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具有不同关节炎、自身免疫、炎症和癌症易感性的 DA 和 F344 大鼠的全基因组序列。

Whole-genome sequences of DA and F344 rats with different susceptibilities to arthritis, autoimmunity, inflammation and cancer.

机构信息

BGI-Shenzhen, Shenzhen 518083, China.

出版信息

Genetics. 2013 Aug;194(4):1017-28. doi: 10.1534/genetics.113.153049. Epub 2013 May 20.

Abstract

DA (D-blood group of Palm and Agouti, also known as Dark Agouti) and F344 (Fischer) are two inbred rat strains with differences in several phenotypes, including susceptibility to autoimmune disease models and inflammatory responses. While these strains have been extensively studied, little information is available about the DA and F344 genomes, as only the Brown Norway (BN) and spontaneously hypertensive rat strains have been sequenced to date. Here we report the sequencing of the DA and F344 genomes using next-generation Illumina paired-end read technology and the first de novo assembly of a rat genome. DA and F344 were sequenced with an average depth of 32-fold, covered 98.9% of the BN reference genome, and included 97.97% of known rat ESTs. New sequences could be assigned to 59 million positions with previously unknown data in the BN reference genome. Differences between DA, F344, and BN included 19 million positions in novel scaffolds, 4.09 million single nucleotide polymorphisms (SNPs) (including 1.37 million new SNPs), 458,224 short insertions and deletions, and 58,174 structural variants. Genetic differences between DA, F344, and BN, including high-impact SNPs and short insertions and deletions affecting >2500 genes, are likely to account for most of the phenotypic variation between these strains. The new DA and F344 genome sequencing data should facilitate gene discovery efforts in rat models of human disease.

摘要

DA(棕褐色血的棕榈和野猪鼠,也称为暗棕褐色)和 F344(Fisher)是两个近交系大鼠品系,在几个表型上存在差异,包括对自身免疫疾病模型和炎症反应的易感性。虽然这些品系已经被广泛研究,但关于 DA 和 F344 基因组的信息很少,因为迄今为止只有棕色挪威(BN)和自发性高血压大鼠品系被测序。在这里,我们使用下一代 Illumina 配对末端读取技术报告了 DA 和 F344 基因组的测序,并首次从头组装了大鼠基因组。DA 和 F344 的测序深度平均为 32 倍,覆盖了 BN 参考基因组的 98.9%,并包含了 97.97%的已知大鼠 ESTs。新序列可以分配到 BN 参考基因组中以前未知的数据的 5900 万个位置。DA、F344 和 BN 之间的差异包括新支架中的 1900 万个位置、409 万个单核苷酸多态性(SNP)(包括 137 万个新 SNP)、458224 个短插入和缺失以及 58174 个结构变异。DA、F344 和 BN 之间的遗传差异,包括影响>2500 个基因的高影响 SNP 和短插入和缺失,很可能解释了这些品系之间大多数表型变异的原因。新的 DA 和 F344 基因组测序数据应该有助于在人类疾病的大鼠模型中进行基因发现工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90e6/3730908/c187e070bd79/1017fig1.jpg

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