Suppr超能文献

来自巴西HAM/TSP患者和无症状HTLV-1携带者分离株的HTLV-1 p12I蛋白序列上的遗传标记。

Genetic markers on the HTLV-1 p12I protein sequences from Brazilian HAM/TSP patients and asymptomatic HTLV-1 carrier isolates.

作者信息

Iñiguez Alena M, Otsuki Koko, Magalhães Gustavo P, Silva Edimilson A, Vicente Ana Carolina P

机构信息

Departamento de Genética, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, 21045-900, Brazil.

出版信息

AIDS Res Hum Retroviruses. 2005 Jun;21(6):580-2. doi: 10.1089/aid.2005.21.580.

Abstract

The human T cell leukemia/lymphotropic virus type-1 (HTLV-1) genome has approximately 9 kb and contains the pX region that codes for regulatory and accessory proteins. The pX ORF-I encodes for the p12 protein, a 99 aa peptide, which presents several functional putative domains, such as leucine zipper motifs, SH3- binding motifs, and a dileucine motif, p12I. Also, a rare p12IK88 allele was found mainly in HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) patients, suggesting it is a marker of pathogenesis, although recent studies showed p12IK in asymptomatic HTLV-1 carriers. To extend the observations on p12I motifs, we sequenced 26 p12I from HAM/TSP patients and asymptomatic HTLV-1 carriers. Amino acid analysis of 48 p12I motifs demonstrated the presence of several alleles, but the allelic variation, including p12IK, was not prevalent in HAM/TSP isolates. Nonetheless, some genetic markers were recognized in association with isolates from HTLV-1a subgroup B and Brazilian HTLV-1aA strains.

摘要

人类1型嗜T细胞白血病/淋巴瘤病毒(HTLV-1)基因组约有9 kb,包含编码调节蛋白和辅助蛋白的pX区域。pX开放阅读框I编码p12蛋白,这是一种99个氨基酸的肽,具有几个功能性推定结构域,如亮氨酸拉链基序、SH3结合基序和双亮氨酸基序p12I。此外,一种罕见的p12IK88等位基因主要在HTLV-1相关脊髓病/热带痉挛性截瘫(HAM/TSP)患者中发现,提示它是发病机制的一个标志物,尽管最近的研究显示无症状HTLV-1携带者中也存在p12IK。为了扩展对p12I基序的观察,我们对26个来自HAM/TSP患者和无症状HTLV-1携带者的p12I进行了测序。对48个p12I基序的氨基酸分析表明存在几个等位基因,但包括p12IK在内的等位基因变异在HAM/TSP分离株中并不普遍。尽管如此,一些遗传标志物与HTLV-1a亚组B和巴西HTLV-1aA株的分离株相关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验