Suppr超能文献

褐鳟基因组中两个转铁蛋白基因座的证据。

Evidence for two transferrin loci in the Salmo trutta genome.

作者信息

Rozman T, Dovc P, Marić S, Kokalj-Vokac N, Erjavec-Skerget A, Rab P, Snoj A

机构信息

Department of Animal Science, University of Ljubljana, Groblje 3, SI-1230 DomZale, Slovenia.

出版信息

Anim Genet. 2008 Dec;39(6):577-85. doi: 10.1111/j.1365-2052.2008.01768.x. Epub 2008 Sep 11.

Abstract

To determine the organization of transferrin (TF) locus in the Salmo trutta genome, partial DNA and cDNA sequencing, fluorescent in situ hybridization (FISH) and Salmo salar BAC analysis were performed. TF expression levels and copy number prediction were assessed using real-time PCR. In addition to two previously reported DNA TF variant sequences of S. trutta and Salmo marmoratus (TF1), two novel variant sequences (TF2) were revealed in both species. Variant-specific sequence tags, characterizing two variants for each TF type (TF1 and TF2), were identified in genomic clones from each of the F1 hybrids between S. trutta and S. marmoratus. These clearly documented double heterozygote status at the TF loci. The real-time PCR data showed that each of the two TF types (TF1 and TF2) existed in one copy only and that the transcription of TF2 was considerably lower compared with TF1. Using FISH, hybridization signals were observed on two medium-sized acrocentric chromosomes of S. trutta karyotype. A TF type-specific PCR followed by a restriction analysis revealed the presence of two TF loci in the majority of analysed BAC clones. It was concluded that the TF gene is duplicated in the genome of S. trutta, and that the two TF loci are located adjacent to one another on the same chromosome. The differing transcription levels of TF1 and TF2 appear to depend on the corresponding promoter activity, which at least for TF2 seems to vary between different Salmo congeners.

摘要

为确定褐鳟基因组中转铁蛋白(TF)基因座的组织情况,进行了部分DNA和cDNA测序、荧光原位杂交(FISH)以及大西洋鲑BAC分析。使用实时PCR评估TF表达水平和拷贝数预测。除了之前报道的褐鳟和大理石纹鳟(TF1)的两个DNA TF变异序列外,在这两个物种中还发现了两个新的变异序列(TF2)。在褐鳟和大理石纹鳟之间的每个F1杂种的基因组克隆中,鉴定出了针对每种TF类型(TF1和TF2)的两个变异体的变异体特异性序列标签。这些清楚地记录了TF基因座的双杂合子状态。实时PCR数据表明,两种TF类型(TF1和TF2)均仅以一个拷贝存在,并且与TF1相比,TF2的转录水平相当低。使用FISH,在褐鳟核型的两条中等大小的近端着丝粒染色体上观察到杂交信号。进行TF类型特异性PCR后进行限制性分析,结果显示在大多数分析的BAC克隆中存在两个TF基因座。得出的结论是,TF基因在褐鳟基因组中是重复的,并且两个TF基因座在同一条染色体上彼此相邻。TF1和TF2转录水平的差异似乎取决于相应的启动子活性,至少对于TF2而言,不同的鲑属同源物种之间的启动子活性似乎有所不同。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验