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HEK293T Cells Are Heterozygous for CCR5 Delta 32 Mutation

C-C chemokine receptor 5 (CCR5) is a receptor for chemokines and a co-receptor for HIV-1 entry into the target CD4+ cells. CCR5 delta 32 deletion is a loss-of-function mutation, resistant to HIV-1 infection. We tried to induce the CCR5 delta 32 mutation harnessing the genome editing technique, CRISP...

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Detalles Bibliográficos
Autores principales: Qi, Chunxia, Jia, Xiaopeng, Lu, Lingling, Ma, Ping, Wei, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820142/
https://www.ncbi.nlm.nih.gov/pubmed/27042825
http://dx.doi.org/10.1371/journal.pone.0152975
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author Qi, Chunxia
Jia, Xiaopeng
Lu, Lingling
Ma, Ping
Wei, Min
author_facet Qi, Chunxia
Jia, Xiaopeng
Lu, Lingling
Ma, Ping
Wei, Min
author_sort Qi, Chunxia
collection PubMed
description C-C chemokine receptor 5 (CCR5) is a receptor for chemokines and a co-receptor for HIV-1 entry into the target CD4+ cells. CCR5 delta 32 deletion is a loss-of-function mutation, resistant to HIV-1 infection. We tried to induce the CCR5 delta 32 mutation harnessing the genome editing technique, CRISPR-Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats, CRISPR and CRISPR associated protein 9, Cas9) in the commonly used cell line human embryonic kidney HEK 293T cells. Surprisingly, we found that HEK293T cells are heterozygous for CCR5 delta 32 mutation, in contrast to the wild type CCR5 cells, human acute T cell leukemia cell line Jurkat and human breast adenocarcinoma cell line MDA-MB-231 cells. This finding indicates that at least one human cell line is heterozygous for the CCR5 delta 32 mutation. We also found that in PCR amplification, wild type CCR5 DNA and mutant delta 32 DNA can form mismatched heteroduplex and move slowly in gel electrophoresis.
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spelling pubmed-48201422016-04-22 HEK293T Cells Are Heterozygous for CCR5 Delta 32 Mutation Qi, Chunxia Jia, Xiaopeng Lu, Lingling Ma, Ping Wei, Min PLoS One Research Article C-C chemokine receptor 5 (CCR5) is a receptor for chemokines and a co-receptor for HIV-1 entry into the target CD4+ cells. CCR5 delta 32 deletion is a loss-of-function mutation, resistant to HIV-1 infection. We tried to induce the CCR5 delta 32 mutation harnessing the genome editing technique, CRISPR-Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats, CRISPR and CRISPR associated protein 9, Cas9) in the commonly used cell line human embryonic kidney HEK 293T cells. Surprisingly, we found that HEK293T cells are heterozygous for CCR5 delta 32 mutation, in contrast to the wild type CCR5 cells, human acute T cell leukemia cell line Jurkat and human breast adenocarcinoma cell line MDA-MB-231 cells. This finding indicates that at least one human cell line is heterozygous for the CCR5 delta 32 mutation. We also found that in PCR amplification, wild type CCR5 DNA and mutant delta 32 DNA can form mismatched heteroduplex and move slowly in gel electrophoresis. Public Library of Science 2016-04-04 /pmc/articles/PMC4820142/ /pubmed/27042825 http://dx.doi.org/10.1371/journal.pone.0152975 Text en © 2016 Qi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Qi, Chunxia
Jia, Xiaopeng
Lu, Lingling
Ma, Ping
Wei, Min
HEK293T Cells Are Heterozygous for CCR5 Delta 32 Mutation
title HEK293T Cells Are Heterozygous for CCR5 Delta 32 Mutation
title_full HEK293T Cells Are Heterozygous for CCR5 Delta 32 Mutation
title_fullStr HEK293T Cells Are Heterozygous for CCR5 Delta 32 Mutation
title_full_unstemmed HEK293T Cells Are Heterozygous for CCR5 Delta 32 Mutation
title_short HEK293T Cells Are Heterozygous for CCR5 Delta 32 Mutation
title_sort hek293t cells are heterozygous for ccr5 delta 32 mutation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820142/
https://www.ncbi.nlm.nih.gov/pubmed/27042825
http://dx.doi.org/10.1371/journal.pone.0152975
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