Yuan Xiu-Xiu, Wang Yu
Center of Reproductive Medicine, The Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia 010000, China.
Department of Reproductive Medicine, Datong Third People's Hospital, Datong, Shanxi 037000, China.
Zhonghua Nan Ke Xue. 2024 Feb;30(2):111-117.
To investigate the effect of miR-199b-5p knockout on the expression of the CREM gene in the semen and testis of mice.
We selected 8 miR-199b-5p knockout (KO) male mice (the KO group) and another 8 wild-type (WT) C57BL/6 male mice (the WT group), and observed the changes in their body weight, testicular index, testis structure and sperm morphology. We detected sperm concentration under the microscope, determined the mRNA and protein expression levels of CREM in the semen and testis by RT-qPCR and Western blot respectively, and predicted the targeting relationship between CREM and miR-199b-5p using the online database.
There were no significant changes in the body weight and testicular index in either of the two groups. Compared with the WT mice, the animals in the KO group showed a slight reduction in both the count and concentration of sperm (P>0.05). Testis pathology exhibited a lower testis volume in the KO than in the WT mice, but no obvious abnormalities in the testis tissue, spermatogenic and supporting cells in the seminiferous tubules, boundary membrane or diameter of the seminiferous tubule. Online database prediction indicated that CREM was the target gene of miR-199b-5p. Both the mRNA and protein expressions of CREM in the semen and testis of the mice were significantly decreased in the KO group compared with those in the WT group (both P<0.05). A six-month follow-up showed a remarkably lower rate of male births in the KO than in the WT mice (P<0.05).
The expression of the CREM gene is down-regulated in the semen and testis of miR-199b-5p knockout male mice, and miR-199b-5p may affect the fertility of male mice by targeting CREM.
探讨miR-199b-5p基因敲除对小鼠精液及睾丸中CREM基因表达的影响。
选取8只miR-199b-5p基因敲除(KO)雄性小鼠作为基因敲除组,另选8只野生型(WT)C57BL/6雄性小鼠作为野生型组,观察两组小鼠体重、睾丸指数、睾丸结构及精子形态的变化。显微镜下检测精子浓度,分别采用RT-qPCR和蛋白质免疫印迹法检测精液及睾丸中CREM基因的mRNA和蛋白质表达水平,并利用在线数据库预测CREM与miR-199b-5p的靶向关系。
两组小鼠体重及睾丸指数均无明显变化。与野生型小鼠相比,基因敲除组小鼠精子数量和浓度略有降低(P>0.05)。睾丸病理学检查显示,基因敲除组小鼠睾丸体积较野生型小鼠小,但睾丸组织、生精小管中的生精细胞和支持细胞、界膜或生精小管直径均无明显异常。在线数据库预测表明,CREM是miR-199b-5p的靶基因。与野生型组相比,基因敲除组小鼠精液及睾丸中CREM基因的mRNA和蛋白质表达均显著降低(均P<0.05)。6个月的随访结果显示,基因敲除组雄鼠出生率显著低于野生型组(P<0.05)。
miR-199b-5p基因敲除雄性小鼠精液及睾丸中CREM基因表达下调,miR-199b-5p可能通过靶向作用于CREM影响雄性小鼠生育能力。