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小鼠中血红素加氧酶-2可变转录本的鉴定与表达

The identification and expression of heme oxygenase-2 alternative transcripts in the mouse.

作者信息

Gibbs L, Willis D, Morgan M J

机构信息

Department of Experimental Pathology, St. Bartholomew's and Royal London School of Medicine and Dentistry, University of London, London EC1M 6BQ, UK.

出版信息

Gene. 1998 Oct 23;221(2):171-7. doi: 10.1016/s0378-1119(98)00477-6.

Abstract

Murine heme oxygenase-2 (HO-2) cDNA sequences were determined through the assembly of mouse expressed sequence tag (EST) sequences using the rat HO-2 sequence as a template. The sequence analysis revealed two mRNA isoforms, probably arising through alternative splicing, which differed in their 5'-untranslated region (UTR), and were named HO-2a and HO-2b. One EST sequence included an extended 3'-UTR and suggested there may be a choice of poly-adenylation (poly-A) signal sequence. Reverse transcriptase polymerase chain reaction (PCR) suggested that HO-2a mRNA may be specifically expressed in the testis, while HO-2b mRNA was present in all tissues analysed. Furthermore, HO-2a and HO-2b transcripts were both found to include the extended 3'-UTR, but these transcripts were detected only in the testis. Northern analysis of a greater range of tissues confirmed the testis-specific expression of HO-2a mRNA and suggested that the transcripts which included the extended 3'-UTR were a small minority of the HO-2 mRNA population. These alternative murine HO-2 transcripts suggest that mechanisms such as mRNA transport, translational efficiency or mRNA turnover may be implicated in the regulation of HO-2 gene expression, most notably in the testis.

摘要

以大鼠血红素加氧酶 -2(HO -2)序列为模板,通过组装小鼠表达序列标签(EST)序列来确定小鼠HO -2 cDNA序列。序列分析揭示了两种mRNA异构体,可能是通过可变剪接产生的,它们在5'-非翻译区(UTR)有所不同,分别命名为HO -2a和HO -2b。一个EST序列包含一个延长的3'-UTR,并提示可能存在多聚腺苷酸化(poly -A)信号序列的选择。逆转录聚合酶链反应(PCR)表明,HO -2a mRNA可能在睾丸中特异性表达,而HO -2b mRNA存在于所有分析的组织中。此外,发现HO -2a和HO -2b转录本均包含延长的3'-UTR,但这些转录本仅在睾丸中检测到。对更多组织的Northern分析证实了HO -2a mRNA在睾丸中的特异性表达,并表明包含延长的3'-UTR的转录本在HO -2 mRNA群体中占少数。这些小鼠HO -2的可变转录本提示,诸如mRNA转运、翻译效率或mRNA周转等机制可能参与了HO -2基因表达的调控,在睾丸中尤为明显。

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