molecular cloning and gene expression analysis of ercc6l in sika deer (cervus nippon hortulorum)分子克隆和基因表达分析的ercc6l梅花鹿(cervus日本hortulorum).pdfVIP
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molecular cloning and gene expression analysis of ercc6l in sika deer (cervus nippon hortulorum)分子克隆和基因表达分析的ercc6l梅花鹿(cervus日本hortulorum)
Molecular Cloning and Gene Expression Analysis of Ercc6l in Sika Deer (Cervus nippon hortulorum) 1. 1,2. 1 1 1 Yupeng Yin , Lina Tang , Jiabao Zhang , Bo Tang *, Ziyi Li * 1Jilin Provincial Key Laboratory of Animal Embryo Engineering, The Center for Animal Embryo Engineering of Jilin Province, College of Animal Science and Veterinary Medicine, Jilin University, Changchun, Jilin, China, 2 Ministry of Education Key Laboratory of Enzyme Engineering, College of Life Sciences, Jilin University, Changchun, Jilin, China Abstract Background: One important protein family that functions in nucleotide excision repair (NER) factors is the SNF2 family. A newly identified mouse ERCC6-like gene, Ercc6l (excision repair cross-complementing rodent repair deficiency, complementation group 6-like), has been shown to be another developmentally related member of the SNF2 family. Methodology/Principal Findings: In this study, Sika deer Ercc6l cDNA was first cloned and then sequenced. The full-length cDNA of the Sika deer Ercc6l gene is 4197 bp and contains a 3732 bp open reading frame that encodes a putative protein of 1243 amino acids. The similarity of Sika deer Ercc6l to Bos taurus Ercc6l is 94.05% at the amino acid sequence level. The similarity, however, is reduced to 68.42–82.21% when compared to Ercc6l orthologs in other mammals and to less than 50% compared to orthologs in Gallus gallus and Xenopus. Additionally, the expression of Ercc6l mRNA was investigated in the organs of fetal and adult Sika deer (FSD and ASD, respectively) by quantitative RT-PCR. The common expression level of Ercc6l mRNA in the heart, liver, spleen, lung, kidney, and stomach from six different developmental stages of 18 Sika deer were examined, though the expression levels
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