首页|鸡SLMO2基因CDS区克隆、生物信息学及组织表达分析

鸡SLMO2基因CDS区克隆、生物信息学及组织表达分析

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为了探究类果蝇慢移基因的氨基酸序列特征,探索其在不同肤色鸡不同组织中mRNA表达变化规律,实验采集不同肤色鸡各组织,PCR克隆获得SLMO2完整CDS区,进行生物信息学分析及组织表达分析。实验得到SLMO2的CDS区序列全长 560 bp,其中可编码氨基酸 174 个。生物信息学研究结果表明,鸡SLMO2蛋白并不具有信号肽和跨膜结构,蛋白主要结构以无规性卷曲的α-螺旋结构结合为主,且蛋白分布在线粒体内膜间隙。通过氨基酸序列对比发现,鸡与爪蟾的亲缘关系较近。qRT-PCR结果表明,SLMO2在背肤组织中相对表达量极显著高于其他组织,且该基因在丝羽乌骨鸡背肤组织中表达量极显著高于"豫粉1号"H系鸡。以上结果为进一步探究鸡SLMO2对黑色素沉积的调控机制提供了理论依据。
Cloning,Expression and Bioinformatics Analysis of the CDS Region of Chicken SLMO2 Gene
This study is to investigate the amino acid sequence characteristics of drosophila-like slow-moving gene and its mRNA expression in different tissues of chicken with different skin colors.The CDS sequence of SLMO2 with a total length of 560 bp was cloned by PCR,and it encoded 174 amino acids.The bioinformatics analyses showed that there were no transmembrane structures and signal peptides in the chicken SLMO2 protein,and the protein structure was mainly composed of irregular curly and α-spiral structures,and it was distributed in the mitochondrial inner membrane space.Amino acid sequence comparison showed that the genetic relationship between chicken and Xenopus was close.qRT-PCR assay showed that the expression level of SLMO2 in the back skin tissue of Silkie was significantly higher than that of other tissues(P<0.01),and the expression level of SLMO2 in the back skin tissue of yellow-feather chicken was significantly higher than that in other tissues(P<0.01).The above results will provide a theoretical basis for further study on the regulatory mechanism of chicken SLMO2 gene in melanin deposition.

ChickenSLMO2 geneCDS region cloningExpression analysisBioinformatics analysis

朱慧媛、张朋威、徐硕辉、李瑞婷、高超群、李文婷、蒋瑞瑞、孙桂荣、韩瑞丽、康相涛、李东华

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河南农业大学动物科技学院,河南郑州 450046

河南省家禽种质资源创新与利用重点实验室,河南郑州 450046

SLMO2基因 CDS区克隆 组织表达 生物信息学分析

河南省自然科学基金青年项目国家自然科学基金中原学者首席科学家工作室

2023004102033210254030601985

2024

中国畜牧杂志
中国畜牧兽医学会

中国畜牧杂志

CSTPCD北大核心
影响因子:0.704
ISSN:0258-7033
年,卷(期):2024.60(2)
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