Effective inhibition of human cytomegalovirus UL148 gene expression by external guide sequences in vitro
10.3760/cma.j.issn.1003-9279.2017.03.001
- VernacularTitle: 应用外部引导序列切割人巨细胞病毒UL148 RNA的研究
- Author:
Jingjing HU
1
;
Bo WANG
;
Haihao SU
;
Juncai DING
;
Yuanyuan GUO
;
Binhua XIE
;
Yuanbin WU
;
Lijun CAI
;
Mengjie GUO
Author Information
1. Department of Pediatrics, Guangdong Provincial Maternal and Child Health Hospital, Guangzhou 511442, China
- Publication Type:Journal Article
- Keywords:
Human cytomegalovirus;
External guide sequences;
UL148;
Clinic isolate
- From:
Chinese Journal of Experimental and Clinical Virology
2017;31(3):185-188
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To investigate the UL148 gene function of human cytomegalovirus (HCMV) low passage clinic isolate and new strategies for anti-HCMV treatment, the DNA-based external guide sequences (EGSs) were designed to inhibit UL148 RNA expression.
Methods:UL148 RNA secondary structure was analyzed by RNA structure technique, an appropriate region was chosen for DNA-based EGS57 synthesis, targeted the UL148 RNA. The M1RNA and UL148 RNA were generated by PCR for transcription in vitro. The UL148 RNA and M1RNA were transcribed in vitro under the function of T7 RNA polymerase. The UL148 was labelled by 32P. The cleavage reactions were carried out by mixing up EGS, M1RNA with UL148 RNA for 1 h. The products were separated by urea denaturing polyacrylamide gel electrophoresis and detected with Typhoon Phosphor Imager.
Results:UL148 RNA ranged from 58 to 72 sites was the binding position, and 57 was a cleavage site. EGS57 was designed and synthesized. EGS57 was combined with UL148 RNA to form the natural substrate of M1RNA. UL148 RNA and M1RNA were synthesized through T7 RNA polymerase catalyzing, and the products were conformed. After cleaving reactions, DNA-based EGS57 was shown to be able to cleave UL148 RNA efficiently in vitro by a complex with M1RNA.
Conclusions:UL148 RNA was cleaved efficiently by EGS57, and the cleaving site was conformed as expectation. It will provide the gene silent tool effectively for further study the function of UL148 gene.
