Suppr超能文献

[伴有原发性深静脉瓣膜功能不全的大隐静脉曲张相关基因的筛选与克隆]

[Screening and cloning of genes related to varicose great saphenous vein accompanying with primary deep vein valve insufficiency].

作者信息

Wang Shenming, Yin Henghui, Wang Jinsong, Hu Zuojun, Huang Xueling

机构信息

Department of Vascular Surgery, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.

出版信息

Zhonghua Wai Ke Za Zhi. 2002 Dec;40(12):909-11.

Abstract

OBJECTIVE

To screen the genes related to the occurrence and development of varicosis of the great saphenous vein in the patients with primary deep vein valve insufficiency.

METHODS

Using mRNA fluorescent differential display reverse transcriptive polymerase chain reaction (FDD-RTPCR), different genes expressed in the varicose great saphenous veins in patients with primary deep vein valve insufficiency and corresponding normal human tissues were compared. Differentially expressed cDNA fragments confirmed by Northern blot were compared and then cloned into the pGEM-Teasy vector. Positive clones were selected and sequenced. All the sequences were put into GenBank and analyzed by BLASTN software to search for their genetic origins.

RESULTS

Altogether 37 different cDNA fragments were obtained and 30 of which were confirmed by Northern blot. Analysis of the sequences by BLASTN software showed that C(610) fragment (NO. 18 cDNA clone) shared 96% homology with the mRNA sequence of the human Mckusick-Kaufman syndrome gene (MKKS gene).

CONCLUSION

C(610) fragment is highly homologous with the mRNA sequence of the human MKKS gene and is closely related to the development of varicosis of the great saphenous vein in patients with primary deep vein valve insufficiency.

摘要

目的

筛选原发性深静脉瓣膜功能不全患者大隐静脉曲张发生发展相关基因。

方法

采用mRNA荧光差异显示逆转录聚合酶链反应(FDD-RTPCR),比较原发性深静脉瓣膜功能不全患者曲张大隐静脉及相应正常人体组织中表达的不同基因。对经Northern印迹证实的差异表达cDNA片段进行比较,然后克隆到pGEM-Teasy载体中。筛选阳性克隆并测序。将所有序列提交到GenBank,并用BLASTN软件进行分析以寻找其基因来源。

结果

共获得37个不同的cDNA片段,其中30个经Northern印迹证实。用BLASTN软件对序列进行分析显示,C(610)片段(第18号cDNA克隆)与人麦库西克-考夫曼综合征基因(MKKS基因)的mRNA序列具有96%的同源性。

结论

C(610)片段与人MKKS基因的mRNA序列高度同源,与原发性深静脉瓣膜功能不全患者大隐静脉曲张的发生密切相关。

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