Literature DB >> 20041603

[Construction of GJB2 mutations common in Chinese EGFP fusion protein vectors].

Yanping Zhang1, Yuanding Zhang, Lina Li, Lei Ma, Yurui Sun, Zonglin Zhang, Jinwei Liu, Huiyan Deng, Wei Zhu.   

Abstract

OBJECTIVE: To construct GJB2 gene mutations common in Chinese EGFP fusion protein vectors, and to search for better way to study the mechanism of deletion mutations in GJB2 gene.
METHOD: Non-fusion protein vectors of 235delC, 299-300 del AT and 176 del 16 bp were first made by point mutation methods in vitro. Then expression part of the upper 3 mutations were amplified by PCR and the PCR products were cloned into TA cloning vector. After cutting by restriction enzymes EcoRI/BamHI, three deletion mutations were inserted into pEGFP-N1 vector. Sequencing was used to verify the validity of the fusion protein vectors. HEK293 cells were transfected with the recombinant DNA samples by the liposome complex method. RESULT: The recombined plasmids were highly expressed in HEK293 cells. Green fluorescence signals were distributed uniformly in cytoplasm.
CONCLUSION: GJB2 mutations common in Chinese EGFP fusion protein vectors were constructed successfully. It may provide a better way to explore the reasons of nonsyndromic hearing loss common in Chinese.

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Year:  2009        PMID: 20041603

Source DB:  PubMed          Journal:  Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi        ISSN: 1001-1781


  1 in total

1.  A screening analysis of the GJB2 c.176 del 16 mutation responsible for hereditary deafness in a Chinese family.

Authors:  Hao Jiang; Xi Shi; Shiwei Qiu; Yanfen Dong; Yuehua Qiao; Dongzhi Wei
Journal:  J Otol       Date:  2016-09-12
  1 in total

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