RASL11B基因的克隆、基因组组织和组织特异性表达

Katrin Stolle , Michael Schnoor , Georg Fuellen , Michael Spitzer , Paul Cullen , Stefan Lorkowski
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引用次数: 47

摘要

RASL11B是GTPase小蛋白家族的成员,与RAS蛋白高度相似。对RASL11B mRNA的克隆和计算机分析表明,人类RASL11B基因全长约4.5 kb,在染色体4q12位点上有4个外显子。该基因的近端5 '侧区域缺乏TATA盒,但富含gc,包含CCAAT盒和几个Sp1位点。与此一致的是,RASL11B基因在所有被研究的组织中都有表达,在胎盘和原代巨噬细胞中表达水平最高。预测的RASL11B蛋白没有典型的戊酰化信号,表明它可能没有锚定在细胞膜上。TGF-β1作用于THP-1单核细胞成熟为巨噬细胞样细胞和冠状动脉平滑肌细胞时,可诱导RASL11B。这些结果表明RASL11B可能在TGF-β1介导的发育过程和炎症、癌症、动脉硬化等病理生理过程中发挥作用。
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Cloning, genomic organization, and tissue-specific expression of the RASL11B gene

RASL11B is a member of the small GTPase protein family with a high degree of similarity to RAS proteins. Cloning of RASL11B mRNA and in silico analyses revealed that the human RASL11B gene spans about 4.5 kb and comprises four exons on chromosomal locus 4q12. The proximal 5′-flanking region of the gene lacks a TATA box but is GC-rich and contains a CCAAT box and several Sp1 sites. Consistent with this, the RASL11B gene was found to be expressed in all tissues investigated, with highest levels in placenta and in primary macrophages. The predicted RASL11B protein has no typical prenylation signal, indicating that it is probably not anchored to cellular membranes. RASL11B was induced during maturation of THP-1 monocytic cells into macrophage-like cells and in coronary artery smooth muscle cells after treatment with TGF-β1. These results indicate that RASL11B may play a role in TGF-β1-mediated developmental processes and in pathophysiologies such as inflammation, cancer, and arteriosclerosis.

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