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人类粘蛋白基因MUC2、MUC3、MUC4、MUC5AC、MUC5B和MUC6表达稳定且极大的mRNA,并呈现可变长度多态性。一种分析大型mRNA的改进方法。

Human mucin genes MUC2, MUC3, MUC4, MUC5AC, MUC5B, and MUC6 express stable and extremely large mRNAs and exhibit a variable length polymorphism. An improved method to analyze large mRNAs.

作者信息

Debailleul V, Laine A, Huet G, Mathon P, d'Hooghe M C, Aubert J P, Porchet N

机构信息

Unité INSERM U 377, Laboratoire Gérard Biserte, place de Verdun, 59045 Lille Cedex, France.

出版信息

J Biol Chem. 1998 Jan 9;273(2):881-90. doi: 10.1074/jbc.273.2.881.

Abstract

Of the nine mucin genes that have been characterized, only MUC1 and MUC7 have been fully sequenced, and their transcripts can be detected as distinct bands of predicted size by Northern blot analysis. In contrast, the RNA patterns observed for each of the other MUC genes have usually shown a very high degree of polydispersity. This polydispersity has been believed to be one of the typical features of the mucin mRNAs, but until now, its origin has remained unexplained. In the work described in the present paper, we investigated two possible kinds of explanation for this phenomenon: namely that the extensive polydispersity results from a biological mechanism or that it is artifactual in origin. The data obtained, as a result of improving the purification and blotting methods, allowed us to show that in all of the tissues analyzed, each of the genes, MUC2-6, expresses mRNAs that are stable and are of an unusually large size to be found in eukaryotes (14-24 kilobases). Moreover, allelic variations in length of these mucin transcripts were observed. We demonstrate that these variations are directly related to the variable number of tandem repeat polymorphisms seen at the DNA level.

摘要

在已被鉴定的9个黏蛋白基因中,只有MUC1和MUC7已被完全测序,并且通过Northern印迹分析可将它们的转录本检测为预测大小的清晰条带。相比之下,其他每个MUC基因所观察到的RNA模式通常显示出高度的多分散性。这种多分散性一直被认为是黏蛋白mRNA的典型特征之一,但直到现在,其起源仍未得到解释。在本文所述的研究中,我们探究了对这一现象的两种可能解释:即广泛的多分散性是由生物学机制导致的,或者其起源是人为造成的。由于改进了纯化和印迹方法而获得的数据使我们能够表明,在所有分析的组织中,MUC2 - 6每个基因都表达稳定且在真核生物中异常大(14 - 24千碱基)的mRNA。此外,观察到了这些黏蛋白转录本长度的等位基因变异。我们证明这些变异与在DNA水平上看到的串联重复多态性的可变数量直接相关。

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