Cargando…

Minimal Purkinje Cell-Specific PCP2/L7 Promoter Virally Available for Rodents and Non-human Primates

Cell-type-specific promoters in combination with viral vectors and gene-editing technology permit efficient gene manipulation in specific cell populations. Cerebellar Purkinje cells play a pivotal role in cerebellar functions. Although the Purkinje cell-specific L7 promoter is widely used for the ge...

Descripción completa

Detalles Bibliográficos
Autores principales: Nitta, Keisuke, Matsuzaki, Yasunori, Konno, Ayumu, Hirai, Hirokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552061/
https://www.ncbi.nlm.nih.gov/pubmed/28828391
http://dx.doi.org/10.1016/j.omtm.2017.07.006
_version_ 1783256402120146944
author Nitta, Keisuke
Matsuzaki, Yasunori
Konno, Ayumu
Hirai, Hirokazu
author_facet Nitta, Keisuke
Matsuzaki, Yasunori
Konno, Ayumu
Hirai, Hirokazu
author_sort Nitta, Keisuke
collection PubMed
description Cell-type-specific promoters in combination with viral vectors and gene-editing technology permit efficient gene manipulation in specific cell populations. Cerebellar Purkinje cells play a pivotal role in cerebellar functions. Although the Purkinje cell-specific L7 promoter is widely used for the generation of transgenic mice, it remains unsuitable for viral vectors because of its large size (3 kb) and exceedingly weak promoter activity. Here, we found that the 0.8-kb region (named here as L7-6) upstream of the transcription initiation codon in the first exon was alone sufficient as a Purkinje cell-specific promoter, presenting a far stronger promoter activity over the original 3-kb L7 promoter with a sustained significant specificity to Purkinje cells. Intravenous injection of adeno-associated virus vectors that are highly permeable to the blood-brain barrier confirmed the Purkinje cell specificity of the L7-6 in the CNS. The features of the L7-6 were also preserved in the marmoset, a non-human primate. The high sequence homology of the L7-6 among mouse, marmoset, and human suggests the preservation of the promoter strength and Purkinje cell specificity features also in humans. These findings suggest that L7-6 will facilitate the cerebellar research targeting the pathophysiology and gene therapy of cerebellar disorders.
format Online
Article
Text
id pubmed-5552061
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher American Society of Gene & Cell Therapy
record_format MEDLINE/PubMed
spelling pubmed-55520612017-08-21 Minimal Purkinje Cell-Specific PCP2/L7 Promoter Virally Available for Rodents and Non-human Primates Nitta, Keisuke Matsuzaki, Yasunori Konno, Ayumu Hirai, Hirokazu Mol Ther Methods Clin Dev Original Article Cell-type-specific promoters in combination with viral vectors and gene-editing technology permit efficient gene manipulation in specific cell populations. Cerebellar Purkinje cells play a pivotal role in cerebellar functions. Although the Purkinje cell-specific L7 promoter is widely used for the generation of transgenic mice, it remains unsuitable for viral vectors because of its large size (3 kb) and exceedingly weak promoter activity. Here, we found that the 0.8-kb region (named here as L7-6) upstream of the transcription initiation codon in the first exon was alone sufficient as a Purkinje cell-specific promoter, presenting a far stronger promoter activity over the original 3-kb L7 promoter with a sustained significant specificity to Purkinje cells. Intravenous injection of adeno-associated virus vectors that are highly permeable to the blood-brain barrier confirmed the Purkinje cell specificity of the L7-6 in the CNS. The features of the L7-6 were also preserved in the marmoset, a non-human primate. The high sequence homology of the L7-6 among mouse, marmoset, and human suggests the preservation of the promoter strength and Purkinje cell specificity features also in humans. These findings suggest that L7-6 will facilitate the cerebellar research targeting the pathophysiology and gene therapy of cerebellar disorders. American Society of Gene & Cell Therapy 2017-07-27 /pmc/articles/PMC5552061/ /pubmed/28828391 http://dx.doi.org/10.1016/j.omtm.2017.07.006 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Nitta, Keisuke
Matsuzaki, Yasunori
Konno, Ayumu
Hirai, Hirokazu
Minimal Purkinje Cell-Specific PCP2/L7 Promoter Virally Available for Rodents and Non-human Primates
title Minimal Purkinje Cell-Specific PCP2/L7 Promoter Virally Available for Rodents and Non-human Primates
title_full Minimal Purkinje Cell-Specific PCP2/L7 Promoter Virally Available for Rodents and Non-human Primates
title_fullStr Minimal Purkinje Cell-Specific PCP2/L7 Promoter Virally Available for Rodents and Non-human Primates
title_full_unstemmed Minimal Purkinje Cell-Specific PCP2/L7 Promoter Virally Available for Rodents and Non-human Primates
title_short Minimal Purkinje Cell-Specific PCP2/L7 Promoter Virally Available for Rodents and Non-human Primates
title_sort minimal purkinje cell-specific pcp2/l7 promoter virally available for rodents and non-human primates
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552061/
https://www.ncbi.nlm.nih.gov/pubmed/28828391
http://dx.doi.org/10.1016/j.omtm.2017.07.006
work_keys_str_mv AT nittakeisuke minimalpurkinjecellspecificpcp2l7promotervirallyavailableforrodentsandnonhumanprimates
AT matsuzakiyasunori minimalpurkinjecellspecificpcp2l7promotervirallyavailableforrodentsandnonhumanprimates
AT konnoayumu minimalpurkinjecellspecificpcp2l7promotervirallyavailableforrodentsandnonhumanprimates
AT hiraihirokazu minimalpurkinjecellspecificpcp2l7promotervirallyavailableforrodentsandnonhumanprimates