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鉴定参与妊娠和哺乳期乳腺发育的假定直系同源基因块:一种啮齿动物跨物种微阵列转录组学方法。

Identification of putative ortholog gene blocks involved in gestant and lactating mammary gland development: a rodent cross-species microarray transcriptomics approach.

机构信息

Unit of Medical Research in Nutrition, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Avenida Cuauhtémoc 330, Col. Doctores, Delegación Cuauhtémoc, 06725 Mexico City, Mexico.

出版信息

Int J Genomics. 2013;2013:624681. doi: 10.1155/2013/624681. Epub 2013 Oct 30.

Abstract

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.

摘要

乳腺(MG)在从妊娠到哺乳的过渡过程中经历功能和代谢变化,可能通过保守基因的调节。目的是阐明 MG 发育过程中的同源基因、染色体簇和推定的保守转录模块。我们使用鼠微阵列分析了 22000 个转录本的表达,并通过种间杂交分析了来自处女、妊娠和哺乳期大鼠的 MG 的 RNA 样本。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%)和早期泌乳(64%)上调,但在中期泌乳(61%)下调。鉴定了推定的同源基因。我们将改变的基因映射到人类和小鼠的同源染色体位置。揭示了与关键细胞功能相关的 18 组保守基因,保守转录因子结合位点搜索可能涉及所有 8 个基因块组之间的核心调控。这项研究表明,使用异源阵列杂交筛选大鼠的同源基因表达揭示了按染色体顺序排列的一组保守基因,这些基因参与信号通路和功能本体论。结果证明了比较基因组学的利用能力,并证明了使用啮齿动物微阵列鉴定参与人类乳腺发育调控的推定共表达同源基因的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/3830774/507cc9fc754b/IJG2013-624681.001.jpg

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