Liu Juan, Sun Yan, Yang Chunhong, Zhang Yan, Jiang Qiang, Huang Jinming, Ju Zhihua, Wang Xiuge, Zhong Jifeng, Wang Changfa
Dairy Cattle Research Center, Shandong Academy of Agricultural Science, Jinan, P. R. China.
College of Agronomic Sciences in Shandong Agricultural University, Taian, China.
PLoS One. 2016 Sep 26;11(9):e0162730. doi: 10.1371/journal.pone.0162730. eCollection 2016.
Inner centromere protein (INCENP) plays an important role in mitosis and meiosis as the main member of chromosomal passenger protein complex (CPC). To investigate the functional markers of the INCENP gene associated with semen quality, the single nucleotide polymorphisms (SNPs) g.19970 A>G and g.34078 T>G were identified and analyzed. The new splice variant INCENP-TV is characterized by the deletion of exon 12. The g.19970 A>G in the exonic splicing enhancer (ESE) motif region results in an aberrant splice variant by constructing two minigene expression vectors using the pSPL3 exon capturing vector and transfecting vectors into MLTC-1 cells. INCENP-TV was more highly expressed than INCENP-reference in adult bull testes. The g.34078 T>G located in the binding region of bta-miR-378 could affect the expression of INCENP, which was verified by luciferase assay. To analyze comprehensively the correlation of SNPs with sperm quality, haplotype combinations constructed by g.19970 A>G and g.34078 T>G, as well as g.-692 C>T and g.-556 G>T reported in our previous studies, were analyzed. The bulls with H1H12 and H2H2 exhibited a higher ejaculate volume than those with H2H10 and H9H12, respectively (P < 0.05). Bulls with H11H11 and H2H10 exhibited higher initial sperm motility than those with H2H2 (P < 0.05). The expression levels of INCENP in bulls with H1H12 and H11H11 were significantly higher than those in bulls with H9H12 (P < 0.05), as determined by qRT-PCR. Findings suggest that g.19970 A>G and g.34078 T>G in INCENP both of which appear to change the molecular and biological characteristics of the mRNA transcribed from the locus may serve as a biomarkers of male bovine fertility by affecting alternative splicing mode and binding affinity with the target bta-miR-378.
着丝粒内蛋白(INCENP)作为染色体乘客蛋白复合体(CPC)的主要成员,在有丝分裂和减数分裂中发挥着重要作用。为了研究与精液质量相关的INCENP基因功能标记,对单核苷酸多态性(SNP)g.19970 A>G和g.34078 T>G进行了鉴定和分析。新的剪接变体INCENP-TV的特征是外显子12缺失。通过使用pSPL3外显子捕获载体构建两个小基因表达载体并将其转染到MLTC-1细胞中,发现外显子剪接增强子(ESE)基序区域中的g.19970 A>G导致异常剪接变体。在成年公牛睾丸中,INCENP-TV的表达高于INCENP参考序列。位于bta-miR-378结合区域的g.34078 T>G可能影响INCENP的表达,荧光素酶测定法验证了这一点。为了全面分析SNP与精子质量的相关性,分析了由g.19970 A>G和g.34078 T>G以及我们先前研究中报道的g.-692 C>T和g.-556 G>T构建的单倍型组合。具有H1H12和H2H2的公牛射精量分别高于具有H2H10和H9H12的公牛(P<0.05)。具有H11H11和H2H10的公牛初始精子活力高于具有H2H2的公牛(P<0.05)。通过qRT-PCR测定,具有H1H12和H11H11的公牛中INCENP的表达水平显著高于具有H9H12的公牛(P<0.05)。研究结果表明,INCENP中的g.19970 A>G和g.34078 T>G似乎都改变了该基因座转录的mRNA的分子和生物学特性,它们可能通过影响可变剪接模式和与靶标bta-miR-378的结合亲和力,作为雄性牛生育能力的生物标志物。