Site-directed mutagenesis of long QT syndrome KCNQ1 gene

LI Wei1, WANG Bin1, XU Qiumei1, KE Qinmei1, YANG Junguo2, DU Rong2, TIAN Li2, WANG Qing3

Front. Med. ›› 2008, Vol. 2 ›› Issue (1) : 100-104.

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Front. Med. ›› 2008, Vol. 2 ›› Issue (1) : 100-104. DOI: 10.1007/s11684-008-0018-x

Site-directed mutagenesis of long QT syndrome KCNQ1 gene

  • LI Wei1, WANG Bin1, XU Qiumei1, KE Qinmei1, YANG Junguo2, DU Rong2, TIAN Li2, WANG Qing3
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Abstract

To construct a polymerase chain reaction (PCR) site-directed mutagenesis of the long QT syndrome KCNQ1 gene in vitro, two sets of primers were designed according to the sequence of KCNQ1 cDNA and a mismatch was introduced into primers. Mutagenesis was performed in a two-step PCR. The amplified fragments from the third PCR which contained the mutation site were sub-cloned into the T-vector pCR2.1. Then, the fragments containing the mutation site was obtained from pCR2.1 using restriction enzymes digestion and inserted into the same restriction site of pIRES2-EGFP-KCNQ1. The sequencing analysis shows that the mutation site was correct. Mutation from A to G in site 983 of KCNQ1 cDNA was found. Using the Effectene transfection reagent, pIRES2-EGFP-KCNQ1 (G983A) was transfected into HEK cells successfully. These results may shed light on further functional study of KCNQ1 gene.

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LI Wei, WANG Bin, XU Qiumei, KE Qinmei, YANG Junguo, DU Rong, TIAN Li, WANG Qing. Site-directed mutagenesis of long QT syndrome KCNQ1 gene. Front. Med., 2008, 2(1): 100‒104 https://doi.org/10.1007/s11684-008-0018-x

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