Xia Chang, He Rong, Ruan Qiang, Guo Jin-jin, Liu Qing, Ji Yao-hua, Wei Hong-bing, Chen Shu-rong, Liu Lan-qing
The Virology Laboratory of The National Key Laboratory, Ministry of Health for Congenital Malformation Research. The Second Affiliated Hospital of China Medical University, Shenyang 110004, China.
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2006 Mar;20(1):23-5.
To study the polymorphism of human cytomegalovirus US28 gene in children and investigate the relationship between the polymorphism and pathogenesis.
The FQ-PCR was carried out to determine the DNA quantity of clinical isolate and then the segmental PCR and HMA-SSCP were performed to test the mutation of US28 gene. The typical isolates from different diseases were selected to clone and sequence, then the results were analyzed.
The nucleic acid mutation is frequent among the sequence of US28, those mutations focus on the two ends of US28, but most of them are sense mutation. The important functional groups of US28 are highly conserved. The amino acid mutation of some isolates resulted in the change of secondary structure, but the phylogenetic tree analysis did not show any clear association between the pathogenesis and the distribution of clinical isolates. The comparison of US28 sequences from AIDS patients with the sequences from children in our study showed that both sequences have their own specific high mutation points.
There is polymorphism among the HCMV-US28 gene of clinical isolates from children. There observed no clear relationship was between the pathogenesis and the distribution of clinical isolates.
研究儿童人巨细胞病毒US28基因的多态性,并探讨该多态性与发病机制之间的关系。
采用荧光定量聚合酶链反应(FQ-PCR)检测临床分离株的DNA量,然后进行分段聚合酶链反应(PCR)和异源双链构象多态性分析(HMA-SSCP)检测US28基因的突变情况。选取不同疾病的典型分离株进行克隆测序,并对结果进行分析。
US28基因序列中核酸突变较为频繁,这些突变集中在US28的两端,但大多为同义突变。US28的重要功能基团高度保守。部分分离株的氨基酸突变导致二级结构改变,但系统发育树分析未显示发病机制与临床分离株分布之间存在明显关联。艾滋病患者的US28序列与本研究中儿童的序列比较显示,两者序列均有各自特定的高突变位点。
儿童临床分离株的人巨细胞病毒-US28基因存在多态性。未观察到发病机制与临床分离株分布之间存在明显关系。