FGFR1 signaling is associated with the magnitude of morphological integration in human head shape
- Autores
- Hünemeier, Tabita; Gómez Valdés, Jorge; de Azevedo, Soledad; Quinto Sanchez, Mirsha Emmanuel; Passaglia, Luciane; Salzano, Francisco M.; Sánchez Mejorada, Gabriela; Acuña Alonzo, Victor; Martínez Abadías, Neus; Bortolini, Maria Catira; Gonzalez José, Rolando
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Objectives: The head can be used as a model to study complex phenotypes controlled simultaneously by morphological integration (MI) due to common factors, and modular patterns caused by local factors affecting the development and functional demands of specific structures. The fibroblast growth factor and receptor system (FGF/ FGFR) participates in cell communication and pattern formation in osseous tissues, among others, and there is compel- ling evidence from mouse model studies suggesting a role of the FGF/FGFR pathway as a covariance-generating signal- ing process in head development. Here we use human data to test if specific genetic variants of another gene of this pathway, the FGFR1 gene, can be associated with differences in the integration of the head. Methods: We explored whether and how three specific variants on FGFR1, previously associated with human cephalic index, influence the pattern and level of head integration of one Native American and one admixed group from Mexico. MI, measured as the intensity of covariation among head traits, was assessed using data from three- dimensional head landmark coordinates taken on 176 individuals. Results: Individuals carrying the derived allele of the rs4647905:G>C polymorphism present significantly greater levels of head MI, especially in facial structures and on the shape space where the modular portion of the covariation is explicitly removed. Conclusions: Since FGFR genes present nonconservative and tissue-specific splicing sites, they may have some effect on protein structure and performance likely involved in developmental processes responsible for the magnitude and pattern of MI in the human head.
Fil: Hünemeier, Tabita. Universidade Federal do Rio Grande do Sul; Brasil
Fil: Gómez Valdés, Jorge. Universidad Nacional Autónoma de México. Facultad de Medicina; México
Fil: de Azevedo, Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; Argentina
Fil: Quinto Sanchez, Mirsha Emmanuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; Argentina
Fil: Passaglia, Luciane. Universidade Federal do Rio Grande do Sul; Brasil
Fil: Salzano, Francisco M.. Universidade Federal do Rio Grande do Sul; Brasil
Fil: Sánchez Mejorada, Gabriela. Universidad Nacional Autónoma de México. Facultad de Medicina; México
Fil: Acuña Alonzo, Victor. Escuela Nacional de Antropología e Historia; México
Fil: Martínez Abadías, Neus. EMBL-CRG Systems Biology Research Unit, Center for Genomic Regulation (CRG); España
Fil: Bortolini, Maria Catira. Universidade Federal do Rio Grande do Sul; Brasil
Fil: Gonzalez José, Rolando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; Argentina - Materia
-
Fgfr1
Human Head Shape
Morphological Integration - 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:11336/7647
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oai:ri.conicet.gov.ar:11336/7647 |
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FGFR1 signaling is associated with the magnitude of morphological integration in human head shapeHünemeier, TabitaGómez Valdés, Jorgede Azevedo, SoledadQuinto Sanchez, Mirsha EmmanuelPassaglia, LucianeSalzano, Francisco M.Sánchez Mejorada, GabrielaAcuña Alonzo, VictorMartínez Abadías, NeusBortolini, Maria CatiraGonzalez José, RolandoFgfr1Human Head ShapeMorphological Integrationhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Objectives: The head can be used as a model to study complex phenotypes controlled simultaneously by morphological integration (MI) due to common factors, and modular patterns caused by local factors affecting the development and functional demands of specific structures. The fibroblast growth factor and receptor system (FGF/ FGFR) participates in cell communication and pattern formation in osseous tissues, among others, and there is compel- ling evidence from mouse model studies suggesting a role of the FGF/FGFR pathway as a covariance-generating signal- ing process in head development. Here we use human data to test if specific genetic variants of another gene of this pathway, the FGFR1 gene, can be associated with differences in the integration of the head. Methods: We explored whether and how three specific variants on FGFR1, previously associated with human cephalic index, influence the pattern and level of head integration of one Native American and one admixed group from Mexico. MI, measured as the intensity of covariation among head traits, was assessed using data from three- dimensional head landmark coordinates taken on 176 individuals. Results: Individuals carrying the derived allele of the rs4647905:G>C polymorphism present significantly greater levels of head MI, especially in facial structures and on the shape space where the modular portion of the covariation is explicitly removed. Conclusions: Since FGFR genes present nonconservative and tissue-specific splicing sites, they may have some effect on protein structure and performance likely involved in developmental processes responsible for the magnitude and pattern of MI in the human head.Fil: Hünemeier, Tabita. Universidade Federal do Rio Grande do Sul; BrasilFil: Gómez Valdés, Jorge. Universidad Nacional Autónoma de México. Facultad de Medicina; MéxicoFil: de Azevedo, Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; ArgentinaFil: Quinto Sanchez, Mirsha Emmanuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; ArgentinaFil: Passaglia, Luciane. Universidade Federal do Rio Grande do Sul; BrasilFil: Salzano, Francisco M.. Universidade Federal do Rio Grande do Sul; BrasilFil: Sánchez Mejorada, Gabriela. Universidad Nacional Autónoma de México. Facultad de Medicina; MéxicoFil: Acuña Alonzo, Victor. Escuela Nacional de Antropología e Historia; MéxicoFil: Martínez Abadías, Neus. EMBL-CRG Systems Biology Research Unit, Center for Genomic Regulation (CRG); EspañaFil: Bortolini, Maria Catira. Universidade Federal do Rio Grande do Sul; BrasilFil: Gonzalez José, Rolando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; ArgentinaWiley2013-12-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/7647Hünemeier, Tabita; Gómez Valdés, Jorge; de Azevedo, Soledad; Quinto Sanchez, Mirsha Emmanuel; Passaglia, Luciane; et al.; FGFR1 signaling is associated with the magnitude of morphological integration in human head shape; Wiley; American Journal of Human Biology; 26; 2; 10-12-2013; 164-1751042-0533enginfo:eu-repo/semantics/altIdentifier/url/http://dx.doi.org/10.1002/ajhb.22496info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/ajhb.22496/abstractinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:01:06Zoai:ri.conicet.gov.ar:11336/7647instacron: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 10:01:06.684CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
FGFR1 signaling is associated with the magnitude of morphological integration in human head shape |
title |
FGFR1 signaling is associated with the magnitude of morphological integration in human head shape |
spellingShingle |
FGFR1 signaling is associated with the magnitude of morphological integration in human head shape Hünemeier, Tabita Fgfr1 Human Head Shape Morphological Integration |
title_short |
FGFR1 signaling is associated with the magnitude of morphological integration in human head shape |
title_full |
FGFR1 signaling is associated with the magnitude of morphological integration in human head shape |
title_fullStr |
FGFR1 signaling is associated with the magnitude of morphological integration in human head shape |
title_full_unstemmed |
FGFR1 signaling is associated with the magnitude of morphological integration in human head shape |
title_sort |
FGFR1 signaling is associated with the magnitude of morphological integration in human head shape |
dc.creator.none.fl_str_mv |
Hünemeier, Tabita Gómez Valdés, Jorge de Azevedo, Soledad Quinto Sanchez, Mirsha Emmanuel Passaglia, Luciane Salzano, Francisco M. Sánchez Mejorada, Gabriela Acuña Alonzo, Victor Martínez Abadías, Neus Bortolini, Maria Catira Gonzalez José, Rolando |
author |
Hünemeier, Tabita |
author_facet |
Hünemeier, Tabita Gómez Valdés, Jorge de Azevedo, Soledad Quinto Sanchez, Mirsha Emmanuel Passaglia, Luciane Salzano, Francisco M. Sánchez Mejorada, Gabriela Acuña Alonzo, Victor Martínez Abadías, Neus Bortolini, Maria Catira Gonzalez José, Rolando |
author_role |
author |
author2 |
Gómez Valdés, Jorge de Azevedo, Soledad Quinto Sanchez, Mirsha Emmanuel Passaglia, Luciane Salzano, Francisco M. Sánchez Mejorada, Gabriela Acuña Alonzo, Victor Martínez Abadías, Neus Bortolini, Maria Catira Gonzalez José, Rolando |
author2_role |
author author author author author author author author author author |
dc.subject.none.fl_str_mv |
Fgfr1 Human Head Shape Morphological Integration |
topic |
Fgfr1 Human Head Shape Morphological Integration |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Objectives: The head can be used as a model to study complex phenotypes controlled simultaneously by morphological integration (MI) due to common factors, and modular patterns caused by local factors affecting the development and functional demands of specific structures. The fibroblast growth factor and receptor system (FGF/ FGFR) participates in cell communication and pattern formation in osseous tissues, among others, and there is compel- ling evidence from mouse model studies suggesting a role of the FGF/FGFR pathway as a covariance-generating signal- ing process in head development. Here we use human data to test if specific genetic variants of another gene of this pathway, the FGFR1 gene, can be associated with differences in the integration of the head. Methods: We explored whether and how three specific variants on FGFR1, previously associated with human cephalic index, influence the pattern and level of head integration of one Native American and one admixed group from Mexico. MI, measured as the intensity of covariation among head traits, was assessed using data from three- dimensional head landmark coordinates taken on 176 individuals. Results: Individuals carrying the derived allele of the rs4647905:G>C polymorphism present significantly greater levels of head MI, especially in facial structures and on the shape space where the modular portion of the covariation is explicitly removed. Conclusions: Since FGFR genes present nonconservative and tissue-specific splicing sites, they may have some effect on protein structure and performance likely involved in developmental processes responsible for the magnitude and pattern of MI in the human head. Fil: Hünemeier, Tabita. Universidade Federal do Rio Grande do Sul; Brasil Fil: Gómez Valdés, Jorge. Universidad Nacional Autónoma de México. Facultad de Medicina; México Fil: de Azevedo, Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; Argentina Fil: Quinto Sanchez, Mirsha Emmanuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; Argentina Fil: Passaglia, Luciane. Universidade Federal do Rio Grande do Sul; Brasil Fil: Salzano, Francisco M.. Universidade Federal do Rio Grande do Sul; Brasil Fil: Sánchez Mejorada, Gabriela. Universidad Nacional Autónoma de México. Facultad de Medicina; México Fil: Acuña Alonzo, Victor. Escuela Nacional de Antropología e Historia; México Fil: Martínez Abadías, Neus. EMBL-CRG Systems Biology Research Unit, Center for Genomic Regulation (CRG); España Fil: Bortolini, Maria Catira. Universidade Federal do Rio Grande do Sul; Brasil Fil: Gonzalez José, Rolando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; Argentina |
description |
Objectives: The head can be used as a model to study complex phenotypes controlled simultaneously by morphological integration (MI) due to common factors, and modular patterns caused by local factors affecting the development and functional demands of specific structures. The fibroblast growth factor and receptor system (FGF/ FGFR) participates in cell communication and pattern formation in osseous tissues, among others, and there is compel- ling evidence from mouse model studies suggesting a role of the FGF/FGFR pathway as a covariance-generating signal- ing process in head development. Here we use human data to test if specific genetic variants of another gene of this pathway, the FGFR1 gene, can be associated with differences in the integration of the head. Methods: We explored whether and how three specific variants on FGFR1, previously associated with human cephalic index, influence the pattern and level of head integration of one Native American and one admixed group from Mexico. MI, measured as the intensity of covariation among head traits, was assessed using data from three- dimensional head landmark coordinates taken on 176 individuals. Results: Individuals carrying the derived allele of the rs4647905:G>C polymorphism present significantly greater levels of head MI, especially in facial structures and on the shape space where the modular portion of the covariation is explicitly removed. Conclusions: Since FGFR genes present nonconservative and tissue-specific splicing sites, they may have some effect on protein structure and performance likely involved in developmental processes responsible for the magnitude and pattern of MI in the human head. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-12-10 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/7647 Hünemeier, Tabita; Gómez Valdés, Jorge; de Azevedo, Soledad; Quinto Sanchez, Mirsha Emmanuel; Passaglia, Luciane; et al.; FGFR1 signaling is associated with the magnitude of morphological integration in human head shape; Wiley; American Journal of Human Biology; 26; 2; 10-12-2013; 164-175 1042-0533 |
url |
http://hdl.handle.net/11336/7647 |
identifier_str_mv |
Hünemeier, Tabita; Gómez Valdés, Jorge; de Azevedo, Soledad; Quinto Sanchez, Mirsha Emmanuel; Passaglia, Luciane; et al.; FGFR1 signaling is associated with the magnitude of morphological integration in human head shape; Wiley; American Journal of Human Biology; 26; 2; 10-12-2013; 164-175 1042-0533 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://dx.doi.org/10.1002/ajhb.22496 info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/ajhb.22496/abstract |
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 |
dc.publisher.none.fl_str_mv |
Wiley |
publisher.none.fl_str_mv |
Wiley |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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13.13397 |