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A 5′- Regulatory Region and Two Coding Region Polymorphisms Modulate Promoter Activity and Gene Expression of the Growth Suppressor Gene ZBED6 in Cattle

机译:5-调节区和两个编码区多态性调节牛生长抑制基因ZBED6的启动子活性和基因表达

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摘要

Zinc finger, BED-type containing 6 (ZBED6) is an important transcription factor in placental mammals, affecting development, cell proliferation and growth. Polymorphisms in its promoter and coding regions are likely to impact ZBED6 transcription and growth traits. In this study, rapid amplification of 5’ cDNA ends (5'-RACE) analysis revealed two transcription start sites (TSS) for the bovine ZBED6 starting within exon 1 of the ZC3H11A gene (TSS-1) and upstream of the translation start codon of the ZBED6 gene (TSS-2). There was one SNP in the promoter and two missense mutations in the coding region of the bovine ZBED6 by sequencing of the pooled DNA samples (Pool-Seq, n = 100). The promoter and coding region are the key regions for gene function; polymorphisms in these regions can alter gene expression. Quantitative real-time PCR (qPCR) analysis showed that ZBED6 has a broad tissue distribution in cattle and is highly expressed in skeletal muscle. Eleven promoter-detection vectors were constructed, which enabled the cloning of putative promoter sequences and analysis of ZBED6 transcriptional activity by luciferase reporter gene assays. The core region of the basal promoter of bovine ZBED6 is located within region -866 to -556. The activity of WT-826G-pGL3 in driving reporter gene transcription is significantly higher than that of the M-826A-pGL3 construct (P < 0.01). Analysis of gene expression patterns in homozygous full-sibling Chinese Qinchuan cattle showed that the mutant-type Hap-AGG exhibited a lower mRNA level than the wild-type Hap-GCA (P < 0.05) in longissimus dorsi muscle (LDM). Moreover, ZBED6 mRNA expression was low in C2C12 cells overexpressing the mutant-type ZBED6 (pcDNA3.1+-Hap-GG) (P < 0.01). Our results suggest that the polymorphisms in the promoter and coding regions may modulate the promoter activity and gene expression of bovine ZBED6 in the skeletal muscles of these cattle breeds.
机译:含BED型6的锌指(ZBED6)是胎盘哺乳动物中的重要转录因子,影响发育,细胞增殖和生长。其启动子和编码区的多态性可能影响ZBED6转录和生长性状。在这项研究中,对5'cDNA末端的快速扩增(5'-RACE)分析揭示了牛ZBED6的两个转录起始位点(TSS),起始于ZC3H11A基因外显子1(TSS-1),位于翻译起始密码子的上游ZBED6基因(TSS-2)的序列。通过对合并的DNA样品进行测序,在牛ZBED6的启动子中有一个SNP和两个错义突变(Pool-Seq,n = 100)。启动子和编码区是基因功能的关键区域。这些区域的多态性可以改变基因表达。实时荧光定量PCR(qPCR)分析表明ZBED6在牛中具有广泛的组织分布,并在骨骼肌中高表达。构建了11个启动子检测载体,该载体能够克隆假定的启动子序列,并通过荧光素酶报告基因分析对ZBED6转录活性进行分析。牛ZBED6的基础启动子的核心区域位于-866至-556区域。 WT-826G-pGL3在驱动报告基因转录中的活性显着高于M-826A-pGL3构建体(P <0.01)。对纯合子全同胞中国秦川牛的基因表达模式进行分析表明,在背最长肌中,突变型Hap-AGG的mRNA水平低于野生型Hap-GCA(P <0.05)。此外,在过表达突变型ZBED6(pcDNA3.1 + -Hap-GG)的C2C12细胞中,ZBED6 mRNA的表达较低(P <0.01)。我们的结果表明,启动子和编码区的多态性可能会调节这些牛品种骨骼肌中牛ZBED6的启动子活性和基因表达。

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