Placental transcriptome co-expression analysis reveals conserved regulatory programs across gestation

被引:26
作者
Buckberry, Sam [1 ,2 ,3 ]
Bianco-Miotto, Tina [1 ,4 ]
Bent, Stephen J. [1 ]
Clifton, Vicki [1 ]
Shoubridge, Cheryl [1 ]
Shankar, Kartik [5 ]
Roberts, Claire T. [1 ]
机构
[1] Univ Adelaide, Robinson Res Inst, Sch Paediat & Reprod Hlth, Adelaide, SA 5005, Australia
[2] Univ Western Australia, Harry Perkins Inst Med Res, Perth, WA 6009, Australia
[3] Univ Western Australia, Australian Res Council Ctr Excellence Plant Energ, Perth, WA 6009, Australia
[4] Univ Adelaide, Sch Agr Food & Wine, Adelaide, SA 5005, Australia
[5] Univ Arkansas Med Sci, Dept Pediat, Little Rock, AR 72202 USA
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
RNA-seq; Placenta; Preeclampsia; Co-expression; Gene expression; Microarray; GENE-EXPRESSION; PHYSIOLOGICAL TRANSFORMATION; NETWORK ANALYSIS; SPIRAL ARTERIES; PREECLAMPSIA; MIDGESTATION; FAILURE; PROFILE; GROWTH;
D O I
10.1186/s12864-016-3384-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Mammalian development in utero is absolutely dependent on proper placental development, which is ultimately regulated by the placental genome. The regulation of the placental genome can be directly studied by exploring the underlying organisation of the placental transcriptome through a systematic analysis of gene-wise co-expression relationships. Results: In this study, we performed a comprehensive analysis of human placental co-expression using RNA sequencing and intergrated multiple transcriptome datasets spanning human gestation. We identified modules of co-expressed genes that are preserved across human gestation, and also identifed modules conserved in the mouse indicating conserved molecular networks involved in placental development and gene expression patterns more specific to late gestation. Analysis of co-expressed gene flanking sequences indicated that conserved co-expression modules in the placenta are regulated by a core set of transcription factors, including ZNF423 and EBF1. Additionally, we identified a gene co-expression module enriched for genes implicated in the pregnancy pathology preeclampsia. By using an independnet transcriptome dataset, we show that these co-expressed genes are differentially expressed in preeclampsia. Conclusions: This study represents a comprehensive characterisation of placental co-expression and provides insight into potential transcriptional regulators that govern conserved molecular programs fundamental to placental development.
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页数:13
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