Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees
- Autores
- Caporale, Alfredo Leandro; Franchini, Lucia Florencia
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- Understanding the evolution of the human brain is one of the greatest challenges that science faces today. The genetic changes that led to the acquisition of new functional capabilities of our brain are encoded in our genome. Our hypothesis is that the acquisition of new expression patterns in the human lineage of genes involved in the development and functioning of the brain would have been critical for the evolution of our unique cognitive capacities. Using public databases of human accelerated conserved non coding sequences (HAEs or human accelerated elements), we found that the locus of forkhead box P2 (FOXP2) transcription factor contains 6 HAEs, being into the top10 genes with highest number of HAEs, along with some of their putative regulatory targets (RBFOX1, CNTNAP2). Furthermore, this gene has been shown to be critical for normal development of language in humans. Mutations in FOXP2 cause developmental verbal dyspraxia (DVD), and two functional copies of the gene be necessary for a correct development of fluent speech. In this work, we comparatively analyze the 6 HAEs present at this locus through bioinformatics tools, to determine in silico potential transcription factors that would be binding and regulating differentially this gene in humans and chimpanzees. In addition, we functionally characterize these elements through the generation of transgenic zebrafish lines carrying the human or chimpanzee sequence. Through this first approach, we expect to find any difference (gain or loss of function) in the pattern of expression of the reporter protein between orthologs, and to link it to new areas of expression of the FOXP2 gene, and thus may have contributed to the emergence and development of human neuroanatomical features associated with language.
Fil: Caporale, Alfredo Leandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Franchini, Lucia Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
III Taller de Biología Celular y del Desarrollo
Chascomús
Argentina
Instituto Tecnológico de Chascomús - Materia
-
EVOLUTION
BRAIN
FOXP2 - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/236368
Ver los metadatos del registro completo
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Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzeesCaporale, Alfredo LeandroFranchini, Lucia FlorenciaEVOLUTIONBRAINFOXP2https://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Understanding the evolution of the human brain is one of the greatest challenges that science faces today. The genetic changes that led to the acquisition of new functional capabilities of our brain are encoded in our genome. Our hypothesis is that the acquisition of new expression patterns in the human lineage of genes involved in the development and functioning of the brain would have been critical for the evolution of our unique cognitive capacities. Using public databases of human accelerated conserved non coding sequences (HAEs or human accelerated elements), we found that the locus of forkhead box P2 (FOXP2) transcription factor contains 6 HAEs, being into the top10 genes with highest number of HAEs, along with some of their putative regulatory targets (RBFOX1, CNTNAP2). Furthermore, this gene has been shown to be critical for normal development of language in humans. Mutations in FOXP2 cause developmental verbal dyspraxia (DVD), and two functional copies of the gene be necessary for a correct development of fluent speech. In this work, we comparatively analyze the 6 HAEs present at this locus through bioinformatics tools, to determine in silico potential transcription factors that would be binding and regulating differentially this gene in humans and chimpanzees. In addition, we functionally characterize these elements through the generation of transgenic zebrafish lines carrying the human or chimpanzee sequence. Through this first approach, we expect to find any difference (gain or loss of function) in the pattern of expression of the reporter protein between orthologs, and to link it to new areas of expression of the FOXP2 gene, and thus may have contributed to the emergence and development of human neuroanatomical features associated with language.Fil: Caporale, Alfredo Leandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Franchini, Lucia Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaIII Taller de Biología Celular y del DesarrolloChascomúsArgentinaInstituto Tecnológico de ChascomúsInstituto Tecnológico de Chascomús2016info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectTallerBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/236368Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees; III Taller de Biología Celular y del Desarrollo; Chascomús; Argentina; 2016; 36-37CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://tallerbcd.wixsite.com/tallerbcd/taller-2014info:eu-repo/semantics/altIdentifier/url/https://205b7032-7b43-4c7b-9b57-fe88b9455462.filesusr.com/ugd/f7a2bf_51326ccca88443959577921ec1cafd04.pdfNacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:50:10Zoai:ri.conicet.gov.ar:11336/236368instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:50:10.722CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees |
title |
Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees |
spellingShingle |
Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees Caporale, Alfredo Leandro EVOLUTION BRAIN FOXP2 |
title_short |
Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees |
title_full |
Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees |
title_fullStr |
Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees |
title_full_unstemmed |
Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees |
title_sort |
Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees |
dc.creator.none.fl_str_mv |
Caporale, Alfredo Leandro Franchini, Lucia Florencia |
author |
Caporale, Alfredo Leandro |
author_facet |
Caporale, Alfredo Leandro Franchini, Lucia Florencia |
author_role |
author |
author2 |
Franchini, Lucia Florencia |
author2_role |
author |
dc.subject.none.fl_str_mv |
EVOLUTION BRAIN FOXP2 |
topic |
EVOLUTION BRAIN FOXP2 |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Understanding the evolution of the human brain is one of the greatest challenges that science faces today. The genetic changes that led to the acquisition of new functional capabilities of our brain are encoded in our genome. Our hypothesis is that the acquisition of new expression patterns in the human lineage of genes involved in the development and functioning of the brain would have been critical for the evolution of our unique cognitive capacities. Using public databases of human accelerated conserved non coding sequences (HAEs or human accelerated elements), we found that the locus of forkhead box P2 (FOXP2) transcription factor contains 6 HAEs, being into the top10 genes with highest number of HAEs, along with some of their putative regulatory targets (RBFOX1, CNTNAP2). Furthermore, this gene has been shown to be critical for normal development of language in humans. Mutations in FOXP2 cause developmental verbal dyspraxia (DVD), and two functional copies of the gene be necessary for a correct development of fluent speech. In this work, we comparatively analyze the 6 HAEs present at this locus through bioinformatics tools, to determine in silico potential transcription factors that would be binding and regulating differentially this gene in humans and chimpanzees. In addition, we functionally characterize these elements through the generation of transgenic zebrafish lines carrying the human or chimpanzee sequence. Through this first approach, we expect to find any difference (gain or loss of function) in the pattern of expression of the reporter protein between orthologs, and to link it to new areas of expression of the FOXP2 gene, and thus may have contributed to the emergence and development of human neuroanatomical features associated with language. Fil: Caporale, Alfredo Leandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Franchini, Lucia Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina III Taller de Biología Celular y del Desarrollo Chascomús Argentina Instituto Tecnológico de Chascomús |
description |
Understanding the evolution of the human brain is one of the greatest challenges that science faces today. The genetic changes that led to the acquisition of new functional capabilities of our brain are encoded in our genome. Our hypothesis is that the acquisition of new expression patterns in the human lineage of genes involved in the development and functioning of the brain would have been critical for the evolution of our unique cognitive capacities. Using public databases of human accelerated conserved non coding sequences (HAEs or human accelerated elements), we found that the locus of forkhead box P2 (FOXP2) transcription factor contains 6 HAEs, being into the top10 genes with highest number of HAEs, along with some of their putative regulatory targets (RBFOX1, CNTNAP2). Furthermore, this gene has been shown to be critical for normal development of language in humans. Mutations in FOXP2 cause developmental verbal dyspraxia (DVD), and two functional copies of the gene be necessary for a correct development of fluent speech. In this work, we comparatively analyze the 6 HAEs present at this locus through bioinformatics tools, to determine in silico potential transcription factors that would be binding and regulating differentially this gene in humans and chimpanzees. In addition, we functionally characterize these elements through the generation of transgenic zebrafish lines carrying the human or chimpanzee sequence. Through this first approach, we expect to find any difference (gain or loss of function) in the pattern of expression of the reporter protein between orthologs, and to link it to new areas of expression of the FOXP2 gene, and thus may have contributed to the emergence and development of human neuroanatomical features associated with language. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/conferenceObject Taller Book http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
status_str |
publishedVersion |
format |
conferenceObject |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/236368 Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees; III Taller de Biología Celular y del Desarrollo; Chascomús; Argentina; 2016; 36-37 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/236368 |
identifier_str_mv |
Comparative analysis of transcriptional regulation of the FOXP2 gene between humans and chimpanzees; III Taller de Biología Celular y del Desarrollo; Chascomús; Argentina; 2016; 36-37 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://tallerbcd.wixsite.com/tallerbcd/taller-2014 info:eu-repo/semantics/altIdentifier/url/https://205b7032-7b43-4c7b-9b57-fe88b9455462.filesusr.com/ugd/f7a2bf_51326ccca88443959577921ec1cafd04.pdf |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.coverage.none.fl_str_mv |
Nacional |
dc.publisher.none.fl_str_mv |
Instituto Tecnológico de Chascomús |
publisher.none.fl_str_mv |
Instituto Tecnológico de Chascomús |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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13.13397 |