SRSF1 inhibits HBV replication by enhancing the stability of P53 in cell models
Basic Medicine|更新时间:2025-07-14
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SRSF1 inhibits HBV replication by enhancing the stability of P53 in cell models
Journal of Army Medical UniversityVol. 47, Issue 13, Pages: 1475-1483(2025)
作者机构:
1.重庆医科大学感染性疾病分子生物学教育部重点实验室,重庆
2.空军军医大学第一附属医院,陕西西安
作者简介:
CUI Jing, E-mail: cuijing@cqmu.edu.cn
基金信息:
the General Program of National Natural Science Foundation of China(82470634);the Key Scientific and technological Research Project of Chongqing Education Commission(KJZD-K202200409)
LIU J J,LONG S Y,HU J L,et al.SRSF1 inhibits HBV replication by enhancing the stability of P53 in cell models[J].J Army Med Univ,2025,47(13):1475-1483.DOI:10.16016/j.2097-0927.202503083.
LIU J J,LONG S Y,HU J L,et al.SRSF1 inhibits HBV replication by enhancing the stability of P53 in cell models[J].J Army Med Univ,2025,47(13):1475-1483.DOI:10.16016/j.2097-0927.202503083.DOI:
SRSF1 inhibits HBV replication by enhancing the stability of P53 in cell models
Objective To investigate the effect and underlying mechanism of serine and arginine rich splicing factor 1 (SRSF1) on the replication of hepatitis B virus (HBV). Methods The effects of SRSF1 on HBV replication were investigated in different HBV replicating cell models by Southern blotting
Northern blotting and ELISA. Quantitative PCR
luciferase reporter assay and chromatin immunoprecipitation (ChIP) were applied to dete
rmine the effects of SRSF1 on the activities of HBV core promoter/enhancer in HepG2 cells. The relationship between SRSF1 and P53 was explored with Western blotting and ubiquitination assay. The effects of P53 on HBV replication were verified in different HBV replicating cell models
and the role of P53 in SRSF1 inhibition of HBV was clarified. Results Overexpression of SRSF1 significantly inhibited HBV DNA and HBV RNA and reduced HBsAg and HBeAg secretion levels in a variety of HBV replicative cell models (
P
<
0.0001). SRSF1 also inhibited the activity of HBV core promoter
although this inhibition was regulated by indirect mechanisms. In addition
SRSF1 enhanced P53 stability by protecting P53 from ubiquitination and subsequent proteasomal degradation. Meanwhile
the regulatory effect of overexpression or knockdown of P53 on HBV was validated in different cell models (
P
<
0.0001). Conclusion Overexpression of splicing factor SRSF1 significantly inhibits HBV replication in a variety of cell models
and this inhibitory effect is mediated by its enhancement of P53 stability.
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references
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