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首页> 外文期刊>International Journal of Genomics >Identification of Putative Ortholog Gene Blocks Involved in Gestant and Lactating Mammary Gland Development: A Rodent Cross-Species Microarray Transcriptomics Approach
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Identification of Putative Ortholog Gene Blocks Involved in Gestant and Lactating Mammary Gland Development: A Rodent Cross-Species Microarray Transcriptomics Approach

机译:假定的直向同源基因块参与的动物和乳腺发育的鉴定:啮齿类动物跨物种微阵列转录组学方法。

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摘要

The mammary gland (MG) undergoes functional and metabolic changes during the transition from pregnancy to lactation, possibly by regulation of conserved genes. The objective was to elucidate orthologous genes, chromosome clusters and putative conserved transcriptional modules during MG development. We analyzed expression of 22,000 transcripts using murine microarrays and RNA samples of MG from virgin, pregnant, and lactating rats by cross-species hybridization. We identified 521 transcripts differentially expressed; upregulated in early (78%) and midpregnancy (89%) and early lactation (64%), but downregulated in mid-lactation (61%). Putative orthologous genes were identified. We mapped the altered genes to orthologous chromosomal locations in human and mouse. Eighteen sets of conserved genes associated with key cellular functions were revealed and conserved transcription factor binding site search entailed possible coregulation among all eight block sets of genes. This study demonstrates that the use of heterologous array hybridization for screening of orthologous gene expression from rat revealed sets of conserved genes arranged in chromosomal order implicated in signaling pathways and functional ontology. Results demonstrate the utilization power of comparative genomics and prove the feasibility of using rodent microarrays to identification of putative coexpressed orthologous genes involved in the control of human mammary gland development.
机译:乳腺(MG)在从妊娠到哺乳的过渡过程中可能会发生功能和代谢变化,这可能是通过保守基因的调控引起的。目的是阐明MG发育过程中的直系同源基因,染色体簇和假定的保守转录模块。我们通过跨物种杂交,使用鼠源微阵列和来自原始,妊娠和哺乳期大鼠的MG的RNA样品分析了22,000个转录本的表达。我们鉴定了521个差异表达的转录本;在早期(78%)和中期妊娠(89%)和早期哺乳期(64%)上调,但在哺乳中期(61%)下调。确定推定的直系同源基因。我们将改变的基因定位到人类和小鼠的直系同源染色体位置。揭示了18个与关键细胞功能相关的保守基因,保守的转录因子结合位点搜索需要在所有8个基因组之间进行可能的调控。这项研究表明,使用异源阵列杂交从大鼠中筛选直系同源基因表达,揭示了以染色体顺序排列的保守基因集,涉及信号通路和功能本体。结果证明了比较基因组学的利用能力,并证明了使用啮齿类动物微阵列鉴定参与控制人类乳腺发育的假定共表达直系同源基因的可行性。

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