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人血清淀粉样蛋白A的异质性。通过cDNA序列分析显示来自同一个体的五种不同变体。

Heterogeneity of human serum amyloid A protein. Five different variants from one individual demonstrated by cDNA sequence analysis.

作者信息

Steinkasserer A, Weiss E H, Schwaeble W, Linke R P

机构信息

Institut für Immunologie, Universität München, Federal Republic of Germany.

出版信息

Biochem J. 1990 May 15;268(1):187-93. doi: 10.1042/bj2680187.

Abstract

Serum amyloid A (SAA), a chemically polymorphic protein, is the most sensitive marker protein of the acute phase and the precursor of reactive amyloidosis, which is characterized by deposits of amyloid A protein (AA). We investigated the variability of the SAA gene family in one individual by sequencing 11 SAA-specific clones from an acute-phase-liver cDNA library. At least five different SAA variants were deduced from six different cDNAs. The 3' untranslated gene segments fall into two groups, based on nucleotide sequence and variability in length. Various nucleotide and amino acid substitutions were found predominantly in the 3' portion. Some of these substitutions are unique and increase the number of SAA variants in one individual to at least five. Moreover, genomic DNA of four individuals was examined by analysis of restriction-fragment length polymorphism. Besides two conserved strongly labelled bands, additional polymorphic bands were observed, indicating isotypic and/or allotypic SAA variations. Finally, three different mRNA species were detected by Northern-blot analysis, a finding that might be of relevance for the stability of SAA transcripts.

摘要

血清淀粉样蛋白A(SAA)是一种化学多态性蛋白,是急性期最敏感的标志物蛋白,也是反应性淀粉样变性的前体,其特征是淀粉样蛋白A(AA)沉积。我们通过对急性期肝脏cDNA文库中的11个SAA特异性克隆进行测序,研究了一个个体中SAA基因家族的变异性。从6个不同的cDNA中推断出至少5种不同的SAA变体。基于核苷酸序列和长度变异性,3'非翻译基因片段分为两组。各种核苷酸和氨基酸取代主要出现在3'部分。其中一些取代是独特的,使一个个体中的SAA变体数量增加到至少5种。此外,通过分析限制性片段长度多态性对4个人的基因组DNA进行了检测。除了两条保守的强条带外,还观察到额外的多态性条带,表明存在同型和/或异型SAA变异。最后,通过Northern印迹分析检测到三种不同的mRNA种类,这一发现可能与SAA转录本的稳定性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0aa/1131410/74f9146cdf50/biochemj00183-0186-a.jpg

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