ser | 生长缓慢和发育迟缓,对ABA的响应增强,H2O2积累增加,耐旱性增强 | [ |
20 | AHG11 | nad4-376 | Arabidopsis | Mitochondria | E+ | Cys-Arg | 影响ABA信号传递及细胞响应 | [ |
21 | OTP87 | nad7-24,atp1-1178 | Arabidopsis | Mitochondria | E | Ile- Ile,Ser-Leu | 生长缓慢,发育迟缓,株型较小 | [ |
22 | RARE1 | accD-794 | Arabidopsis | Chloroplast | DYW | Ser-Leu | 纯合突变体生长旺盛,发育迅速 | [ |
23 | CLB19 | rpoA-200,clpP-559 | Arabidopsis | Chloroplast | E+ | Ser-Phe,His-Tyr | 叶色淡黄,叶绿体发育受损,发育迟缓,幼苗早死 | [ |
24 | VAC1 | accD-794,ndhF-290 | Arabidopsis | Chloroplast | DYW | Ser-Leu | 纯合突变体白化致死,杂合突变体叶色呈浅黄绿,叶绿体发育受损 | [ |
25 | QED1 | accD-794,matK-640,ndhB-872,rpoB-2432 | Arabidopsis | Chloroplast | DYW | Ser-Leu,His-Tyr,Ser-Leu,Ser-Leu | 生长缓慢,生长5周后叶片出现黄色区域 | [ |
26 | YS1 | rpoB-338 | Arabidopsis | Chloroplast | DYW | Ser-Phe | 光合能力下降,光合色素复合物减少,叶绿体结构异常 | [ |
27 | LPA66 | psbF-77 | Arabidopsis | Chloroplast | DYW | Ser-Phe | 生长缓慢,叶色淡绿,光系统Ⅱ功能受损 | [ |
28 | AtECB2 | accD-794 | Arabidopsis | Chloroplast | DYW | Leu-Ser | 白化致死,叶绿体缺乏有组织的类囊体膜,光合蛋白水平下降 | [ |
29 | PpPPR45 | rps14-2 | Physcomitrella patens | Chloroplast | DYW | Met-Thr | 生长迟缓,颜色淡绿,光合活性降低 | [ |
30 | PpPPR56 | nad3-230,nad4-272 | Physcomitrella patens | Mitochondria | DYW | Ser-Leu | 生长发育轻微阻滞 | [ |
31 | PpPPR65 | ccmFc-103,ccmFc-122 | Physcomitrella patens | Mitochondria | DYW | Pro-Ser,Ser-Phe | 生长发育严重阻滞 | [ |
32 | PpPPR71 | ccmFc-122 | Physcomitrella patens | Mitochondria | DYW | Ser-Phe | 生长发育明显阻滞 | [ |
33 | PpPPR77 | cox2-370,cox3-733 | Physcomitrella patens | Mitochondria | DYW | Arg-Trp | 生长发育严重阻滞 | [ |
34 | PpPPR78 | cox1-755,rps14-137 | Physcomitrella patens | Mitochondria | DYW | Ser-Leu | 生长发育轻微阻滞 | [ |
35 | PpPPR79 | nad5-598 | Physcomitrella patens | Mitochondria | DYW | Arg-Cys | 生长发育严重阻滞 | [ |
36 | PpPPR91 | nad5-244 | Physcomitrella patens | Mitochondria | DYW | Arg-Trp | 生长发育严重阻滞 | [ |
37 | PpPPR98 | atp9-92 | Physcomitrella patens | Mitochondria | DYW | Ser-Leu | 生长发育无明显差异,转录水平较野生型低35% | [ |
表1 参与RNA编辑的PPR蛋白及其对模式植物生长发育的调控
Table 1 PPR protein involved in RNA editing and its regulation on model plant growth and development
序号 No. | 蛋白 Protein | 靶标基因 Target genes | 研究对象 Object | 定位 Location | 类别 Class | 氨基酸变化 Changes of amino acid | 基因表达受阻后表型 Phenotype after blocked gene expression | 文献 Reference |
---|---|---|---|---|---|---|---|---|
1 | PPS1 | nad3-155,nad3-172,nad3-173, nad3-190,nad3-191 | Rice | Mitochondria | DYW | Pro-Leu | 生长缓慢、矮化和发育迟缓、花药短小、花粉不育、柱头发芽率和结实率低 电子传递链复合体丰度及活性降低,线粒体嵴坍塌,导致其形态结构异常 | [ |
2 | PPR756 | atp6-368.ccmC-236.nad7-83 | Rice | Mitochondria | E | Pro-Leu,Pro-Leu,Ser-Leu | 营养生长时期发育迟缓,生殖生长时期花粉干瘪,产生雄性不育现象 | [ |
3 | OGR1 | cox2-167.cox3-572.ccmC-458 nad2-1457.nad4-401 nad4-416 nad4-433 | Rice | Mitochondria | DYW | Ser-Leu.Ser-Phe.Ser-Leu. Ser-Leu.Ser-Phe.Pro-Leu Leu-Phe | 生长迟缓、分蘖少、种子萌发延迟、胚乳不透明、矮化、部分不育 | [ |
4 | PGL1 | ndhD-878.ccmFc-543 | Rice | Chloroplast/Mitochondria | DYW | Ser-Leu.Val-Val | 叶色淡绿,叶绿素含量显著降低,类囊体结构排列松散 | [ |
5 | PPR16 | rpoB-545 | Rice | Chloroplast | DYW | Ser-Leu | 早期叶片黄化,后期返绿,叶绿素合成变慢 | [ |
6 | ATP4 | rps8-182 | Rice/Maize | Chloroplast | P | Ser-Leu | 低温白化,生长发育缺陷,雄性不育 | [ |
7 | SMK1 | nad7-836 | Rice/Maize | Mitochondria | E | Pro-Leu | 种子的胚和胚乳发育异常,苗期致死 | [ |
8 | EMP5 | rpl16-458 | Maize | Mitochondria | DYW | Pro-Leu | 生长迟缓,种子发育不良 | [ |
9 | Emp7 | ccmFN-1553 | Maize | Mitochondria | E | Ser-Phe | 胚和胚乳的发育受阻,胚胎致死 | [ |
10 | Emp9 | ccmB-43.rps4-335 | Maize | Mitochondria | E+ | Pro-Ser.Pro-Leu | 果皮塌陷,胚和胚乳发育受阻,胚胎致死 | [ |
11 | PPR2263 | nad5-1550.cob-908 | Maize | Mitochondria | DYW | Thr-Ile.Pro-Leu | 籽粒和幼苗生长缺陷,叶片窄短,开花晚,线粒体结构受损 | [ |
12 | AEF1/ MPR25 | atpF-92.nad5-1580 | Arabidopsis/Rice | Plastid/Mitochondria | E | Pro-Leu.Ser-Leu | 苗期生长缓慢,光合作用速率降低,叶色黄绿 | [ |
13 | SLO1 | nad4-449.nad9-328 | Arabidopsis | Mitochondria | E | Pro-Leu.Arg-Trp | 生长缓慢,发育延迟 | [ |
14 | SLO2 | nad4L-110,nad1-2,nad1-40, nad7-739,mttB-144,mttB-145,mttB-666 | Arabidopsis | Mitochondria | E+ | Ser-Leu,Thr-Met,Leu-Leu,Leu-Phe,Phe-Phe,Pro-Ser,Ser-Leu | 叶片出芽迟缓,根生长受限,开花晚 电子传递链复合体I、III和IV丰度和活性降低,碳能量失衡 | [ |
15 | MEF9 | nad7-200 | Arabidopsis | Mitochondria | E | Ser-Phe | 生长稍慢,抽薹和花座延迟 | [ |
16 | MEF10 | nad2-842 | Arabidopsis | Mitochondria | DYW | Ser-Phe | 生长延迟,没有明显的表型差异 | [ |
17 | LOI1 (MEF11) | cox3-422,ccb203-344,nad4-124 | Arabidopsis | Mitochondria | DYW | Pro-Leu,Pro-Leu,Leu-Leu | 对类异戊二烯合成的特异性抑制剂具有抗性,影响异戊二烯生物合成 | [ |
18 | MEF13 | nad7-213,ccmFc-50,ccmFc-415,cox3-314,nad2-59,nad4-158,nad5-1665,nad5-1916 | Arabidopsis | Mitochondria | E | Asp-Asp,Pro-Leu,Leu-Phe,Ser-Phe,Ser-Phe,Pro-Leu,Leu-Leu,Ser-Phe | 生长发育缓慢,莲座叶叶茎缩短 | [ |
19 | SLG1 | nad3-250 | Arabidopsis | Mitochondria | E+ | Pro-Ser | 生长缓慢和发育迟缓,对ABA的响应增强,H2O2积累增加,耐旱性增强 | [ |
20 | AHG11 | nad4-376 | Arabidopsis | Mitochondria | E+ | Cys-Arg | 影响ABA信号传递及细胞响应 | [ |
21 | OTP87 | nad7-24,atp1-1178 | Arabidopsis | Mitochondria | E | Ile- Ile,Ser-Leu | 生长缓慢,发育迟缓,株型较小 | [ |
22 | RARE1 | accD-794 | Arabidopsis | Chloroplast | DYW | Ser-Leu | 纯合突变体生长旺盛,发育迅速 | [ |
23 | CLB19 | rpoA-200,clpP-559 | Arabidopsis | Chloroplast | E+ | Ser-Phe,His-Tyr | 叶色淡黄,叶绿体发育受损,发育迟缓,幼苗早死 | [ |
24 | VAC1 | accD-794,ndhF-290 | Arabidopsis | Chloroplast | DYW | Ser-Leu | 纯合突变体白化致死,杂合突变体叶色呈浅黄绿,叶绿体发育受损 | [ |
25 | QED1 | accD-794,matK-640,ndhB-872,rpoB-2432 | Arabidopsis | Chloroplast | DYW | Ser-Leu,His-Tyr,Ser-Leu,Ser-Leu | 生长缓慢,生长5周后叶片出现黄色区域 | [ |
26 | YS1 | rpoB-338 | Arabidopsis | Chloroplast | DYW | Ser-Phe | 光合能力下降,光合色素复合物减少,叶绿体结构异常 | [ |
27 | LPA66 | psbF-77 | Arabidopsis | Chloroplast | DYW | Ser-Phe | 生长缓慢,叶色淡绿,光系统Ⅱ功能受损 | [ |
28 | AtECB2 | accD-794 | Arabidopsis | Chloroplast | DYW | Leu-Ser | 白化致死,叶绿体缺乏有组织的类囊体膜,光合蛋白水平下降 | [ |
29 | PpPPR45 | rps14-2 | Physcomitrella patens | Chloroplast | DYW | Met-Thr | 生长迟缓,颜色淡绿,光合活性降低 | [ |
30 | PpPPR56 | nad3-230,nad4-272 | Physcomitrella patens | Mitochondria | DYW | Ser-Leu | 生长发育轻微阻滞 | [ |
31 | PpPPR65 | ccmFc-103,ccmFc-122 | Physcomitrella patens | Mitochondria | DYW | Pro-Ser,Ser-Phe | 生长发育严重阻滞 | [ |
32 | PpPPR71 | ccmFc-122 | Physcomitrella patens | Mitochondria | DYW | Ser-Phe | 生长发育明显阻滞 | [ |
33 | PpPPR77 | cox2-370,cox3-733 | Physcomitrella patens | Mitochondria | DYW | Arg-Trp | 生长发育严重阻滞 | [ |
34 | PpPPR78 | cox1-755,rps14-137 | Physcomitrella patens | Mitochondria | DYW | Ser-Leu | 生长发育轻微阻滞 | [ |
35 | PpPPR79 | nad5-598 | Physcomitrella patens | Mitochondria | DYW | Arg-Cys | 生长发育严重阻滞 | [ |
36 | PpPPR91 | nad5-244 | Physcomitrella patens | Mitochondria | DYW | Arg-Trp | 生长发育严重阻滞 | [ |
37 | PpPPR98 | atp9-92 | Physcomitrella patens | Mitochondria | DYW | Ser-Leu | 生长发育无明显差异,转录水平较野生型低35% | [ |
数据库名称 Database | 整合范围 Research scope | 记录事件 Record contents | 文献 Reference |
---|---|---|---|
REDIportal | 人类 | 450多万个A-to-I类型的编辑事件 | [116] |
RADAR | 人类、小鼠、苍蝇 | 人类中1 379 403个、小鼠中8 108个和苍蝇中2 698个A-to-I类型的编辑事件 | [ |
PREPACT 3.0 | RNA编辑因子 | 编辑位点识别特异性特征编辑因子信息 | [ |
dbRES | 植物、后生动物、原生动物、真菌和病毒等96种生物 | 251个转录本中5 437个RNA编辑位点 | [ |
RESOPS | 陆地植物细胞器 | 5 754个RNA编辑位点与蛋白质三维结构的对应关系 | [ |
CloroplastDB | 植物叶绿体基因组 | 叶绿体相关RNA编辑事件 | [ |
GOBASE | 植物细胞器基因组 | 线粒体及叶绿体内RNA编辑事件类型及位点碱基的变化 | [ |
REDIdb 3.0 | 植物细胞器基因组 | 281个生物体和85个完整的细胞器基因组中的26 618个事件 | [ |
PED | 植物RNA编辑因子 | 1 621种植物和1 673个植物细胞器的203种细胞器基因上20 836个RNA编辑事件 | [ |
表2 部分RNA编辑数据库
Table 2 Partial RNA editing database
数据库名称 Database | 整合范围 Research scope | 记录事件 Record contents | 文献 Reference |
---|---|---|---|
REDIportal | 人类 | 450多万个A-to-I类型的编辑事件 | [116] |
RADAR | 人类、小鼠、苍蝇 | 人类中1 379 403个、小鼠中8 108个和苍蝇中2 698个A-to-I类型的编辑事件 | [ |
PREPACT 3.0 | RNA编辑因子 | 编辑位点识别特异性特征编辑因子信息 | [ |
dbRES | 植物、后生动物、原生动物、真菌和病毒等96种生物 | 251个转录本中5 437个RNA编辑位点 | [ |
RESOPS | 陆地植物细胞器 | 5 754个RNA编辑位点与蛋白质三维结构的对应关系 | [ |
CloroplastDB | 植物叶绿体基因组 | 叶绿体相关RNA编辑事件 | [ |
GOBASE | 植物细胞器基因组 | 线粒体及叶绿体内RNA编辑事件类型及位点碱基的变化 | [ |
REDIdb 3.0 | 植物细胞器基因组 | 281个生物体和85个完整的细胞器基因组中的26 618个事件 | [ |
PED | 植物RNA编辑因子 | 1 621种植物和1 673个植物细胞器的203种细胞器基因上20 836个RNA编辑事件 | [ |
[1] |
Sun T, Bentolila S, Hanson MR. The unexpected diversity of plant organelle RNA editosomes[J]. Trends Plant Sci, 2016, 21(11):962-973.
doi: 10.1016/j.tplants.2016.07.005 URL |
[2] |
Benne R, Van den Burg J, Brakenhoff JP, et al. Major transcript of the frameshifted coxII gene from trypanosome mitochondria contains four nucleotides that are not encoded in the DNA[J]. Cell, 1986, 46(6):819-826.
doi: 10.1016/0092-8674(86)90063-2 pmid: 3019552 |
[3] |
Hiesel R, Wissinger B, Schuster W, et al. RNA editing in plant mitochondria[J]. Science, 1989, 246(4937):1632-1634.
pmid: 2480644 |
[4] |
Hoch B, Maier RM, Appel K, et al. Editing of a chloroplast mRNA by creation of an initiation Codon[J]. Nature, 1991, 353(6340):178-180.
doi: 10.1038/353178a0 URL |
[5] |
Melcher T, Maas S, Herb A, et al. A mammalian RNA editing enzyme[J]. Nature, 1996, 379(6564):460-464.
doi: 10.1038/379460a0 URL |
[6] |
Mehta A, Driscoll DM. Identification of domains in apobec-1 complementation factor required for RNA binding and apolipoprotein-B mRNA editing[J]. RNA, 2002, 8(1):69-82.
doi: 10.1017/S1355838202015649 URL |
[7] |
Thomas SM, Lamb RA, Paterson RG. Two mRNAs that differ by two nontemplated nucleotides encode the amino coterminal proteins P and V of the paramyxovirus SV5[J]. Cell, 1988, 54(6):891-902.
pmid: 3044614 |
[8] |
Yan J, Zhang Q, Yin P. RNA editing machinery in plant organelles[J]. Sci China Life Sci, 2018, 61(2):162-169.
doi: 10.1007/s11427-017-9170-3 URL |
[9] |
Stern DB, Goldschmidt-Clermont M, Hanson MR. Chloroplast RNA metabolism[J]. Annu Rev Plant Biol, 2010, 61:125-155.
doi: 10.1146/arplant.2010.61.issue-1 URL |
[10] |
Castandet B, Choury D, Bégu D, et al. Intron RNA editing is essential for splicing in plant mitochondria[J]. Nucleic Acids Res, 2010, 38(20):7112-7121.
doi: 10.1093/nar/gkq591 pmid: 20615898 |
[11] |
Ruchika, Tsukahara T. The U-to-C RNA editing affects the mRNA stability of nuclear genes in Arabidopsis thaliana[J]. Biochem Biophys Res Commun, 2021, 571:110-117.
doi: 10.1016/j.bbrc.2021.06.098 URL |
[12] |
Chateigner-Boutin AL, Small I. Plant RNA editing[J]. RNA Biol, 2010, 7(2):213-219.
pmid: 20473038 |
[13] |
Bentolila S, Oh J, Hanson MR, et al. Comprehensive high-resolution analysis of the role of an Arabidopsis gene family in RNA editing[J]. PLoS Genet, 2013, 9(6):e1003584.
doi: 10.1371/journal.pgen.1003584 URL |
[14] |
Planchard N, Bertin P, Quadrado M, et al. The translational landscape of Arabidopsis mitochondria[J]. Nucleic Acids Res, 2018, 46(12):6218-6228.
doi: 10.1093/nar/gky489 pmid: 29873797 |
[15] |
Rugen N, Straube H, Franken LE, et al. Correction:complexome profiling reveals association of PPR proteins with ribosomes in the mitochondria of plants[J]. Mol Cell Proteom, 2019, 18(8):1704.
doi: 10.1074/mcp.AAC119.001674 URL |
[16] |
Ran FA, Hsu PD, Wright J, et al. Genome engineering using the CRISPR-Cas9 system[J]. Nat Protoc, 2013, 8(11):2281-2308.
doi: 10.1038/nprot.2013.143 URL |
[17] | Konermann S, Lotfy P, Brideau NJ, et al. Transcriptome engineering with RNA-targeting type VI-D CRISPR effectors[J]. Cell, 2018, 173(3):665-676. e14. |
[18] |
Özcan A, Krajeski R, Ioannidi E, et al. Programmable RNA targeting with the single-protein CRISPR effector Cas7-11[J]. Nature, 2021, 597(7878):720-725.
doi: 10.1038/s41586-021-03886-5 URL |
[19] | Smargon AA, Cox DBT, Pyzocha NK, et al. Cas13b is a type VI-B CRISPR-associated RNA-guided RNase differentially regulated by accessory proteins Csx27 and Csx28[J]. Mol Cell, 2017, 65(4):618-630. e7. |
[20] |
Small ID, Rackham O, Filipovska A. Organelle transcriptomes:products of a deconstructed genome[J]. Curr Opin Microbiol, 2013, 16(5):652-658.
doi: 10.1016/j.mib.2013.07.011 pmid: 23932204 |
[21] |
Jacobs J, Kück U. Function of chloroplast RNA-binding proteins[J]. Cell Mol Life Sci, 2011, 68(5):735-748.
doi: 10.1007/s00018-010-0523-3 URL |
[22] |
Small ID, Peeters N. The PPR motif - a TPR-related motif prevalent in plant organellar proteins[J]. Trends Biochem Sci, 2000, 25(2):46-47.
pmid: 10664580 |
[23] |
Nakamura T, Yagi Y, Kobayashi K. Mechanistic insight into pentatricopeptide repeat proteins as sequence-specific RNA-binding proteins for organellar RNAs in plants[J]. Plant Cell Physiol, 2012, 53(7):1171-1179.
doi: 10.1093/pcp/pcs069 URL |
[24] |
Lurin C, Andrés C, Aubourg S, et al. Genome-wide analysis of Arabidopsis pentatricopeptide repeat proteins reveals their essential role in organelle biogenesis[J]. Plant Cell, 2004, 16(8):2089-2103.
doi: 10.1105/tpc.104.022236 URL |
[25] |
Schmitz-Linneweber C, Small I. Pentatricopeptide repeat proteins:a socket set for organelle gene expression[J]. Trends Plant Sci, 2008, 13(12):663-670.
doi: 10.1016/j.tplants.2008.10.001 pmid: 19004664 |
[26] | Shikanai T. RNA editing in plants:Machinery and flexibility of site recognition[J]. Biochim et Biophys Acta BBA Bioenerg, 2015, 1847(9):779-785. |
[27] |
Barkan A, Small I. Pentatricopeptide repeat proteins in plants[J]. Annu Rev Plant Biol, 2014, 65:415-442.
doi: 10.1146/annurev-arplant-050213-040159 pmid: 24471833 |
[28] |
Leu KC, Hsieh MH, Wang HJ, et al. Distinct role of Arabidopsis mitochondrial P-type pentatricopeptide repeat protein-modulating editing protein, PPME, in nad1 RNA editing[J]. RNA Biol, 2016, 13(6):593-604.
doi: 10.1080/15476286.2016.1184384 URL |
[29] |
Okuda K, Myouga F, Motohashi R, et al. Conserved domain structure of pentatricopeptide repeat proteins involved in chloroplast RNA editing[J]. PNAS, 2007, 104(19):8178-8183.
doi: 10.1073/pnas.0700865104 URL |
[30] |
Shikanai T. RNA editing in plant organelles:machinery, physiological function and evolution[J]. Cell Mol Life Sci, 2006, 63(6):698-708.
pmid: 16465445 |
[31] |
Aubourg S, Boudet N, Kreis M, et al. In Arabidopsis thaliana, 1% of the genome codes for a novel protein family unique to plants[J]. Plant Mol Biol, 2000, 42(4):603-613.
pmid: 10809006 |
[32] |
Betts L, Xiang SB, Short SA, et al. Cytidine deaminase. the 2·3 Å crystal structure of an enzyme:transition-state analog complex[J]. J Mol Biol, 1994, 235(2):635-656.
pmid: 8289286 |
[33] |
Salone V, Rüdinger M, Polsakiewicz M, et al. A hypojournal on the identification of the editing enzyme in plant organelles[J]. FEBS Lett, 2007, 581(22):4132-4138.
doi: 10.1016/j.febslet.2007.07.075 URL |
[34] |
Hayes ML, Giang K, Berhane B, et al. Identification of two pentatricopeptide repeat genes required for RNA editing and zinc binding by C-terminal cytidine deaminase-like domains[J]. J Biol Chem, 2013, 288(51):36519-36529.
doi: 10.1074/jbc.M113.485755 URL |
[35] |
Hayes ML, Santibanez PI. A plant pentatricopeptide repeat protein with a DYW-deaminase domain is sufficient for catalyzing C-to-U RNA editing in vitro[J]. J Biol Chem, 2020, 295(11):3497-3505.
doi: 10.1074/jbc.RA119.011790 URL |
[36] |
Oldenkott B, Yang Y, Lesch E, et al. Plant-type pentatricopeptide repeat proteins with a DYW domain drive C-to-U RNA editing in Escherichia coli[J]. Commun Biol, 2019, 2:85.
doi: 10.1038/s42003-019-0328-3 pmid: 30854477 |
[37] | Hayes ML, Hanson MR. Assay of editing of exogenous RNAs in chloroplast extracts of Arabidopsis, maize, pea, and tobacco[J]. Methods Enzymol, 2007, 424:459-482. |
[38] |
Okuda K, Nakamura T, Sugita M, et al. A pentatricopeptide repeat protein is a site recognition factor in chloroplast RNA editing[J]. J Biol Chem, 2006, 281(49):37661-37667.
doi: 10.1074/jbc.M608184200 URL |
[39] |
Barkan A, Rojas M, Fujii S, et al. A combinatorial amino acid code for RNA recognition by pentatricopeptide repeat proteins[J]. PLoS Genet, 2012, 8(8):e1002910.
doi: 10.1371/journal.pgen.1002910 URL |
[40] |
Yagi Y, Hayashi S, Kobayashi K, et al. Elucidation of the RNA recognition code for pentatricopeptide repeat proteins involved in organelle RNA editing in plants[J]. PLoS One, 2013, 8(3):e57286.
doi: 10.1371/journal.pone.0057286 URL |
[41] |
Yin P, Li Q, Yan C, et al. Structural basis for the modular recognition of single-stranded RNA by PPR proteins[J]. Nature, 2013, 504(7478):168-171.
doi: 10.1038/nature12651 URL |
[42] |
Xiao HJ, Zhang QN, Qin XJ, et al. Rice PPS1 encodes a DYW motif-containing pentatricopeptide repeat protein required for five consecutive RNA-editing sites of nad3 in mitochondria[J]. New Phytol, 2018, 220(3):878-892.
doi: 10.1111/nph.15347 URL |
[43] |
Zhang Q, Xu Y, Huang J, et al. The rice pentatricopeptide repeat protein PPR756 is involved in pollen development by affecting multiple RNA editing in mitochondria[J]. Front Plant Sci, 2020, 11:749.
doi: 10.3389/fpls.2020.00749 URL |
[44] |
Kim SR, Yang JI, Moon S, et al. Rice OGR1 encodes a pentatricopeptide repeat-DYW protein and is essential for RNA editing in mitochondria[J]. Plant J, 2009, 59(5):738-749.
doi: 10.1111/tpj.2009.59.issue-5 URL |
[45] | Xiao H, Xu Y, Ni C, et al. A rice dual-localized pentatricopeptide repeat protein is involved in organellar RNA editing together with OsMORFs[J]. J Exp Bot, 2018, 69(12):2923-2936. |
[46] |
Huang W, Zhang Y, Shen L, et al. Accumulation of the RNA polymerase subunit RpoB depends on RNA editing by OsPPR16 and affects chloroplast development during early leaf development in rice[J]. New Phytol, 2020, 228(4):1401-1416.
doi: 10.1111/nph.v228.4 URL |
[47] |
Zhang J, Guo Y, Fang Q, et al. The PPR-SMR protein ATP4 is required for editing the chloroplast rps8 mRNA in rice and maize[J]. Plant Physiol, 2020, 184(4):2011-2021.
doi: 10.1104/pp.20.00849 URL |
[48] |
Li XJ, Zhang YF, Hou M, et al. Small kernel 1 encodes a pentatricopeptide repeat protein required for mitochondrial nad7 transcript editing and seed development in maize(Zea mays)and rice(Oryza sativa)[J]. Plant J, 2014, 79(5):797-809.
doi: 10.1111/tpj.2014.79.issue-5 URL |
[49] |
Zheng P, He Q, Wang XM, et al. Functional analysis for domains of maize PPR protein EMP5 in RNA editing and plant development in Arabidopsis[J]. Plant Growth Regul, 2019, 87(1):19-27.
doi: 10.1007/s10725-018-0447-8 |
[50] |
Sun F, Wang XM, Bonnard G, et al. Empty pericarp7encodes a mitochondrial E-subgroup pentatricopeptide repeat protein that is required forccmFNediting, mitochondrial function and seed development in maize[J]. Plant J, 2015, 84(2):283-295.
doi: 10.1111/tpj.12993 URL |
[51] |
Yang YZ, Ding S, Wang HC, et al. The pentatricopeptide repeat protein EMP9 is required for mitochondrial ccmB and rps4 transcript editing, mitochondrial complex biogenesis and seed development in maize[J]. New Phytol, 2017, 214(2):782-795.
doi: 10.1111/nph.14424 pmid: 28121385 |
[52] |
Sosso D, Mbelo S, Vernoud V, et al. PPR2263, a DYW-Subgroup Pentatricopeptide repeat protein, is required for mitochondrial nad5 and cob transcript editing, mitochondrion biogenesis, and maize growth[J]. Plant Cell, 2012, 24(2):676-691.
doi: 10.1105/tpc.111.091074 URL |
[53] |
Yap A, Kindgren P, Colas des Francs-Small C, et al. AEF1/MPR25 is implicated in RNA editing of plastid atpF and mitochondrial nad5, and also promotes atpF splicing in Arabidopsis and rice[J]. Plant J, 2015, 81(5):661-669.
doi: 10.1111/tpj.2015.81.issue-5 URL |
[54] |
Toda T, Fujii S, Noguchi K, et al. Rice MPR25 encodes a pentatricopeptide repeat protein and is essential for RNA editing of nad5 transcripts in mitochondria[J]. Plant J, 2012, 72(3):450-460.
doi: 10.1111/tpj.2012.72.issue-3 URL |
[55] |
Sung TY, Tseng CC, Hsieh MH. The SLO1 PPR protein is required for RNA editing at multiple sites with similar upstream sequences in Arabidopsis mitochondria[J]. Plant J, 2010, 63(3):499-511.
doi: 10.1111/tpj.2010.63.issue-3 URL |
[56] |
Zhu Q, Dugardeyn J, Zhang C, et al. SLO2, a mitochondrial pentatricopeptide repeat protein affecting several RNA editing sites, is required for energy metabolism[J]. Plant J, 2012, 71(5):836-849.
doi: 10.1111/tpj.2012.71.issue-5 URL |
[57] |
Takenaka M. MEF9, an E-subclass pentatricopeptide repeat protein, is required for an RNA editing event in the nad7 transcript in mitochondria of Arabidopsis[J]. Plant Physiol, 2010, 152(2):939-947.
doi: 10.1104/pp.109.151175 pmid: 20018598 |
[58] |
Härtel B, Zehrmann A, Verbitskiy D, et al. MEF10 is required for RNA editing at nad2-842 in mitochondria of Arabidopsis thaliana and interacts with MORF8[J]. Plant Mol Biol, 2013, 81(4/5):337-346.
doi: 10.1007/s11103-012-0003-2 URL |
[59] |
Tang J, Kobayashi K, Suzuki M, et al. The mitochondrial PPR protein LOVASTATIN INSENSITIVE 1 plays regulatory roles in cytosolic and plastidial isoprenoid biosynjournal through RNA editing[J]. Plant J, 2010, 61(3):456-466.
doi: 10.1111/tpj.2010.61.issue-3 URL |
[60] |
Glass F, Härtel B, Zehrmann A, et al. MEF13 requires MORF3 and MORF8 for RNA editing at eight targets in mitochondrial mRNAs in Arabidopsis thaliana[J]. Mol Plant, 2015, 8(10):1466-1477.
doi: 10.1016/j.molp.2015.05.008 URL |
[61] |
Yuan H, Liu D. Functional disruption of the pentatricopeptide protein SLG1 affects mitochondrial RNA editing, plant development, and responses to abiotic stresses in Arabidopsis[J]. Plant J, 2012, 70(3):432-444.
doi: 10.1111/tpj.2012.70.issue-3 URL |
[62] |
Greco M, Chiappetta A, Bruno L, et al. In Posidonia oceanica cadmium induces changes in DNA methylation and chromatin patterning[J]. J Exp Bot, 2012, 63(2):695-709.
doi: 10.1093/jxb/err313 URL |
[63] |
Hammani K, Francs-Small CC, Takenaka M, et al. The pentatricopeptide repeat protein OTP87 is essential for RNA editing of nad7 and atp1 transcripts in Arabidopsis mitochondria[J]. J Biol Chem, 2011, 286(24):21361-21371.
doi: 10.1074/jbc.M111.230516 pmid: 21504904 |
[64] |
Robbins JC, Heller WP, Hanson MR. A comparative genomics approach identifies a PPR-DYW protein that is essential for C-to-U editing of the Arabidopsis chloroplast accD transcript[J]. RNA, 2009, 15(6):1142-1153.
doi: 10.1261/rna.1533909 pmid: 19395655 |
[65] |
Chateigner-Boutin AL, Ramos-Vega M, Guevara-García A, et al. CLB19, a pentatricopeptide repeat protein required for editing of rpoA and clpP chloroplast transcripts[J]. Plant J, 2008, 56(4):590-602.
doi: 10.1111/tpj.2008.56.issue-4 URL |
[66] |
Tseng CC, Sung TY, Li YC, et al. Editing of accD and ndhF chloroplast transcripts is partially affected in the Arabidopsis Vanilla cream1 mutant[J]. Plant Mol Biol, 2010, 73(3):309-323.
doi: 10.1007/s11103-010-9616-5 URL |
[67] |
Wagoner JA, Sun T, Lin L, et al. Cytidine deaminase motifs within the DYW domain of two pentatricopeptide repeat-containing proteins are required for site-specific chloroplast RNA editing[J]. J Biol Chem, 2015, 290(5):2957-2968.
doi: 10.1074/jbc.M114.622084 URL |
[68] |
Zhou W, Cheng Y, Yap A, et al. The Arabidopsis gene YS1 encoding a DYW protein is required for editing of rpoB transcripts and the rapid development of chloroplasts during early growth[J]. Plant J, 2009, 58(1):82-96.
doi: 10.1111/j.1365-313X.2008.03766.x URL |
[69] |
Cai W, Ji D, Peng L, et al. LPA66 is required for editing psbF chloroplast transcripts in Arabidopsis[J]. Plant Physiol, 2009, 150(3):1260-1271.
doi: 10.1104/pp.109.136812 URL |
[70] |
Yu QB, Jiang Y, Chong K, et al. AtECB2, a pentatricopeptide repeat protein, is required for chloroplast transcript accD RNA editing and early chloroplast biogenesis in Arabidopsis thaliana[J]. Plant J, 2009, 59(6):1011-1023.
doi: 10.1111/tpj.2009.59.issue-6 URL |
[71] |
Ichinose M, Uchida M, Sugita M. Identification of a pentatricopeptide repeat RNA editing factor in Physcomitrella patens chloroplasts[J]. FEBS Lett, 2014, 588(21):4060-4064.
doi: 10.1016/j.febslet.2014.09.031 pmid: 25277299 |
[72] |
Ohtani S, Ichinose M, Tasaki E, et al. Targeted gene disruption identifies three PPR-DYW proteins involved in RNA editing for five editing sites of the moss mitochondrial transcripts[J]. Plant Cell Physiol, 2010, 51(11):1942-1949.
doi: 10.1093/pcp/pcq142 URL |
[73] |
Ichinose M, Sugita C, Yagi Y, et al. Two DYW subclass PPR proteins are involved in RNA editing of ccmFc and atp9 transcripts in the moss Physcomitrella patens:first complete set of PPR editing factors in plant mitochondria[J]. Plant Cell Physiol, 2013, 54(11):1907-1916.
doi: 10.1093/pcp/pct132 pmid: 24058147 |
[74] |
Tasaki E, Hattori M, Sugita M. The moss pentatricopeptide repeat protein with a DYW domain is responsible for RNA editing of mitochondrial ccmFc transcript[J]. Plant J, 2010, 62(4):560-570.
doi: 10.1111/tpj.2010.62.issue-4 URL |
[75] |
Uchida M, Ohtani S, Ichinose M, et al. The PPR-DYW proteins are required for RNA editing of rps14, cox1 and nad5 transcripts in Physcomitrella patens mitochondria[J]. FEBS Lett, 2011, 585(14):2367-2371.
doi: 10.1016/j.febslet.2011.06.009 URL |
[76] | Bentolila S, Heller WP, Sun T, et al. RIP1, a member of an Arabidopsis protein family, interacts with the protein RARE1 and broadly affects RNA editing[J]. Proceedings of the National Academy of Sciences of the United States of America, 2012, 109(22):E1453-1461. |
[77] |
Yang Y, Zhu G, Li R, et al. The RNA editing factor SlORRM4 is required for normal fruit ripening in tomato[J]. Plant Physiol, 2017, 175(4):1690-1702.
doi: 10.1104/pp.17.01265 URL |
[78] |
Sun T, Shi XW, Friso G, et al. A zinc finger motif-containing protein is essential for chloroplast RNA editing[J]. PLoS Genet, 2015, 11(3):e1005028.
doi: 10.1371/journal.pgen.1005028 URL |
[79] | Bayer-Császár E, Haag S, Jörg A, et al. The conserved domain in MORF proteins has distinct affinities to the PPR and E elements in PPR RNA editing factors[J]. Biochim et Biophys Acta BBA Gene Regul Mech, 2017, 1860(8):813-828. |
[80] |
Tillich M, Hardel SL, Kupsch C, et al. Chloroplast ribonucleoprotein CP31A is required for editing and stability of specific chloroplast mRNAs[J]. PNAS, 2009, 106(14):6002-6007.
doi: 10.1073/pnas.0808529106 URL |
[81] |
Zhang F, Tang W, Hedtke B, et al. Tetrapyrrole biosynthetic enzyme protoporphyrinogen IX oxidase 1 is required for plastid RNA editing[J]. PNAS, 2014, 111(5):2023-2028.
doi: 10.1073/pnas.1316183111 pmid: 24497494 |
[82] |
Coego A, Ramirez V, Gil MJ, et al. An Arabidopsis homeodomain transcription factor, OVEREXPRESSOR OF CATIONIC PEROXIDASE 3, mediates resistance to infection by necrotrophic pathogens[J]. Plant Cell, 2005, 17(7):2123-2137.
doi: 10.1105/tpc.105.032375 URL |
[83] |
Takenaka M, Brennicke A. Multiplex single-base extension typing to identify nuclear genes required for RNA editing in plant organelles[J]. Nucleic Acids Res, 2009, 37(2):e13.
doi: 10.1093/nar/gkn975 URL |
[84] |
Zhao X, Huang J, Chory J. GUN1 interacts with MORF2 to regulate plastid RNA editing during retrograde signaling[J]. PNAS, 2019, 116(20):10162-10167.
doi: 10.1073/pnas.1820426116 URL |
[85] |
Takenaka M, Zehrmann A, Verbitskiy D, et al. Multiple organellar RNA editing factor(MORF)family proteins are required for RNA editing in mitochondria and plastids of plants[J]. PNAS, 2012, 109(13):5104-5109.
doi: 10.1073/pnas.1202452109 pmid: 22411807 |
[86] |
Hackett JB, Shi X, Kobylarz AT, et al. An organelle RNA recognition motif protein is required for photosystem II subunit psbF transcript editing[J]. Plant Physiol, 2017, 173(4):2278-2293.
doi: 10.1104/pp.16.01623 pmid: 28213559 |
[87] |
Shi X, Castandet B, Germain A, et al. ORRM5, an RNA recognition motif-containing protein, has a unique effect on mitochondrial RNA editing[J]. J Exp Bot, 2017, 68(11):2833-2847.
doi: 10.1093/jxb/erx139 URL |
[88] |
Shi X, Hanson MR, Bentolila S. Two RNA recognition motif-containing proteins are plant mitochondrial editing factors[J]. Nucleic Acids Res, 2015, 43(7):3814-3825.
doi: 10.1093/nar/gkv245 URL |
[89] |
Andrés-Colás N, Zhu Q, Takenaka M, et al. Multiple PPR protein interactions are involved in the RNA editing system in Arabidopsis mitochondria and plastids[J]. PNAS, 2017, 114(33):8883-8888.
doi: 10.1073/pnas.1705815114 pmid: 28761003 |
[90] |
Guillaumot D, Lopez-Obando M, Baudry K, et al. Two interacting PPR proteins are major Arabidopsis editing factors in plastid and mitochondria[J]. PNAS, 2017, 114(33):8877-8882.
doi: 10.1073/pnas.1705780114 pmid: 28760958 |
[91] |
Kupsch C, Ruwe H, Gusewski S, et al. Arabidopsis chloroplast RNA binding proteins CP31A and CP29A associate with large transcript pools and confer cold stress tolerance by influencing multiple chloroplast RNA processing steps[J]. Plant Cell, 2012, 24(10):4266-4280.
doi: 10.1105/tpc.112.103002 URL |
[92] |
García-Andrade J, Ramírez V, López A, et al. Mediated plastid RNA editing in plant immunity[J]. PLoS Pathog, 2013, 9(10):e1003713.
doi: 10.1371/journal.ppat.1003713 URL |
[93] |
Ichinose M, Sugita M. RNA editing and its molecular mechanism in plant organelles[J]. Genes, 2016, 8(1):5.
doi: 10.3390/genes8010005 URL |
[94] |
Blanc V, Davidson NO. APOBEC-1-mediated RNA editing[J]. Wiley Interdiscip Rev Syst Biol Med, 2010, 2(5):594-602.
doi: 10.1002/wsbm.v2:5 URL |
[95] |
Qin YR, Qiao JJ, Chan TH, et al. Adenosine-to-inosine RNA editing mediated by ADARs in esophageal squamous cell carcinoma[J]. Cancer Res, 2014, 74(3):840-851.
doi: 10.1158/0008-5472.CAN-13-2545 URL |
[96] |
East-Seletsky A, O’Connell MR, Knight SC, et al. Two distinct RNase activities of CRISPR-C2c2 enable guide-RNA processing and RNA detection[J]. Nature, 2016, 538(7624):270-273.
doi: 10.1038/nature19802 URL |
[97] | Abudayyeh OO, Gootenberg JS, Konermann S, et al. C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector[J]. Science, 2016, 353(6299):aaf5573. |
[98] |
Jing X, Xie B, Chen L, et al. Implementation of the CRISPR-Cas13a system in fission yeast and its repurposing for precise RNA editing[J]. Nucleic Acids Res, 2018, 46(15):e90.
doi: 10.1093/nar/gky433 URL |
[99] |
Cox DBT, Gootenberg JS, Abudayyeh OO, et al. RNA editing with CRISPR-Cas13[J]. Science, 2017, 358(6366):1019-1027.
doi: 10.1126/science.aaq0180 URL |
[100] |
Abudayyeh OO, Gootenberg JS, Franklin B, et al. A cytosine deaminase for programmable single-base RNA editing[J]. Science, 2019, 365(6451):382-386.
doi: 10.1126/science.aax7063 pmid: 31296651 |
[101] | Liu L, Li X, Ma J, et al. The molecular architecture for RNA-guided RNA cleavage by Cas13a[J]. Cell, 2017, 170(4):714-726. e10. |
[102] |
Knott GJ, East-Seletsky A, Cofsky JC, et al. Guide-bound structures of an RNA-targeting A-cleaving CRISPR-Cas13a enzyme[J]. Nat Struct Mol Biol, 2017, 24(10):825-833.
doi: 10.1038/nsmb.3466 URL |
[103] |
Wolter F, Puchta H. The CRISPR/Cas revolution reaches the RNA world:Cas13, a new Swiss Army knife for plant biologists[J]. Plant J, 2018, 94(5):767-775.
doi: 10.1111/tpj.2018.94.issue-5 URL |
[104] | Yan WX, Chong S, Zhang H, et al. Cas13d is a compact RNA-targeting type VI CRISPR effector positively modulated by a WYL-domain-containing accessory protein[J]. Mol Cell, 2018, 70(2):339. e5. |
[105] |
Wang Q, Liu Y, Han C, et al. Efficient RNA virus targeting via CRISPR/CasRx in fish[J]. J Virol, 2021, 95(19):e0046121.
doi: 10.1128/JVI.00461-21 URL |
[106] |
Huynh N, Depner N, Larson R, et al. A versatile toolkit for CRISPR-Cas13-based RNA manipulation in Drosophila[J]. Genome Biol, 2020, 21(1):279.
doi: 10.1186/s13059-020-02193-y pmid: 33203452 |
[107] |
Brogan DJ, Chaverra-Rodriguez D, Lin CP, et al. Development of a Rapid and Sensitive CasRx-Based Diagnostic Assay for SARS-CoV-2[J]. ACS Sens, 2021, 6(11):3957-3966.
doi: 10.1021/acssensors.1c01088 URL |
[108] | Manghwar H, Li B, Ding X, et al. CRISPR/cas systems in genome editing:methodologies and tools for sgRNA design, off-target evaluation, and strategies to mitigate off-target effects[J]. Adv Sci:Weinh, 2020, 7(6):1902312. |
[109] |
Grünewald J, Zhou R, Garcia SP, et al. Transcriptome-wide off-target RNA editing induced by CRISPR-guided DNA base editors[J]. Nature, 2019, 569(7756):433-437.
doi: 10.1038/s41586-019-1161-z URL |
[110] |
Abudayyeh OO, Gootenberg JS, Essletzbichler P, et al. RNA targeting with CRISPR-Cas13[J]. Nature, 2017, 550(7675):280-284.
doi: 10.1038/nature24049 URL |
[111] | Heaton SM. Harnessing host-virus evolution in antiviral therapy and immunotherapy[J]. Clin Transl Immunology, 2019, 8(7):e1067. |
[112] |
Aman R, Ali Z, Butt H, et al. RNA virus interference via CRISPR/Cas13a system in plants[J]. Genome Biol, 2018, 19(1):1.
doi: 10.1186/s13059-017-1381-1 URL |
[113] |
Cao Y, Zhou H, Zhou X, et al. Conferring resistance to plant RNA viruses with the CRISPR/CasRx system[J]. Virol Sin, 2021, 36(4):814-817.
doi: 10.1007/s12250-020-00338-8 URL |
[114] |
Lo Giudice C, Pesole G, Picardi E. REDIdb 3. 0:a comprehensive collection of RNA editing events in plant organellar genomes[J]. Front Plant Sci, 2018, 9:482.
doi: 10.3389/fpls.2018.00482 URL |
[115] |
Li M, Xia L, Zhang Y, et al. Plant editosome database:a curated database of RNA editosome in plants[J]. Nucleic Acids Res, 2019, 47(d1):D170-D174.
doi: 10.1093/nar/gky1026 URL |
[116] |
Picardi E, D’Erchia AM, Lo Giudice C, et al. REDIportal:a comprehensive database of A-to-I RNA editing events in humans[J]. Nucleic Acids Res, 2017, 45(d1):D750-D757.
doi: 10.1093/nar/gkw767 URL |
[117] |
Ramaswami G, Li JB. RADAR:a rigorously annotated database of A-to-I RNA editing[J]. Nucleic Acids Res, 2014, 42(D1):D109-D113.
doi: 10.1093/nar/gkt996 URL |
[118] |
Lenz H, Hein A, Knoop V. Plant organelle RNA editing and its specificity factors:enhancements of analyses and new database features in PREPACT 3. 0[J]. BMC Bioinformatics, 2018, 19(1):255.
doi: 10.1186/s12859-018-2244-9 URL |
[119] |
He T, Du P, Li Y. dbRES:a web-oriented database for annotated RNA editing sites[J]. Nucleic Acids Res, 2007, 35(database issue):D141-D144.
doi: 10.1093/nar/gkl815 URL |
[120] |
Yura K, Sulaiman S, Hatta Y, et al. RESOPS:a database for analyzing the correspondence of RNA editing sites to protein three-dimensional structures[J]. Plant Cell Physiol, 2009, 50(11):1865-1873.
doi: 10.1093/pcp/pcp132 pmid: 19808808 |
[121] |
Cui L, Veeraraghavan N, Richter A, et al. ChloroplastDB:the chloroplast genome database[J]. Nucleic Acids Res, 2006, 34(database issue):D692-D696.
doi: 10.1093/nar/gkj055 URL |
[122] |
O’Brien EA, Zhang Y, Wang E, et al. GOBASE:an organelle genome database[J]. Nucleic Acids Res, 2009, 37(database issue):D946-D950.
doi: 10.1093/nar/gkn819 URL |
[1] | 刘佳慧, 刘叶, 花尔并, 王猛. 谷氨酸棒杆菌中胞嘧啶碱基编辑工具的PAM拓展[J]. 生物技术通报, 2023, 39(9): 49-57. |
[2] | 陈小玲, 廖东庆, 黄尚飞, 陈英, 芦志龙, 陈东. 利用CRISPR/Cas9系统改造酿酒酵母的研究进展[J]. 生物技术通报, 2023, 39(8): 148-158. |
[3] | 杨玉梅, 张坤晓. 应用CRISPR/Cas9技术建立ERK激酶相分离荧光探针定点整合的稳定细胞株[J]. 生物技术通报, 2023, 39(8): 159-164. |
[4] | 施炜涛, 姚春鹏, 魏文康, 王蕾, 房元杰, 仝钰洁, 马晓姣, 蒋文, 张晓爱, 邵伟. 利用CRISPR/Cas9技术构建MDH2敲除细胞株及抗呕吐毒素效应研究[J]. 生物技术通报, 2023, 39(7): 307-315. |
[5] | 刘晓燕, 祝振亮, 史广宇, 华梓宇, 杨晨, 张涌, 刘军. 乳腺生物反应器的表达优化策略[J]. 生物技术通报, 2023, 39(5): 77-91. |
[6] | 程静雯, 曹磊, 张艳敏, 叶倩, 陈敏, 谭文松, 赵亮. CHO细胞多基因工程改造策略的建立及应用[J]. 生物技术通报, 2023, 39(2): 283-291. |
[7] | 黄文莉, 李香香, 周炆婷, 罗莎, 姚维嘉, 马杰, 张芬, 沈钰森, 顾宏辉, 王建升, 孙勃. 利用CRISPR/Cas9技术靶向编辑青花菜BoZDS[J]. 生物技术通报, 2023, 39(2): 80-87. |
[8] | 王兵, 赵会纳, 余婧, 陈杰, 骆梅, 雷波. 利用CRISPR/Cas9系统研究REVOLUTA参与烟草叶芽发育的调控[J]. 生物技术通报, 2023, 39(10): 197-208. |
[9] | 李双喜, 华进联. 抗猪繁殖与呼吸障碍综合征基因编辑猪研究进展[J]. 生物技术通报, 2023, 39(10): 50-57. |
[10] | 林蓉, 郑月萍, 徐雪珍, 李丹丹, 郑志富. 拟南芥ACOL8基因在乙烯合成与响应中的功能分析[J]. 生物技术通报, 2023, 39(1): 157-165. |
[11] | 唐光甫, 桂艳玲, 满海乔, 赵杰宏. 利用CRISPR/Cas 9编辑红曲霉pyrG基因对其次生代谢的影响[J]. 生物技术通报, 2022, 38(8): 198-205. |
[12] | 赖昕彤, 王柯岚, 由雨欣, 谭俊杰. 基于CRISPR/Cas系统的DNA碱基编辑研究进展[J]. 生物技术通报, 2022, 38(6): 1-12. |
[13] | 刘静静, 刘晓蕊, 李琳, 王盈, 杨海元, 戴一凡. 利用CRISPR/Cas9技术建立OXTR基因敲除猪胎儿成纤维细胞系[J]. 生物技术通报, 2022, 38(6): 272-278. |
[14] | 陈映丹, 张扬, 夏嫱, 孙虹霞. CRISPR/Cas基因编辑技术及其在微藻研究中的应用[J]. 生物技术通报, 2022, 38(5): 257-268. |
[15] | Olalekan Amoo, 胡利民, 翟云孤, 范楚川, 周永明. 利用基因编辑技术研究BRANCHED1参与油菜分枝过程的调控[J]. 生物技术通报, 2022, 38(4): 97-105. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||