Welham Simon J M, Clark Adrian J L, Salter Andrew M
University of Nottingham, Division of Nutritional Sciences, Sutton Bonington Campus, Loughborough, Leicestershire, LE12 5RD, UK.
BMC Mol Biol. 2009 Apr 8;10:30. doi: 10.1186/1471-2199-10-30.
The leukocyte common antigen related receptor (LAR) protein has been shown to modulate the signal transduction of a number of different growth factors, including insulin and insulin-like growth factor 1. Splice variants exhibit differing roles and are expressed according to tissue type and developmental stage.
Using 5'RACE, we identified a 5'UTR within intron 11 of the rat LAR gene. We demonstrated that this gives rise to a novel isoform of the LAR transcript encoded from the identified region within intron 11. By priming across the site from exon 11 to exon 15 we show that the novel 5'UTR is not represented in the full-length transcript and thus, it produces a truncated form of the LAR mRNA. We examined the tissue distribution of this novel isoform and found it to be exclusively expressed in liver. We additionally identified a liver specific 150 kDa band with western blotting which we propose may represent the protein product of the novel transcript. Luciferase assays showed the region immediately upstream of the 5'UTR to possesses considerable promoter activity and that this may be conferred by the presence of a number of putative binding sites for liver enriched transcription factors.
In summary, we describe a novel, liver specific, truncated isoform of the LAR transcript transcribed under the control of an intronic promoter, potentially representing a previously unidentified modulator of hepatic insulin signalling.
白细胞共同抗原相关受体(LAR)蛋白已被证明可调节多种不同生长因子的信号转导,包括胰岛素和胰岛素样生长因子1。剪接变体表现出不同的作用,并根据组织类型和发育阶段表达。
使用5'RACE,我们在大鼠LAR基因的第11内含子中鉴定出一个5'UTR。我们证明这会产生一种从第11内含子内的鉴定区域编码的LAR转录本的新型异构体。通过从外显子11到外显子15跨越该位点进行引物延伸,我们表明全长转录本中不存在这种新型5'UTR,因此,它产生了一种截短形式的LAR mRNA。我们检查了这种新型异构体的组织分布,发现它仅在肝脏中表达。我们还通过蛋白质印迹法鉴定出一条肝脏特异性的150 kDa条带,我们认为它可能代表新型转录本的蛋白质产物。荧光素酶测定表明,5'UTR紧邻上游区域具有相当大的启动子活性,这可能是由许多肝脏富集转录因子的假定结合位点的存在所赋予的。
总之,我们描述了一种新型的、肝脏特异性的、在一个内含子启动子控制下转录的LAR转录本截短异构体,它可能代表一种以前未被识别的肝脏胰岛素信号调节剂。