A resource for transcriptomic analysis in the mouse brain.

<h4>Background</h4>The transcriptome of the cerebral cortex is remarkably homogeneous, with variations being stronger between individuals than between areas. It is thought that due to the presence of many distinct cell types, differences within one cell population will be averaged with t...

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Autores principales: Charles Plessy, Michela Fagiolini, Akiko Wagatsuma, Norihiro Harasawa, Takenobu Kuji, Atsuko Asaka-Oba, Yukari Kanzaki, Sayaka Fujishima, Kazunori Waki, Hiroyuki Nakahara, Takao K Hensch, Piero Carninci
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Publicado: Public Library of Science (PLoS) 2008
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Acceso en línea:https://doaj.org/article/88f51d81d0d2450e98531e4824c660a6
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spelling oai:doaj.org-article:88f51d81d0d2450e98531e4824c660a62021-11-25T06:11:07ZA resource for transcriptomic analysis in the mouse brain.1932-620310.1371/journal.pone.0003012https://doaj.org/article/88f51d81d0d2450e98531e4824c660a62008-08-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18714383/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>The transcriptome of the cerebral cortex is remarkably homogeneous, with variations being stronger between individuals than between areas. It is thought that due to the presence of many distinct cell types, differences within one cell population will be averaged with the noise from others. Studies of sorted cells expressing the same transgene have shown that cell populations can be distinguished according to their transcriptional profile.<h4>Methodology</h4>We have prepared a low-redundancy set of 16,209 full-length cDNA clones which represents the transcriptome of the mouse visual cortex in its coding and non-coding aspects. Using an independent tag-based approach, CAGE, we confirmed the cortical expression of 72% of the clones. Clones were amplified by PCR and spotted on glass slides, and we interrogated the microarrays with RNA from flow-sorted fluorescent cells from the cerebral cortex of parvalbumin-egfp transgenic mice.<h4>Conclusions</h4>We provide an annotated cDNA clone collection which is particularly suitable for transcriptomic analysis in the mouse brain. Spotting it on microarrays, we compared the transcriptome of EGFP positive and negative cells in a parvalbumin-egfp transgenic background and showed that more than 30% of clones are differentially expressed. Our clone collection will be a useful resource for the study of the transcriptome of single cell types in the cerebral cortex.Charles PlessyMichela FagioliniAkiko WagatsumaNorihiro HarasawaTakenobu KujiAtsuko Asaka-ObaYukari KanzakiSayaka FujishimaKazunori WakiHiroyuki NakaharaTakao K HenschPiero CarninciPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 3, Iss 8, p e3012 (2008)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Charles Plessy
Michela Fagiolini
Akiko Wagatsuma
Norihiro Harasawa
Takenobu Kuji
Atsuko Asaka-Oba
Yukari Kanzaki
Sayaka Fujishima
Kazunori Waki
Hiroyuki Nakahara
Takao K Hensch
Piero Carninci
A resource for transcriptomic analysis in the mouse brain.
description <h4>Background</h4>The transcriptome of the cerebral cortex is remarkably homogeneous, with variations being stronger between individuals than between areas. It is thought that due to the presence of many distinct cell types, differences within one cell population will be averaged with the noise from others. Studies of sorted cells expressing the same transgene have shown that cell populations can be distinguished according to their transcriptional profile.<h4>Methodology</h4>We have prepared a low-redundancy set of 16,209 full-length cDNA clones which represents the transcriptome of the mouse visual cortex in its coding and non-coding aspects. Using an independent tag-based approach, CAGE, we confirmed the cortical expression of 72% of the clones. Clones were amplified by PCR and spotted on glass slides, and we interrogated the microarrays with RNA from flow-sorted fluorescent cells from the cerebral cortex of parvalbumin-egfp transgenic mice.<h4>Conclusions</h4>We provide an annotated cDNA clone collection which is particularly suitable for transcriptomic analysis in the mouse brain. Spotting it on microarrays, we compared the transcriptome of EGFP positive and negative cells in a parvalbumin-egfp transgenic background and showed that more than 30% of clones are differentially expressed. Our clone collection will be a useful resource for the study of the transcriptome of single cell types in the cerebral cortex.
format article
author Charles Plessy
Michela Fagiolini
Akiko Wagatsuma
Norihiro Harasawa
Takenobu Kuji
Atsuko Asaka-Oba
Yukari Kanzaki
Sayaka Fujishima
Kazunori Waki
Hiroyuki Nakahara
Takao K Hensch
Piero Carninci
author_facet Charles Plessy
Michela Fagiolini
Akiko Wagatsuma
Norihiro Harasawa
Takenobu Kuji
Atsuko Asaka-Oba
Yukari Kanzaki
Sayaka Fujishima
Kazunori Waki
Hiroyuki Nakahara
Takao K Hensch
Piero Carninci
author_sort Charles Plessy
title A resource for transcriptomic analysis in the mouse brain.
title_short A resource for transcriptomic analysis in the mouse brain.
title_full A resource for transcriptomic analysis in the mouse brain.
title_fullStr A resource for transcriptomic analysis in the mouse brain.
title_full_unstemmed A resource for transcriptomic analysis in the mouse brain.
title_sort resource for transcriptomic analysis in the mouse brain.
publisher Public Library of Science (PLoS)
publishDate 2008
url https://doaj.org/article/88f51d81d0d2450e98531e4824c660a6
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