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FGFR1 signaling is associated with the magnitude of morphological integration in human head shape
Author(s) -
Hünemeier Tábita,
GómezValdés Jorge,
Azevedo Soledad,
QuintoSánchez Mirsha,
Passaglia Luciane,
Salzano Francisco M.,
SánchezMejorada Gabriela,
Alonzo Víctor Acuña,
MartínezAbadías Neus,
Bortolini MariaCátira,
GonzálezJosé Rolando
Publication year - 2013
Publication title -
american journal of human biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.559
H-Index - 81
eISSN - 1520-6300
pISSN - 1042-0533
DOI - 10.1002/ajhb.22496
Subject(s) - fibroblast growth factor receptor , fibroblast growth factor receptor 1 , biology , fibroblast growth factor , rna splicing , head (geology) , genetics , phenotype , allele , gene , computational biology , receptor , paleontology , rna
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 compelling evidence from mouse model studies suggesting a role of the FGF/FGFR pathway as a covariance‐generating signaling 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. Am. J. Hum. Biol. 26:164–175, 2014. © 2013 Wiley Periodicals, Inc.