Expressional artifact caused by a co-injection marker rol-6 in C. elegans.

In transgenic research, selection markers have greatly facilitated the generation of transgenic animals. A prerequisite for a suitable selection marker to be used along with a test gene of interest is that the marker should not affect the phenotype of interest in transformed animals. One of the most...

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Main Authors: HoYong Jin, Scott W Emmons, Byunghyuk Kim
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0224533
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spelling doaj-3330a6e400ff459291fd1c816f2c6b152021-03-04T11:20:46ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-011412e022453310.1371/journal.pone.0224533Expressional artifact caused by a co-injection marker rol-6 in C. elegans.HoYong JinScott W EmmonsByunghyuk KimIn transgenic research, selection markers have greatly facilitated the generation of transgenic animals. A prerequisite for a suitable selection marker to be used along with a test gene of interest is that the marker should not affect the phenotype of interest in transformed animals. One of the most common selection markers used in C. elegans transgenic approaches is the rol-6 co-injection marker, which induces a behavioral roller phenotype due to a cuticle defect but is not known to have other side effects. However, we found that the rol-6 co-injection marker can cause expression of GFP in the test sequence in a male-specific interneuron called CP09. We found that the rol-6 gene sequence included in the marker plasmid is responsible for this unwanted expression. Accordingly, the use of the rol-6 co-injection marker is not recommended when researchers intend to examine precise expression or perform functional studies especially targeting male C. elegans neurons. The rol-6 sequence region we identified can be used to drive a specific expression in CP09 neuron for future research.https://doi.org/10.1371/journal.pone.0224533
collection DOAJ
language English
format Article
sources DOAJ
author HoYong Jin
Scott W Emmons
Byunghyuk Kim
spellingShingle HoYong Jin
Scott W Emmons
Byunghyuk Kim
Expressional artifact caused by a co-injection marker rol-6 in C. elegans.
PLoS ONE
author_facet HoYong Jin
Scott W Emmons
Byunghyuk Kim
author_sort HoYong Jin
title Expressional artifact caused by a co-injection marker rol-6 in C. elegans.
title_short Expressional artifact caused by a co-injection marker rol-6 in C. elegans.
title_full Expressional artifact caused by a co-injection marker rol-6 in C. elegans.
title_fullStr Expressional artifact caused by a co-injection marker rol-6 in C. elegans.
title_full_unstemmed Expressional artifact caused by a co-injection marker rol-6 in C. elegans.
title_sort expressional artifact caused by a co-injection marker rol-6 in c. elegans.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description In transgenic research, selection markers have greatly facilitated the generation of transgenic animals. A prerequisite for a suitable selection marker to be used along with a test gene of interest is that the marker should not affect the phenotype of interest in transformed animals. One of the most common selection markers used in C. elegans transgenic approaches is the rol-6 co-injection marker, which induces a behavioral roller phenotype due to a cuticle defect but is not known to have other side effects. However, we found that the rol-6 co-injection marker can cause expression of GFP in the test sequence in a male-specific interneuron called CP09. We found that the rol-6 gene sequence included in the marker plasmid is responsible for this unwanted expression. Accordingly, the use of the rol-6 co-injection marker is not recommended when researchers intend to examine precise expression or perform functional studies especially targeting male C. elegans neurons. The rol-6 sequence region we identified can be used to drive a specific expression in CP09 neuron for future research.
url https://doi.org/10.1371/journal.pone.0224533
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