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转钴胺素II信使核糖核酸在人体组织以及来自正常和转钴胺素II缺乏患者的培养成纤维细胞中的表达。

Expression of transcobalamin II mRNA in human tissues and cultured fibroblasts from normal and transcobalamin II-deficient patients.

作者信息

Li N, Seetharam S, Rosenblatt D S, Seetharam B

机构信息

Department of Biochemistry, Medical College of Wisconsin, Milwaukee 53226.

出版信息

Biochem J. 1994 Jul 15;301 ( Pt 2)(Pt 2):585-90. doi: 10.1042/bj3010585.

Abstract

Transcobalamin II (TCII) is an important plasma transporter of cobalamin (Cbl; vitamin B12). In the present study, TCII gene expression in human and rat tissues and in the fibroblasts of patients with TCII deficiency was investigated. Northern-blot analyses revealed expression of TCII mRNA in many human and rat tissues. In humans, this was 14-fold higher in the kidney than in liver, whereas in the rat the levels of expression were similar in the kidney and liver. Southern-blot analysis of genomic DNA from several species revealed sequence similarity in TCII across species. Metabolic labelling and ribonuclease protection assay revealed a 43 kDa TCII protein and a fully protected TCII mRNA band in normal fibroblasts but not in fibroblasts from three TCII-deficient patients. Southern-blot analysis of genomic DNA from all these fibroblasts revealed identical restriction patterns on BamHI, HindIII, KpnI, MspI and EcoRI digestion. On the basis of these results, we suggest that TCII is expressed in multiple tissues, and its level of expression in tissues varies within the same and across species. Furthermore, the TCII deficiency characterized in this study is due to the absence of TCII protein which in turn is due to the absence or extremely low levels of its mRNA and not to detectable gross alterations in the gene structure.

摘要

转钴胺素II(TCII)是钴胺素(Cbl;维生素B12)的一种重要血浆转运蛋白。在本研究中,对人和大鼠组织以及TCII缺乏症患者的成纤维细胞中的TCII基因表达进行了研究。Northern印迹分析显示,TCII mRNA在许多人和大鼠组织中均有表达。在人类中,肾脏中的表达比肝脏高14倍,而在大鼠中,肾脏和肝脏中的表达水平相似。对几种物种的基因组DNA进行Southern印迹分析,结果显示不同物种间的TCII存在序列相似性。代谢标记和核糖核酸酶保护试验显示,正常成纤维细胞中有一条43 kDa的TCII蛋白条带和一条完全受保护的TCII mRNA条带,而三名TCII缺乏症患者的成纤维细胞中则没有。对所有这些成纤维细胞的基因组DNA进行Southern印迹分析,结果显示,用BamHI、HindIII、KpnI、MspI和EcoRI消化后的限制性图谱相同。基于这些结果,我们认为TCII在多种组织中表达,其在组织中的表达水平在同一物种内和不同物种间存在差异。此外,本研究中所表征的TCII缺乏症是由于缺乏TCII蛋白,而这又是由于其mRNA缺失或水平极低,而非基因结构中可检测到的明显改变所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e8/1137121/42f608cc9185/biochemj00083-0267-a.jpg

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