BRCA1 Cis调控元件特征的集成芯片评价

Apeksha Arun Bhandarkar, Smeeta Shrestha
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引用次数: 0

摘要

基因组顺式调控元件支持基因转录景观,在发育过程中通过与不同转录因子和共调节剂的相互作用微调基因的时空表达。这些调控元件保守性差,异质性高,对其在基因表达中的作用了解有限。在这里,我们使用一个众所周知的人类肿瘤抑制基因,乳腺癌1型(BRCA1)和UCSC人类基因组浏览器数据库报道了计算机推定的顺式调控增强子元件及其特征。我们报道了一个2kb的双精英增强子GH17J043079,位于BRCA1基因的内含子12中。该增强子与NBR1、NBR2、TMEM106A、RPL27和VAT1基因启动子相互作用。GH17J043079在人胚胎干细胞、癌细胞、肝细胞特异性转录因子中显示组蛋白活性,并富含Alu元素,表明具有潜在的基因重排能力。此外,在不同人群中,rs4793197、rs8176190、rs8176192、rs8176193和rs8176194等位基因频率存在差异。我们对BRCA1中GH17J043079元件中存在的特征进行了计算机回顾,有助于假设复杂的转录调控。这种基于候选基因的顺式调控元件特征分析有助于阐明复杂的基因组结构、基因调控及其对复杂疾病的影响。
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Integrative In-Silico Evaluation of Features on BRCA1 Cis Regulatory Element
Genomic cis regulatory elements support the gene transcriptional landscape which fine tune spatiotemporal gene expression via interaction with different transcription factors and co modulators during development. These regulatory elements are poorly conserved, highly heterogenous with limited understanding of their role in gene expression. Here we use a well-known human tumor suppressor gene, Breast Cancer Type 1 ( BRCA1 ) and UCSC human genome browser database to report the in-silico putative cis regulatory enhancer element and its features. We report a 2kb double elite enhancer, GH17J043079 located within intron 12 of the BRCA1 gene. The enhancer interacts with NBR1 , NBR2 , TMEM106A and RPL27 and VAT1 gene promoters. GH17J043079 showed histone activity in human embryonic stem cells, cancerous cells, housed transcription factors specific to liver cells and was enriched with Alu elements, indicative of ability for potential gene rearrangements. Additionally, it contained eQTLs, rs4793197, rs8176190, rs8176192, rs8176193 and rs8176194 with disparity in allele frequency across populations. Our in-silico review on the features present within GH17J043079 element in BRCA1 helps to postulate an intricate transcription regulation. Such candidate based analysis of features within cis regulatory element on a gene can help elucidate intricate genomic architecture, gene regulation and its impact on complex disorders.
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