Biotechnology Bulletin ›› 2024, Vol. 40 ›› Issue (1): 127-144.doi: 10.13560/j.cnki.biotech.bull.1985.2023-0445
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YANG Shuai-peng1(), QU Zi-xiao1, ZHU Xiang-xing2, TANG Dong-sheng1,2()
Received:
2023-04-12
Online:
2024-01-26
Published:
2024-02-06
Contact:
TANG Dong-sheng
E-mail:806420672@qq.com;tangdsh@163.com
YANG Shuai-peng, QU Zi-xiao, ZHU Xiang-xing, TANG Dong-sheng. Optimization of DNA Base Editing Technology and Its Application in Pig Genetic Modification[J]. Biotechnology Bulletin, 2024, 40(1): 127-144.
Fig. 1 Mechanisms of base editor systems A: Having BE3 as an example, the base editor consists of important components nCas9, rAPOBEC1, and UGI. sgRNA and nCas9 identify specific DNA targets, then in the editable window, the rAPOBEC1 deaminates C to U, UGI inhibits U from changing to AP state, and finally changes C G to T A through DNA replication and repair mechanism. B: Having ABE7.10 as an example, the base editor consists of important components nCas9 and TadA-TadA*. sgRNA and nCas9 identify specific DNA targets, then in the editable window, the TadA-TadA* deaminates A to I, and finally changes A T into G C through DNA replication and repair mechanism. C: Having CGBE1 as an example, important components of the base editor include nCas9, then in the editable window, rAPOBEC1 deaminates C to U, and UNG. sgRNA and nCas9 identify specific DNA targets, rAPOBEC1 is responsible for deamination of C in the editable window to U, UNG promotes the formation of AP status at the U site, and finally changes C into A/G through DNA replication and repair mechanism. D: AYBE adds MPG on the basis of ABE. A becomes AP state after deamination and MPG effect, and finally becomes C/T through DNA replication and repair mechanism. After DNA replication and repair mechanism, A will finally become C/T. The AP state will form Indels
名称 Name | Cas蛋白 Cas protein | 工具酶 Tool enzyme | PAM序列 PAM sequence | NLS | 附加原件 Additional original | 密码子优化 Codon optimiz-ation | 编辑窗口 Editing window |
---|---|---|---|---|---|---|---|
BE1[ | dCas9 | rAPOBEC1 | NGG | 1× | - | - | 4-8 |
BE2[ | dCas9 | rAPOBEC1 | NGG | 1× | 1×UGI | - | 4-8 |
BE3[ | nCas9 | rAPOBEC1 | NGG | 1× | 1×UGI | - | 4-8 |
BE3-R33A[ | nCas9 | rAPOBEC1R33A | NGG | 1× | 1×UGI | - | 5-7 |
BE3-R33A/K34A[ | nCas9 | rAPOBEC1R33A/K34A | NGG | 1× | 1×UGI | - | 5-6 |
Target-AID[ | nCas9 | PmCDA1 | NGG | 1× | 1×UGI | - | 2-8 |
TAM[ | dCas9 | hAIDx | NGG | 1× | 1×UGI | - | 4-10 |
CRISPR-X[ | dCas9 | hAIDΔ-MS2 | NGG | 1× | - | - | -50-50 |
ZF-hAID[ | ZF | hAID | less | 1× | 1×UGI | - | - |
TALE-hAID[ | TALE | hAID | less | 1× | 1×UGI | - | - |
BE4[ | nCas9 | rAPOBEC1 | NGG | 1× | 2×UGI | - | 4-8 |
BE4Gam[ | nCas9 | rAPOBEC1 | NGG | 1× | 2×UGI 1×Gam | - | 4-8 |
eBE[ | nCas9 | rAPOBEC1 | NGG | 1× | 4×UGI | - | 4-8 |
eA3A-BE3[ | nCas9 | hAPOBEC3A | TCR | 1× | 1×UGI | - | 7-12 |
BE4max[ | nCas9 | rAPOBEC1 | NGG | 2× | 2×UGI | - | 4-8 |
AncBE4max[ | nCas9 | rAPOBEC1 | NGG | 2× | 2×UGI | + | 4-8 |
FNLS-BE3[ | nCas9 | rAPOBEC1 | NGG | 2× | 1×UGI | + | 3-8 |
hyBE4max[ | nCas9 | rAPOBEC1 | NGG | 2× | 2×UGI 1×Rad51DBD | - | 4-12 |
hyA3A-BE4max[ | nCas9 | hA3A | TCR | 2× | 2×UGI 1×Rad51DBD | + | 3-15 |
YE1-BE3[ | nCas9 | rAPOBEC1-YE1 | NGG | 1× | 1×UGI | - | 4-7 |
YE2-BE3[ | nCas9 | rAPOBEC1-YE2 | NGG | 1× | 1×UGI | - | 5-6 |
YEE-BE3[ | nCas9 | rAPOBEC1-YEE | NGG | 1× | 1×UGI | - | 5-6 |
EE-BE3[ | nCas9 | rAPOBEC1-EE | NGG | 1× | 1×UGI | - | 5-5 |
CP-CBEmax[ | nCas9 | rAPOBEC1 | NGG | 1× | 2×UGI | - | 4-11 |
SaBE3[ | nSaCas9 | rAPOBEC1 | NNGRRT | 1× | 1×UGI | - | 3-12 |
VQR-BE3[ | VQR-Cas9nCas9 | rAPOBEC1 | NGA | 1× | 1×UGI | - | 4-11 |
EQR-BE3[ | EQR-Cas9nCas9 | rAPOBEC1 | NGAG | 1× | 1×UGI | - | 4-11 |
VRER-BE3[ | VRER-Cas9nCas9 | rAPOBEC1 | NGCG | 1× | 1×UGI | - | 3-10 |
SaKKH-BE3[ | nSaKKHCas9 | rAPOBEC1 | NNNRRT | 1× | 1×UGI | - | 3-12 |
XBT3[ | nxCas9 | rAPOBEC1 | NG/GAA/GAT | 1× | 1×UGI | - | 4-8 |
SpCas9-NG[ | nSpCas9-NG | rAPOBEC1 | NG | 1× | 1×UGI | - | 4-8 |
dCpf1-BE[ | dCpf1(Cas12a) | rAPOBEC1 | TTTV | 3× | 4×UGI | - | 8-13 |
enCas12a-A3A-Y130F[ | LbCas12a | hA3A | NTTN/TYCN/TRTV | 1× | 1×UGI | + | 7-12 |
RR-A3A-Y130F[ | LbCas12a | hA3A | NTTN/TYCN/TRTV | 1× | 1×UGI | + | 7-12 |
RVR-A3A-Y130F[ | LbCas12a | hA3A | NTTN/TYCN/TRTV | 1× | 1×UGI | + | 7-12 |
HF-BE3[ | HF1-nCas9 | rAPOBEC1 | NGG | 1× | 1×UGI | - | 4-8 |
TBEs[ | nCas9 | rAPOBEC1 | NGG | 1× | 1×UGI 1×dCDI | - | 4-8 |
SpG-CBE[ | SpG | rAPOBEC1 | NGN | 1× | 1×UGI | - | 4-8 |
SpRY-CBE[ | SpRY | rAPOBEC1 | NRN | 1× | 1×UGI | - | 4-8 |
ABE7.10[ | nCas9 | TadA-TadA* | NGG | 1× | - | - | 4-7 |
ABEmax[ | nCas9 | TadA-TadA* | NGG | 2× | - | + | 4-7 |
CP-ABEmax[ | CP-nCas9 | TadA-TadA* | NGG | 2× | - | + | 4-12 |
ABEmaxAW[ | nCas9 | TadA-E59A-TadA*-V106W | NGG | 2× | - | + | 4-8 |
ABEmaxQW[ | nCas9 | TadA-E59Q-TadA*-V106W | NGG | 2× | - | + | 4-8 |
ABE7.10D53E[ | nCas9 | TadA-D53E-TadA*-D53E | NGG | 1× | - | - | 4-8 |
ABE7.10F148A[ | nCas9 | TadA-F148A-TadA*-F148A | NGG | 1× | - | - | 5 |
VQR-SpCas9-ABEmax[ | nVQR-SpCas9 | TadA-TadA* | NGA | 2× | - | + | 4-8 |
VRER-SpCas9-ABEmax[ | nVRER-SpCas9 | TadA-TadA* | NGCG | 2× | - | + | 4-8 |
VRQR-SpCas9-ABEmax[ | nVRQR-SpCas9 | TadA-TadA* | NGA | 2× | - | + | 4-8 |
SaABEmax[ | nSaCas9 | TadA-TadA* | NNGRRT | 2× | - | + | 4-14 |
SaKKH-ABEmax[ | nSaKKH | TadA-TadA* | NNNRRT | 2× | - | + | 4-14 |
ScCas9-ABE7.10[ | nScCas9 | TadA-TadA* | NNGN | 1× | - | - | 4-7 |
xABEmax[ | nxCas9 | TadA-TadA* | NG | 2× | + | 4-8 | |
ABE-NG-S[ | SpCas9-NG | TadA* | NG | 1× | - | + | 4-7 |
SpG-ABEmax[ | SpG | TadA-TadA* | NGN | 2× | - | - | 4-7 |
SpRY-ABEmax[ | SpRY | TadA-TadA* | NRN | 2× | - | - | 4-7 |
ABE8e[ | nCas9 | TadA | NGG | 1× | - | - | 3-11 |
ABE8eV106W[ | nCas9 | TadA-V106W | NGG | 1× | - | - | 8-12 |
enCas12a-ABE8eV106W[ | LbCas12a | TadA-V106W | TTTV | 1× | - | + | 8-12 |
RR-ABE8eV106W[ | LbCas12a | TadA-V106W | TTTV | 1× | - | + | 8-12 |
RVR- ABE8eV106W[ | LbCas12a | TadA-V106W | TTTV | 1× | - | + | 8-12 |
TALE-ABE[ | TALE | TadA-F148A-TadA*-F148A | less | 1× | - | - | - |
TALE-CBE[ | nCas9 | rAPOBEC1-YE1 | less | 1× | 1×UGI | - | - |
GBE[ | nCas9 | rAPOBEC1 | NGG | 1× | 1×eUNG | - | 4-8 |
OPTI-CGBE[ | nCas9 | rAPOBEC1 | WCW | 1× | 1×UNG | + | 4-7 |
eA3A-OPTI-CGBEs[ | nCas9 | APOBEC3A | TCN | 1× | 1×UNG | + | 4-7 |
hA3G-OPTI-CGBEs[ | nCas9 | APOBEC3G | CCN | 1× | 1×UNG | + | 4-7 |
hA3G-CTD-OPTI-CGBEs[ | nCas9 | APOBEC3G | CCN | 1× | 1×UNG | + | 4-7 |
AYBEv0.1[ | nCas9 | TadA | NGG | 1× | 1×MPG | + | 3-11 |
AYBEv0.2[ | nCas9 | TadA | NGG | 1× | 1×MPG | + | 3-11 |
AYBEv0.3[ | nCas9 | TadA | NGG | 1× | 1×MPG | + | 3-11 |
Table 1 Characteristics of each base editor
名称 Name | Cas蛋白 Cas protein | 工具酶 Tool enzyme | PAM序列 PAM sequence | NLS | 附加原件 Additional original | 密码子优化 Codon optimiz-ation | 编辑窗口 Editing window |
---|---|---|---|---|---|---|---|
BE1[ | dCas9 | rAPOBEC1 | NGG | 1× | - | - | 4-8 |
BE2[ | dCas9 | rAPOBEC1 | NGG | 1× | 1×UGI | - | 4-8 |
BE3[ | nCas9 | rAPOBEC1 | NGG | 1× | 1×UGI | - | 4-8 |
BE3-R33A[ | nCas9 | rAPOBEC1R33A | NGG | 1× | 1×UGI | - | 5-7 |
BE3-R33A/K34A[ | nCas9 | rAPOBEC1R33A/K34A | NGG | 1× | 1×UGI | - | 5-6 |
Target-AID[ | nCas9 | PmCDA1 | NGG | 1× | 1×UGI | - | 2-8 |
TAM[ | dCas9 | hAIDx | NGG | 1× | 1×UGI | - | 4-10 |
CRISPR-X[ | dCas9 | hAIDΔ-MS2 | NGG | 1× | - | - | -50-50 |
ZF-hAID[ | ZF | hAID | less | 1× | 1×UGI | - | - |
TALE-hAID[ | TALE | hAID | less | 1× | 1×UGI | - | - |
BE4[ | nCas9 | rAPOBEC1 | NGG | 1× | 2×UGI | - | 4-8 |
BE4Gam[ | nCas9 | rAPOBEC1 | NGG | 1× | 2×UGI 1×Gam | - | 4-8 |
eBE[ | nCas9 | rAPOBEC1 | NGG | 1× | 4×UGI | - | 4-8 |
eA3A-BE3[ | nCas9 | hAPOBEC3A | TCR | 1× | 1×UGI | - | 7-12 |
BE4max[ | nCas9 | rAPOBEC1 | NGG | 2× | 2×UGI | - | 4-8 |
AncBE4max[ | nCas9 | rAPOBEC1 | NGG | 2× | 2×UGI | + | 4-8 |
FNLS-BE3[ | nCas9 | rAPOBEC1 | NGG | 2× | 1×UGI | + | 3-8 |
hyBE4max[ | nCas9 | rAPOBEC1 | NGG | 2× | 2×UGI 1×Rad51DBD | - | 4-12 |
hyA3A-BE4max[ | nCas9 | hA3A | TCR | 2× | 2×UGI 1×Rad51DBD | + | 3-15 |
YE1-BE3[ | nCas9 | rAPOBEC1-YE1 | NGG | 1× | 1×UGI | - | 4-7 |
YE2-BE3[ | nCas9 | rAPOBEC1-YE2 | NGG | 1× | 1×UGI | - | 5-6 |
YEE-BE3[ | nCas9 | rAPOBEC1-YEE | NGG | 1× | 1×UGI | - | 5-6 |
EE-BE3[ | nCas9 | rAPOBEC1-EE | NGG | 1× | 1×UGI | - | 5-5 |
CP-CBEmax[ | nCas9 | rAPOBEC1 | NGG | 1× | 2×UGI | - | 4-11 |
SaBE3[ | nSaCas9 | rAPOBEC1 | NNGRRT | 1× | 1×UGI | - | 3-12 |
VQR-BE3[ | VQR-Cas9nCas9 | rAPOBEC1 | NGA | 1× | 1×UGI | - | 4-11 |
EQR-BE3[ | EQR-Cas9nCas9 | rAPOBEC1 | NGAG | 1× | 1×UGI | - | 4-11 |
VRER-BE3[ | VRER-Cas9nCas9 | rAPOBEC1 | NGCG | 1× | 1×UGI | - | 3-10 |
SaKKH-BE3[ | nSaKKHCas9 | rAPOBEC1 | NNNRRT | 1× | 1×UGI | - | 3-12 |
XBT3[ | nxCas9 | rAPOBEC1 | NG/GAA/GAT | 1× | 1×UGI | - | 4-8 |
SpCas9-NG[ | nSpCas9-NG | rAPOBEC1 | NG | 1× | 1×UGI | - | 4-8 |
dCpf1-BE[ | dCpf1(Cas12a) | rAPOBEC1 | TTTV | 3× | 4×UGI | - | 8-13 |
enCas12a-A3A-Y130F[ | LbCas12a | hA3A | NTTN/TYCN/TRTV | 1× | 1×UGI | + | 7-12 |
RR-A3A-Y130F[ | LbCas12a | hA3A | NTTN/TYCN/TRTV | 1× | 1×UGI | + | 7-12 |
RVR-A3A-Y130F[ | LbCas12a | hA3A | NTTN/TYCN/TRTV | 1× | 1×UGI | + | 7-12 |
HF-BE3[ | HF1-nCas9 | rAPOBEC1 | NGG | 1× | 1×UGI | - | 4-8 |
TBEs[ | nCas9 | rAPOBEC1 | NGG | 1× | 1×UGI 1×dCDI | - | 4-8 |
SpG-CBE[ | SpG | rAPOBEC1 | NGN | 1× | 1×UGI | - | 4-8 |
SpRY-CBE[ | SpRY | rAPOBEC1 | NRN | 1× | 1×UGI | - | 4-8 |
ABE7.10[ | nCas9 | TadA-TadA* | NGG | 1× | - | - | 4-7 |
ABEmax[ | nCas9 | TadA-TadA* | NGG | 2× | - | + | 4-7 |
CP-ABEmax[ | CP-nCas9 | TadA-TadA* | NGG | 2× | - | + | 4-12 |
ABEmaxAW[ | nCas9 | TadA-E59A-TadA*-V106W | NGG | 2× | - | + | 4-8 |
ABEmaxQW[ | nCas9 | TadA-E59Q-TadA*-V106W | NGG | 2× | - | + | 4-8 |
ABE7.10D53E[ | nCas9 | TadA-D53E-TadA*-D53E | NGG | 1× | - | - | 4-8 |
ABE7.10F148A[ | nCas9 | TadA-F148A-TadA*-F148A | NGG | 1× | - | - | 5 |
VQR-SpCas9-ABEmax[ | nVQR-SpCas9 | TadA-TadA* | NGA | 2× | - | + | 4-8 |
VRER-SpCas9-ABEmax[ | nVRER-SpCas9 | TadA-TadA* | NGCG | 2× | - | + | 4-8 |
VRQR-SpCas9-ABEmax[ | nVRQR-SpCas9 | TadA-TadA* | NGA | 2× | - | + | 4-8 |
SaABEmax[ | nSaCas9 | TadA-TadA* | NNGRRT | 2× | - | + | 4-14 |
SaKKH-ABEmax[ | nSaKKH | TadA-TadA* | NNNRRT | 2× | - | + | 4-14 |
ScCas9-ABE7.10[ | nScCas9 | TadA-TadA* | NNGN | 1× | - | - | 4-7 |
xABEmax[ | nxCas9 | TadA-TadA* | NG | 2× | + | 4-8 | |
ABE-NG-S[ | SpCas9-NG | TadA* | NG | 1× | - | + | 4-7 |
SpG-ABEmax[ | SpG | TadA-TadA* | NGN | 2× | - | - | 4-7 |
SpRY-ABEmax[ | SpRY | TadA-TadA* | NRN | 2× | - | - | 4-7 |
ABE8e[ | nCas9 | TadA | NGG | 1× | - | - | 3-11 |
ABE8eV106W[ | nCas9 | TadA-V106W | NGG | 1× | - | - | 8-12 |
enCas12a-ABE8eV106W[ | LbCas12a | TadA-V106W | TTTV | 1× | - | + | 8-12 |
RR-ABE8eV106W[ | LbCas12a | TadA-V106W | TTTV | 1× | - | + | 8-12 |
RVR- ABE8eV106W[ | LbCas12a | TadA-V106W | TTTV | 1× | - | + | 8-12 |
TALE-ABE[ | TALE | TadA-F148A-TadA*-F148A | less | 1× | - | - | - |
TALE-CBE[ | nCas9 | rAPOBEC1-YE1 | less | 1× | 1×UGI | - | - |
GBE[ | nCas9 | rAPOBEC1 | NGG | 1× | 1×eUNG | - | 4-8 |
OPTI-CGBE[ | nCas9 | rAPOBEC1 | WCW | 1× | 1×UNG | + | 4-7 |
eA3A-OPTI-CGBEs[ | nCas9 | APOBEC3A | TCN | 1× | 1×UNG | + | 4-7 |
hA3G-OPTI-CGBEs[ | nCas9 | APOBEC3G | CCN | 1× | 1×UNG | + | 4-7 |
hA3G-CTD-OPTI-CGBEs[ | nCas9 | APOBEC3G | CCN | 1× | 1×UNG | + | 4-7 |
AYBEv0.1[ | nCas9 | TadA | NGG | 1× | 1×MPG | + | 3-11 |
AYBEv0.2[ | nCas9 | TadA | NGG | 1× | 1×MPG | + | 3-11 |
AYBEv0.3[ | nCas9 | TadA | NGG | 1× | 1×MPG | + | 3-11 |
Fig. 2 Mechanisms of prime editors Having PE2 as an example, the base editor is composed of important components PE2 protein(nCas9(H840A)+RTase)and pegRNA(sgRNA+RTT+PBS). sgRNA and nCas9(H840A)recognize specific DNA sequences and cut single strands. RTT and PBS provide reverse transcription binding sites and reverse transcription templates. After DNA replication and repair mechanisms, target targets are finally targeted for modification
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