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狒狒肾脏转录组:转录序列、剪接变异体和丰度分析。

The baboon kidney transcriptome: analysis of transcript sequence, splice variants, and abundance.

机构信息

Department of Genetics, Texas Biomedical Research Institute, San Antonio, Texas, United States of America.

出版信息

PLoS One. 2013 Apr 23;8(4):e57563. doi: 10.1371/journal.pone.0057563. Print 2013.

DOI:10.1371/journal.pone.0057563
PMID:23637735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3634053/
Abstract

The baboon is an invaluable model for the study of human health and disease, including many complex diseases of the kidney. Although scientists have made great progress in developing this animal as a model for numerous areas of biomedical research, genomic resources for the baboon, such as a quality annotated genome, are still lacking. To this end, we characterized the baboon kidney transcriptome using high-throughput cDNA sequencing (RNA-Seq) to identify genes, gene variants, single nucleotide polymorphisms (SNPs), insertion-deletion polymorphisms (InDels), cellular functions, and key pathways in the baboon kidney to provide a genomic resource for the baboon. Analysis of our sequencing data revealed 45,499 high-confidence SNPs and 29,813 InDels comparing baboon cDNA sequences with the human hg18 reference assembly and identified 35,900 cDNAs in the baboon kidney, including 35,150 transcripts representing 15,369 genic genes that are novel for the baboon. Gene ontology analysis of our sequencing dataset also identified numerous biological functions and canonical pathways that were significant in the baboon kidney, including a large number of metabolic pathways that support known functions of the kidney. The results presented in this study catalogues the transcribed mRNAs, noncoding RNAs, and hypothetical proteins in the baboon kidney and establishes a genomic resource for scientists using the baboon as an experimental model.

摘要

狒狒是研究人类健康和疾病的宝贵模型,包括许多肾脏的复杂疾病。尽管科学家们在将这种动物开发为许多生物医学研究领域的模型方面取得了巨大进展,但狒狒的基因组资源,如质量注释基因组,仍然缺乏。为此,我们使用高通量 cDNA 测序(RNA-Seq)来描述狒狒肾脏转录组,以鉴定狒狒肾脏中的基因、基因变体、单核苷酸多态性(SNP)、插入缺失多态性(InDel)、细胞功能和关键途径,为狒狒提供基因组资源。我们的测序数据分析表明,与人类 hg18 参考组装相比,狒狒 cDNA 序列中有 45499 个高可信度 SNP 和 29813 个 InDel,并在狒狒肾脏中鉴定出 35900 个 cDNA,包括 35150 个代表 15369 个基因的转录本,这些基因对于狒狒来说是新的。我们测序数据集的基因本体分析还确定了许多在狒狒肾脏中具有重要意义的生物学功能和经典途径,包括许多支持肾脏已知功能的代谢途径。本研究的结果列出了狒狒肾脏中的转录 mRNA、非编码 RNA 和假设蛋白,并为使用狒狒作为实验模型的科学家建立了基因组资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b502/3634053/9bfe4da3c5a9/pone.0057563.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b502/3634053/53f503bd551d/pone.0057563.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b502/3634053/9bfe4da3c5a9/pone.0057563.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b502/3634053/53f503bd551d/pone.0057563.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b502/3634053/9bfe4da3c5a9/pone.0057563.g002.jpg

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