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1Identification of genes differentially expressed in the embryonic pig cerebral cortex before and after appearance of gyration

BACKGROUND: Mammalian evolution is characterized by a progressive expansion of the surface area of the cerebral cortex, an increase that is accompanied by gyration of the cortical surface. The mechanisms controlling this gyration process are not well characterized but mutational analyses indicate th...

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Autores principales: Nielsen, Karsten B, Kruhøffer, Mogens, Holm, Ida E, Jørgensen, Arne L, Nielsen, Anders L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877059/
https://www.ncbi.nlm.nih.gov/pubmed/20444278
http://dx.doi.org/10.1186/1756-0500-3-127
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author Nielsen, Karsten B
Kruhøffer, Mogens
Holm, Ida E
Jørgensen, Arne L
Nielsen, Anders L
author_facet Nielsen, Karsten B
Kruhøffer, Mogens
Holm, Ida E
Jørgensen, Arne L
Nielsen, Anders L
author_sort Nielsen, Karsten B
collection PubMed
description BACKGROUND: Mammalian evolution is characterized by a progressive expansion of the surface area of the cerebral cortex, an increase that is accompanied by gyration of the cortical surface. The mechanisms controlling this gyration process are not well characterized but mutational analyses indicate that genes involved in neuronal migration play an important function. Due to the lack of gyration of the rodent brain it is important to establish alternative models to examine brain development during the gyration process. The pig brain is gyrated and accordingly is a candidate alternative model. FINDINGS: In this study we have identified genes differentially expressed in the pig cerebral cortex before and after appearance of gyration. Pig cortical tissue from two time points in development representing a non-folded, lissencephalic, brain (embryonic day 60) and primary-folded, gyrencephalic, brain (embryonic day 80) were examined by whole genome expression microarray studies. 91 differentially expressed transcripts (fold change >3) were identified. 84 transcripts were annotated and encoding proteins involved in for example neuronal migration, calcium binding, and cytoskeletal structuring. Quantitative real-time PCR was used to confirm the regulation of a subset of the identified genes. CONCLUSION: This study provides identification of genes which are differentially expressed in the pig cerebral cortex before and after appearance of brain gyration. The identified genes include novel candidate genes which could have functional importance for brain development.
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spelling pubmed-28770592010-05-27 1Identification of genes differentially expressed in the embryonic pig cerebral cortex before and after appearance of gyration Nielsen, Karsten B Kruhøffer, Mogens Holm, Ida E Jørgensen, Arne L Nielsen, Anders L BMC Res Notes Data Note BACKGROUND: Mammalian evolution is characterized by a progressive expansion of the surface area of the cerebral cortex, an increase that is accompanied by gyration of the cortical surface. The mechanisms controlling this gyration process are not well characterized but mutational analyses indicate that genes involved in neuronal migration play an important function. Due to the lack of gyration of the rodent brain it is important to establish alternative models to examine brain development during the gyration process. The pig brain is gyrated and accordingly is a candidate alternative model. FINDINGS: In this study we have identified genes differentially expressed in the pig cerebral cortex before and after appearance of gyration. Pig cortical tissue from two time points in development representing a non-folded, lissencephalic, brain (embryonic day 60) and primary-folded, gyrencephalic, brain (embryonic day 80) were examined by whole genome expression microarray studies. 91 differentially expressed transcripts (fold change >3) were identified. 84 transcripts were annotated and encoding proteins involved in for example neuronal migration, calcium binding, and cytoskeletal structuring. Quantitative real-time PCR was used to confirm the regulation of a subset of the identified genes. CONCLUSION: This study provides identification of genes which are differentially expressed in the pig cerebral cortex before and after appearance of brain gyration. The identified genes include novel candidate genes which could have functional importance for brain development. BioMed Central 2010-05-05 /pmc/articles/PMC2877059/ /pubmed/20444278 http://dx.doi.org/10.1186/1756-0500-3-127 Text en Copyright ©2010 Nielsen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Data Note
Nielsen, Karsten B
Kruhøffer, Mogens
Holm, Ida E
Jørgensen, Arne L
Nielsen, Anders L
1Identification of genes differentially expressed in the embryonic pig cerebral cortex before and after appearance of gyration
title 1Identification of genes differentially expressed in the embryonic pig cerebral cortex before and after appearance of gyration
title_full 1Identification of genes differentially expressed in the embryonic pig cerebral cortex before and after appearance of gyration
title_fullStr 1Identification of genes differentially expressed in the embryonic pig cerebral cortex before and after appearance of gyration
title_full_unstemmed 1Identification of genes differentially expressed in the embryonic pig cerebral cortex before and after appearance of gyration
title_short 1Identification of genes differentially expressed in the embryonic pig cerebral cortex before and after appearance of gyration
title_sort 1identification of genes differentially expressed in the embryonic pig cerebral cortex before and after appearance of gyration
topic Data Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877059/
https://www.ncbi.nlm.nih.gov/pubmed/20444278
http://dx.doi.org/10.1186/1756-0500-3-127
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