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p110δ磷脂酰肌醇-3激酶基因表达的调控

Regulation of p110delta PI 3-kinase gene expression.

作者信息

Kok Klaartje, Nock Gemma E, Verrall Elizabeth A G, Mitchell Michael P, Hommes Daan W, Peppelenbosch Maikel P, Vanhaesebroeck Bart

机构信息

Centre for Cell Signalling, Institute of Cancer, Queen Mary University of London, Charterhouse Square, London, United Kingdom.

出版信息

PLoS One. 2009;4(4):e5145. doi: 10.1371/journal.pone.0005145. Epub 2009 Apr 9.

Abstract

BACKGROUND

Despite an intense interest in the biological functions of the phosphoinositide 3-kinase (PI3K) signalling enzymes, little is known about the regulation of PI3K gene expression. This also applies to the leukocyte-enriched p110delta catalytic subunit of PI3K, an enzyme that has attracted widespread interest because of its role in immunity and allergy.

PRINCIPAL FINDINGS

We show that p110delta expression is mainly regulated at the transcriptional level. In fibroblasts, lymphocytes and myeloid cells, p110delta gene transcription appears to be constitutive and not subject to acute stimulation. 5'RACE experiments revealed that p110delta mRNA transcripts contain distinct upstream untranslated exons (named exon -1, -2a, -2b, -2c and -2d), which are located up to 81 kb upstream of the translational start codon in exon 1. The levels of all the different p110delta transcripts are higher in leukocytes compared to non-leukocytes, with the p110delta transcript containing exon -2a most abundantly expressed. We have identified a highly conserved transcription factor (TF) binding cluster in the p110delta gene which has enhanced promoter activity in leukocytes compared to non-leukocytes. In human, this TF cluster is located immediately upstream of exon -2a whilst in mouse, it is located within exon -2a.

CONCLUSION

This study identifies a conserved PIK3CD promoter region that may account for the predominant leukocyte expression of p110delta.

摘要

背景

尽管人们对磷酸肌醇3激酶(PI3K)信号酶的生物学功能有着浓厚兴趣,但对PI3K基因表达的调控却知之甚少。这同样适用于PI3K中富含白细胞的p110δ催化亚基,该酶因其在免疫和过敏中的作用而引起了广泛关注。

主要发现

我们发现p110δ的表达主要在转录水平受到调控。在成纤维细胞、淋巴细胞和髓细胞中,p110δ基因转录似乎是组成性的,不受急性刺激的影响。5'RACE实验表明,p110δmRNA转录本包含不同的上游非翻译外显子(命名为外显子-1、-2a、-2b、-2c和-2d),它们位于外显子1中翻译起始密码子上游达81 kb处。与非白细胞相比,所有不同的p110δ转录本在白细胞中的水平更高,其中包含外显子-2a的p110δ转录本表达最为丰富。我们在p110δ基因中鉴定出一个高度保守的转录因子(TF)结合簇,与非白细胞相比,该簇在白细胞中具有增强的启动子活性。在人类中,这个TF簇位于外显子-2a的紧邻上游,而在小鼠中,它位于外显子-2a内。

结论

本研究鉴定出一个保守的PIK3CD启动子区域,该区域可能解释了p110δ在白细胞中的主要表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cb0/2663053/55cb680a90cd/pone.0005145.g001.jpg

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