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1.
J Hum Evol ; 90: 176-82, 2016 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-26603101

RESUMEN

Research with extant primate taxa suggests that cochlear labyrinth volume is functionally related to the range of audible frequencies. Specifically, cochlear volume is negatively correlated with both the high and low frequency limits of hearing so that the smaller the cochlea, the higher the normal range of audible frequencies. The close anatomical relationship between the membranous cochlea and the bony cochlear labyrinth allows for the determination of cochlear size from fossil specimens. This study compares Krapina Neandertal cochlear volumes to extant taxa cochlear volumes. Cochlear volumes were acquired from high-resolution computed tomography scans of temporal bones of Krapina Neandertals, chimpanzees, gorillas, and modern humans. We find that Krapina Neandertals' cochlear volumes are similar to modern Homo sapiens and are significantly larger than chimpanzee and gorilla cochlear volumes. The measured cochlear volume in Krapina Neandertals suggests they had a range of audible frequencies similar to the modern human range.


Asunto(s)
Cóclea/anatomía & histología , Fósiles , Hombre de Neandertal/anatomía & histología , Animales , Antropología Física , Tomografía Computarizada por Rayos X
2.
Am J Phys Anthropol ; 154(2): 302-6, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24610299

RESUMEN

Previous studies comparing bony labyrinth morphology in geographically-dispersed samples of Neandertals and modern Homo sapiens (H. sapiens) showed that Neandertals generally have smaller semicircular canals than modern H. sapiens (Hublin et al., ; Spoor et al., ; Glantz et al., ). Here we analyze the morphology of a single group of Neandertal specimens from one locale, the Krapina site, to determine the intraspecific variation in Neandertal semicircular canal sizes. Dimensions of the semicircular canals were collected from computed tomography scans of nine temporal bones. With the rare exception, the dimensions of the semicircular canals in the Krapina sample are similar to those previously reported across a geographically-dispersed sample of Neandertals, further supporting previous studies that suggest low levels of variation in the semicircular canals for Neandertals.


Asunto(s)
Hombre de Neandertal/anatomía & histología , Canales Semicirculares/anatomía & histología , Animales , Imagenología Tridimensional , Canales Semicirculares/diagnóstico por imagen , Hueso Temporal/anatomía & histología , Hueso Temporal/diagnóstico por imagen , Tomografía Computarizada por Rayos X
3.
Am J Med Genet A ; 161A(4): 745-57, 2013 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-23495236

RESUMEN

Craniofacial and neural tissues develop in concert throughout prenatal and postnatal growth. FGFR-related craniosynostosis syndromes, such as Apert syndrome (AS), are associated with specific phenotypes involving both the skull and the brain. We analyzed the effects of the FGFR P253R mutation for AS using the Fgfr2(+/P253R) Apert syndrome mouse to evaluate the effects of this mutation on these two tissues over the course of development from day of birth (P0) to postnatal day 2 (P2). Three-dimensional magnetic resonance microscopy and computed tomography images were acquired from Fgfr2(+/P253R) mice and unaffected littermates at P0 (N = 28) and P2 (N = 20).Three-dimensional coordinate data for 23 skull and 15 brain landmarks were statistically compared between groups. Results demonstrate that the Fgfr2(+/P253R) mice show reduced growth in the facial skeleton and the cerebrum, while the height and width of the neurocranium and caudal regions of the brain show increased growth relative to unaffected littermates. This localized correspondence of differential growth patterns in skull and brain point to their continued interaction through development and suggest that both tissues display divergent postnatal growth patterns relative to unaffected littermates. However, the change in the skull-brain relationship from P0 to P2 implies that each tissue affected by the mutation retains a degree of independence, rather than one tissue directing the development of the other.


Asunto(s)
Acrocefalosindactilia/diagnóstico , Encéfalo/crecimiento & desarrollo , Cráneo/crecimiento & desarrollo , Acrocefalosindactilia/genética , Animales , Antropometría , Modelos Animales de Enfermedad , Imagen por Resonancia Magnética , Ratones , Ratones Transgénicos , Mutación , Tamaño de los Órganos , Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos/genética , Tomografía Computarizada por Rayos X
4.
bioRxiv ; 2023 Feb 27.
Artículo en Inglés | MEDLINE | ID: mdl-36909558

RESUMEN

Phenotypic heterogeneity is a common feature of monogenic neurodevelopmental disorders that can arise from differential severity of missense variants underlying disease, but how distinct alleles impact molecular mechanisms to drive variable disease presentation is not well understood. Here, we investigate missense mutations in the DNA methyltransferase DNMT3A associated with variable overgrowth, intellectual disability, and autism, to uncover molecular correlates of phenotypic heterogeneity in neurodevelopmental disease. We generate a DNMT3A P900L/+ mouse model mimicking a disease mutation with mild-to-moderate severity and compare phenotypic and epigenomic effects with a severe R878H mutation. We show that the P900L mutation leads to disease-relevant overgrowth, obesity, and social deficits shared across DNMT3A disorder models, while the R878H mutation causes more extensive epigenomic disruption leading to differential dysregulation of enhancers elements. We identify distinct gene sets disrupted in each mutant which may contribute to mild or severe disease, and detect shared transcriptomic disruption that likely drives common phenotypes across affected individuals. Finally, we demonstrate that core gene dysregulation detected in DNMT3A mutant mice overlaps effects in other developmental disorder models, highlighting the importance of DNMT3A-deposited methylation in neurodevelopment. Together, these findings define central drivers of DNMT3A disorders and illustrate how variable disruption of transcriptional mechanisms can drive the spectrum of phenotypes in neurodevelopmental disease.

5.
Cell Rep ; 42(11): 113411, 2023 11 28.
Artículo en Inglés | MEDLINE | ID: mdl-37952155

RESUMEN

Phenotypic heterogeneity in monogenic neurodevelopmental disorders can arise from differential severity of variants underlying disease, but how distinct alleles drive variable disease presentation is not well understood. Here, we investigate missense mutations in DNA methyltransferase 3A (DNMT3A), a DNA methyltransferase associated with overgrowth, intellectual disability, and autism, to uncover molecular correlates of phenotypic heterogeneity. We generate a Dnmt3aP900L/+ mouse mimicking a mutation with mild to moderate severity and compare phenotypic and epigenomic effects with a severe R878H mutation. P900L mutants exhibit core growth and behavioral phenotypes shared across models but show subtle epigenomic changes, while R878H mutants display extensive disruptions. We identify mutation-specific dysregulated genes that may contribute to variable disease severity. Shared transcriptomic disruption identified across mutations overlaps dysregulation observed in other developmental disorder models and likely drives common phenotypes. Together, our findings define central drivers of DNMT3A disorders and illustrate how variable epigenomic disruption contributes to phenotypic heterogeneity in neurodevelopmental disease.


Asunto(s)
ADN (Citosina-5-)-Metiltransferasas , ADN Metiltransferasa 3A , Animales , Ratones , ADN (Citosina-5-)-Metiltransferasas/genética , ADN (Citosina-5-)-Metiltransferasas/metabolismo , Epigénesis Genética , Epigenómica , Mutación/genética
6.
Cleft Palate Craniofac J ; 48(4): 394-8, 2011 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20815706

RESUMEN

OBJECTIVE: Craniosynostosis has been hypothesized to result in alterations of the brain and cerebral blood flow due to reduced intracranial volume, potentially leading to cognitive deficits. In this study we test the hypothesis that intracranial volume and whole brain volume in infants with unilateral coronal synostosis differs from those in unaffected infants. DESIGN: Our study sample consists of magnetic resonance images acquired from 7- to 72-week-old infants with right unilateral coronal synostosis prior to surgery (n  =  10) and age-matched unaffected infants (n  =  10). We used Analyze 9.0 software to collect three cranial volume measurements. We used nonparametric tests to determine whether the three measures differ between the two groups. Correlations were calculated between age and the three volume measures in each group to determine whether the growth trajectory of the measurements differ between children with right unicoronal synostosis and unaffected infants. RESULTS: Our results show that the three volume measurements are not reduced in infants with right unicoronal synostosis relative to unaffected children. Correlation analyses between age and various volume measures show similar correlations in infants with right unicoronal synostosis compared with unaffected children. CONCLUSIONS: Our results show that the relationship between brain size and intracranial size in infants with right unicoronal synostosis is similar to that in unaffected children, suggesting that reduced intracranial volume is not responsible for alterations of the brain in craniosynostosis.


Asunto(s)
Encéfalo/patología , Craneosinostosis/patología , Hueso Frontal/anomalías , Hueso Parietal/anomalías , Factores de Edad , Encéfalo/crecimiento & desarrollo , Estudios de Casos y Controles , Suturas Craneales/anomalías , Craneosinostosis/fisiopatología , Humanos , Procesamiento de Imagen Asistido por Computador/métodos , Imagenología Tridimensional/métodos , Lactante , Imagen por Resonancia Magnética/métodos , Tamaño de los Órganos
7.
Dev Dyn ; 239(11): 3058-71, 2010 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-20842696

RESUMEN

Apert syndrome is a congenital disorder caused mainly by two neighboring mutations on fibroblast growth factor receptor 2 (FGFR2). Premature closure of the coronal suture is commonly considered the identifying and primary defect triggering or preceding the additional cranial malformations of Apert phenotype. Here we use two transgenic mouse models of Apert syndrome, Fgfr2(+/S252W) and Fgfr2(+/P253R), to explore variation in cranial phenotypes in newborn (P0) mice. Results show that the facial skeleton is the most affected region of the cranium. Coronal suture patency shows marked variation that is not strongly correlated with skull dysmorphology. The craniofacial effects of the FGFR2 mutations are similar, but Fgfr2(+/S252W) mutant mice display significantly more severe dysmorphology localized to the posterior palate. Our results demonstrate that coronal suture closure is neither the primary nor the sole locus of skull dysmorphology in these mouse models for Apert syndrome, but that the face is also primarily affected.


Asunto(s)
Acrocefalosindactilia/metabolismo , Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos/metabolismo , Acrocefalosindactilia/genética , Animales , Animales Recién Nacidos , Craneosinostosis/genética , Craneosinostosis/metabolismo , Modelos Animales de Enfermedad , Ratones , Ratones Transgénicos , Cráneo/anatomía & histología , Cráneo/embriología
8.
Dev Dyn ; 239(3): 987-97, 2010 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-20077479

RESUMEN

Apert syndrome (AS) is one of at least nine disorders considered members of the fibroblast growth factor receptor (FGFR) -1, -2, and -3-related craniosynostosis syndromes. Nearly 100% of individuals diagnosed with AS carry one of two neighboring mutations on Fgfr2. The cranial phenotype associated with these two mutations includes coronal suture synostosis, either unilateral (unicoronal synostosis) or bilateral (bicoronal synostosis). Brain dysmorphology associated with AS is thought to be secondary to cranial vault or base alterations, but the variation in brain phenotypes within Apert syndrome is unexplained. Here, we present novel three-dimensional data on brain phenotypes of inbred mice at postnatal day 0 each carrying one of the two Fgfr2 mutations associated with AS. Our data suggest that the brain is primarily affected, rather than secondarily responding to skull dysmorphogenesis. Our hypothesis is that the skull and brain are both primarily affected in craniosynostosis and that shared phenogenetic developmental processes affect both tissues in craniosynostosis of Apert syndrome.


Asunto(s)
Acrocefalosindactilia/genética , Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos/metabolismo , Animales , Encéfalo/embriología , Craneosinostosis/genética , Modelos Animales de Enfermedad , Regulación del Desarrollo de la Expresión Génica , Espectroscopía de Resonancia Magnética , Ratones , Ratones Endogámicos C57BL , Ratones Transgénicos , Mutación , Fenotipo , Factores de Tiempo , Tomografía Computarizada por Rayos X/métodos
9.
Nat Commun ; 12(1): 4549, 2021 07 27.
Artículo en Inglés | MEDLINE | ID: mdl-34315901

RESUMEN

Germline pathogenic variants in DNMT3A were recently described in patients with overgrowth, obesity, behavioral, and learning difficulties (DNMT3A Overgrowth Syndrome/DOS). Somatic mutations in the DNMT3A gene are also the most common cause of clonal hematopoiesis, and can initiate acute myeloid leukemia (AML). Using whole genome bisulfite sequencing, we studied DNA methylation in peripheral blood cells of 11 DOS patients and found a focal, canonical hypomethylation phenotype, which is most severe with the dominant negative DNMT3AR882H mutation. A germline mouse model expressing the homologous Dnmt3aR878H mutation phenocopies most aspects of the human DOS syndrome, including the methylation phenotype and an increased incidence of spontaneous hematopoietic malignancies, suggesting that all aspects of this syndrome are caused by this mutation.


Asunto(s)
Anomalías Múltiples/genética , ADN (Citosina-5-)-Metiltransferasas/genética , Epigénesis Genética , Anomalías Múltiples/sangre , Adolescente , Adulto , Animales , Conducta Animal , Peso Corporal/genética , Células de la Médula Ósea/metabolismo , Niño , Preescolar , Islas de CpG/genética , Metilación de ADN/genética , ADN Metiltransferasa 3A , Femenino , Perfilación de la Expresión Génica , Mutación de Línea Germinal/genética , Hematopoyesis/genética , Células Madre Hematopoyéticas/metabolismo , Humanos , Lactante , Leucemia/genética , Leucemia/patología , Masculino , Ratones Endogámicos C57BL , Obesidad/genética , Fenotipo , Síndrome , Transcripción Genética
10.
BMC Dev Biol ; 10: 22, 2010 Feb 22.
Artículo en Inglés | MEDLINE | ID: mdl-20175913

RESUMEN

BACKGROUND: Apert syndrome is characterized by craniosynostosis and limb abnormalities and is primarily caused by FGFR2 +/P253R and +/S252W mutations. The former mutation is present in approximately one third whereas the latter mutation is present in two-thirds of the patients with this condition. We previously reported an inbred transgenic mouse model with the Fgfr2 +/S252W mutation on the C57BL/6J background for Apert syndrome. Here we present a mouse model for the Fgfr2+/P253R mutation. RESULTS: We generated inbred Fgfr2(+/P253R) mice on the same C56BL/6J genetic background and analyzed their skeletal abnormalities. 3D micro-CT scans of the skulls of the Fgfr2(+/P253R) mice revealed that the skull length was shortened with the length of the anterior cranial base significantly shorter than that of the Fgfr2(+/S252W) mice at P0. The Fgfr2(+/P253R) mice presented with synostosis of the coronal suture and proximate fronts with disorganized cellularity in sagittal and lambdoid sutures. Abnormal osteogenesis and proliferation were observed at the developing coronal suture and long bones of the Fgfr2(+/P253R) mice as in the Fgfr2(+/S252W) mice. Activation of mitogen-activated protein kinases (MAPK) was observed in the Fgfr2(+/P253R) neurocranium with an increase in phosphorylated p38 as well as ERK1/2, whereas phosphorylated AKT and PKCalpha were not obviously changed as compared to those of wild-type controls. There were localized phenotypic and molecular variations among individual embryos with different mutations and among those with the same mutation. CONCLUSIONS: Our in vivo studies demonstrated that the Fgfr2 +/P253R mutation resulted in mice with cranial features that resemble those of the Fgfr2(+/S252W) mice and human Apert syndrome. Activated p38 in addition to the ERK1/2 signaling pathways may mediate the mutant neurocranial phenotype. Though Apert syndrome is traditionally thought to be a consistent phenotype, our results suggest localized and regional variations in the phenotypes that characterize Apert syndrome.


Asunto(s)
Acrocefalosindactilia/metabolismo , Modelos Animales de Enfermedad , Sistema de Señalización de MAP Quinasas , Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos/genética , Cráneo/anomalías , Proteínas Quinasas p38 Activadas por Mitógenos/metabolismo , Sustitución de Aminoácidos , Animales , Ratones , Ratones Endogámicos C57BL , Cráneo/metabolismo
11.
Cell Rep ; 33(8): 108416, 2020 11 24.
Artículo en Inglés | MEDLINE | ID: mdl-33238114

RESUMEN

Mutations in DNA methyltransferase 3A (DNMT3A) have been detected in autism and related disorders, but how these mutations disrupt nervous system function is unknown. Here, we define the effects of DNMT3A mutations associated with neurodevelopmental disease. We show that diverse mutations affect different aspects of protein activity but lead to shared deficiencies in neuronal DNA methylation. Heterozygous DNMT3A knockout mice mimicking DNMT3A disruption in disease display growth and behavioral alterations consistent with human phenotypes. Strikingly, in these mice, we detect global disruption of neuron-enriched non-CG DNA methylation, a binding site for the Rett syndrome protein MeCP2. Loss of this methylation leads to enhancer and gene dysregulation that overlaps with models of Rett syndrome and autism. These findings define the effects of DNMT3A haploinsufficiency in the brain and uncover disruption of the non-CG methylation pathway as a convergence point across neurodevelopmental disorders.


Asunto(s)
ADN Metiltransferasa 3A/metabolismo , Epigenómica/métodos , Trastornos del Neurodesarrollo/genética , Animales , Haploinsuficiencia , Humanos , Ratones
12.
Am J Med Genet A ; 149A(10): 2158-65, 2009 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-19764029

RESUMEN

Ts65Dn mice have segmental trisomy for orthologs of about half of the genes on human chromosome 21, including Ets2. These mice develop anomalies of the cranial skeleton and thymus that parallel those in Down syndrome. Overexpression of the Ets2 transcription factor gene was posited to be sufficient to produce these craniofacial and thymus deficits in transgenic mice that constitutively overexpress a processed Ets2 transcript under a promiscuous promoter [Sumarsono et al. (1996); Nature 379:534-537; Wolvetang et al. (2003); Hum Mol Genet 12:247-255]. Evaluation of trisomic mice with varying copy numbers of a properly regulated Ets2 gene indicated increased dosage of Ets2 was not sufficient to produce effects on thymus and most of the cranial anomalies seen in Ts65Dn mice. However, mesoderm-derived cranial skeletal elements are significantly more affected in Ts65Dn, Ets2(+/-) mice compared to Ts65Dn littermates suggesting a differential interaction of Ets2-related processes with mesoderm-derived and neural crest-derived formative tissues. Our results support the growing evidence for interactions among multiple genes contributing to developmental perturbations resulting in variation in complex Down syndrome phenotypes.


Asunto(s)
Anomalías Craneofaciales/genética , Síndrome de Down/patología , Ratones Transgénicos , Proteína Proto-Oncogénica c-ets-2/fisiología , Timo/anomalías , Anomalías Múltiples/embriología , Anomalías Múltiples/genética , Anomalías Múltiples/patología , Animales , Simulación por Computador , Anomalías Craneofaciales/complicaciones , Anomalías Craneofaciales/embriología , Anomalías Craneofaciales/patología , Modelos Animales de Enfermedad , Síndrome de Down/complicaciones , Síndrome de Down/genética , Ratones , Ratones Endogámicos C3H , Ratones Endogámicos C57BL , Modelos Anatómicos , Fenotipo , Proteína Proto-Oncogénica c-ets-2/genética , Cráneo/patología , Timo/patología
13.
Transfus Clin Biol ; 11(1): 33-9, 2004 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-14980547

RESUMEN

Accidental transfusion of ABO-incompatible red blood cells (RBCs) is a leading cause of fatal transfusion reactions. To prevent this and to create a universal blood supply, the idea of converting blood group A and B antigens to H using specific exo-glycosidases capable of removing the immunodominant sugar residues was pioneered by Goldstein and colleagues at the New York Blood Center in the early 1980s. Conversion of group B RBCs to O was initially carried out with alpha-galactosidase extracted from coffee beans. These enzyme-converted O (ECO) RBCs appeared to survive normally in all recipients independent of blood group. The clinical trials moved from small infusions to single RBC units and finally multiple and repeated transfusions. A successful phase II trial utilizing recombinant enzyme was reported by Kruskall and colleagues in 2000. Enzymatic conversion of group A RBCs has lagged behind due to lack of appropriate glycosidases and the more complex nature of A antigens. Identification of novel bacterial glycosidases with improved kinetic properties and specificities for the A and B antigens has greatly advanced the field. Conversion of group A RBCs can be achieved with improved glycosidases and the conversion conditions for both A and B antigens optimized to use more cost-efficient quantities of enzymes and gentler conditions including neutral pH and short incubation times at room temperature. Of the different strategies envisioned to create a universal blood supply, the ECO concept is the only one, for which human clinical trials have been performed. This paper discusses some biochemical and clinical aspects of this developing technology.


Asunto(s)
Incompatibilidad de Grupos Sanguíneos/prevención & control , Membrana Eritrocítica/inmunología , Glicósido Hidrolasas/farmacología , Isoantígenos/efectos de los fármacos , Oligosacáridos/metabolismo , Trisacáridos/metabolismo , Sistema del Grupo Sanguíneo ABO , Proteínas Bacterianas/farmacología , Tipificación y Pruebas Cruzadas Sanguíneas , Ensayos Clínicos como Asunto , Membrana Eritrocítica/efectos de los fármacos , Predicción , Proteínas Fúngicas/farmacología , Humanos , Isoantígenos/metabolismo , Oligosacáridos de Cadena Ramificada , Especificidad por Sustrato , Reacción a la Transfusión
14.
Anat Rec (Hoboken) ; 294(7): 1103-15, 2011 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-21618436

RESUMEN

Pneumatization of the temporal bone is often included in descriptions of fossils and as a phylogenetic marker, but a number of questions about the evolution, growth, and development of the trait remain. Many studies have analyzed temporal bone pneumatization from a clinical perspective, but a systematic quantification of normal development of pneumatized spaces has not been conducted. In this study, ontogenetic change in the size and organization of temporal bone pneumatization is analyzed in a cross-sectional sample of humans. High resolution computed tomography scans of the temporal bone were acquired from a cross-sectional sample of humans (N = 28). Bone volume fractions, anisotropy, trabecular number, trabecular thickness, surface area, and volume were analyzed to provide information about the organization and size of pneumatized spaces across ontogeny. The results indicate that there are general and region-specific patterns of ontogenetic changes in the organization of pneumatized spaces. These changes reflect the transition from nonpneumatized bone to pneumatized bone. It also demonstrates that those regions that are pneumatized early in ontogeny (such as the mastoid antrum) continue to remodel after the initial period of pneumatization. The dynamic nature of temporal bone pneumatization over ontogeny suggests that this character requires careful consideration when used as a character for phylogenetic analyses. These results demonstrate the importance of comparing individuals from similar developmental stages, especially when completing quantitative analyses of the extent of pneumatization or organization of the spaces.


Asunto(s)
Apófisis Mastoides/anatomía & histología , Hueso Temporal/anatomía & histología , Adolescente , Adulto , Anatomía Transversal , Evolución Biológica , Niño , Preescolar , Humanos , Procesamiento de Imagen Asistido por Computador , Lactante , Recién Nacido , Apófisis Mastoides/diagnóstico por imagen , Filogenia , Hueso Temporal/diagnóstico por imagen , Tomografía Computarizada por Rayos X , Adulto Joven
15.
J Hum Evol ; 55(4): 682-90, 2008 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-18715622

RESUMEN

Temporal bone pneumatization has been included in lists of characters used in phylogenetic analyses of human evolution. While studies suggest that the extent of pneumatization has decreased over the course of human evolution, little is known about the processes underlying these changes or their significance. In short, reasons for the observed reduction and the potential reorganization within pneumatized spaces are unknown. Technological limitations have limited previous analyses of pneumatization in extant and fossil species to qualitative observations of the extent of temporal bone pneumatization. In this paper, we introduce a novel application of quantitative methods developed for the study of trabecular bone to the analysis of pneumatized spaces of the temporal bone. This method utilizes high-resolution X-ray computed tomography (HRXCT) images and quantitative software to estimate three-dimensional parameters (bone volume fractions, anisotropy, and trabecular thickness) of bone structure within defined units of pneumatized spaces. We apply this approach in an analysis of temporal bones of diverse but related primate species, Gorilla gorilla, Pan troglodytes, Homo sapiens, and Papio hamadryas anubis, to illustrate the potential of these methods. In demonstrating the utility of these methods, we show that there are interspecific differences in the bone structure of pneumatized spaces, perhaps reflecting changes in the localized growth dynamics, location of muscle attachments, encephalization, or basicranial flexion.


Asunto(s)
Catarrinos/anatomía & histología , Imagenología Tridimensional/métodos , Hueso Temporal/anatomía & histología , Animales , Femenino , Humanos , Masculino , Tomografía Computarizada por Rayos X
16.
J Anat ; 210(4): 394-405, 2007 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-17428201

RESUMEN

Adult craniofacial morphology results from complex interactions among genetic, epigenetic and environmental factors. Trisomy causes perturbations in the genetic programmes that control development and these are reflected in morphology that can either ameliorate or worsen with time and growth. Many of the specific changes that occur in Down syndrome can be studied in the Ts65Dn trisomic mouse, which shows direct parallels with specific aspects of adult craniofacial dysmorphology associated with trisomy 21. This study investigates patterns of craniofacial growth in Ts65Dn mice and their euploid littermates to assess how the adult dysmorphology develops. Three-dimensional coordinate data were collected from microcomputed tomography scans of the face, cranial base, palate and mandible of newborn (P0) and adult trisomic and euploid mice. Growth patterns were analysed using Euclidean distance matrix analysis. P0 trisomic mice show significant differences in craniofacial shape. Growth is reduced along the rostro-caudal axis of the Ts65Dn face and palate relative to euploid littermates and Ts65Dn mandibles demonstrate reduced growth local to the mandibular processes. Thus, the features of Down syndrome that are reflected in the mature Ts65Dn skull are established early in development and growth does not appear to ameliorate them. Differences in growth may in fact contribute to many of the morphological differences that are evident at birth in trisomic mice and humans.


Asunto(s)
Aneuploidia , Síndrome de Down/embriología , Cráneo/embriología , Animales , Femenino , Desarrollo Fetal/fisiología , Edad Gestacional , Imagenología Tridimensional , Masculino , Mandíbula/embriología , Ratones , Ratones Mutantes , Modelos Animales , Hueso Paladar/embriología , Tomografía Computarizada por Rayos X
17.
Development ; 132(15): 3537-48, 2005 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-15975938

RESUMEN

Apert syndrome is an autosomal dominant disorder characterized by malformations of the skull, limbs and viscera. Two-thirds of affected individuals have a S252W mutation in fibroblast growth factor receptor 2 (FGFR2). To study the pathogenesis of this condition, we generated a knock-in mouse model with this mutation. The Fgfr2(+/S252W) mutant mice have abnormalities of the skeleton, as well as of other organs including the brain, thymus, lungs, heart and intestines. In the mutant neurocranium, we found a midline sutural defect and craniosynostosis with abnormal osteoblastic proliferation and differentiation. We noted ectopic cartilage at the midline sagittal suture, and cartilage abnormalities in the basicranium, nasal turbinates and trachea. In addition, from the mutant long bones, in vitro cell cultures grown in osteogenic medium revealed chondrocytes, which were absent in the controls. Our results suggest that altered cartilage and bone development play a significant role in the pathogenesis of the Apert syndrome phenotype.


Asunto(s)
Acrocefalosindactilia/genética , Huesos/anomalías , Cartílago/anomalías , Proteínas Tirosina Quinasas Receptoras/genética , Receptores de Factores de Crecimiento de Fibroblastos/genética , Sustitución de Aminoácidos , Animales , Desarrollo Óseo , Cartílago/crecimiento & desarrollo , Modelos Animales de Enfermedad , Exones , Humanos , Ratones , Ratones Transgénicos , Mutagénesis Sitio-Dirigida , Polimorfismo de Nucleótido Simple , Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos
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