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1.
Neuron ; 81(6): 1255-1262, 2014 Mar 19.
Artículo en Inglés | MEDLINE | ID: mdl-24583023

RESUMEN

Major nonprimate-primate differences in cortico-genesis include the dimensions, precursor lineages, and developmental timing of the germinal zones (GZs). microRNAs (miRNAs) of laser-dissected GZ compartments and cortical plate (CP) from embryonic E80 macaque visual cortex were deep sequenced. The CP and the GZ including ventricular zone (VZ) and outer and inner subcompartments of the outer subventricular zone (OSVZ) in area 17 displayed unique miRNA profiles. miRNAs present in primate, but absent in rodent, contributed disproportionately to the differential expression between GZ subregions. Prominent among the validated targets of these miRNAs were cell-cycle and neurogenesis regulators. Coevolution between the emergent miRNAs and their targets suggested that novel miRNAs became integrated into ancient gene circuitry to exert additional control over proliferation. We conclude that multiple cell-cycle regulatory events contribute to the emergence of primate-specific cortical features, including the OSVZ, generated enlarged supragranular layers, largely responsible for the increased primate cortex computational abilities.


Asunto(s)
Ciclo Celular/genética , Regulación de la Expresión Génica , Macaca/genética , MicroARNs/genética , Neurogénesis/genética , Neuronas/citología , Corteza Visual/citología , Animales , Ciclo Celular/fisiología , Evolución Molecular , Femenino , Neurogénesis/fisiología , Neuronas/metabolismo , Corteza Visual/metabolismo
2.
Alzheimers Dement ; 10(5 Suppl): S277-S283.e10, 2014 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-24239249

RESUMEN

BACKGROUND: A mutation in presenilin 1 (E280A) causes early-onset Alzheimer's disease. Understanding the origin of this mutation will inform medical genetics. METHODS: We sequenced the genomes of 102 individuals from Antioquia, Colombia. We applied identity-by-descent analysis to identify regions of common ancestry. We estimated the age of the E280A mutation and the local ancestry of the haplotype harboring this mutation. RESULTS: All affected individuals share a minimal haplotype of 1.8 Mb containing E280A. We estimate a time to most recent common ancestor of E280A of 10 (95% credible interval, 7.2-12.6) generations. We date the de novo mutation event to 15 (95% credible interval, 11-25) generations ago. We infer a western European geographic origin of the shared haplotype. CONCLUSIONS: The age and geographic origin of E280A are consistent with a single founder dating from the time of the Spanish Conquistadors who began colonizing Colombia during the early 16th century.


Asunto(s)
Enfermedad de Alzheimer/genética , Predisposición Genética a la Enfermedad , Mutación , Presenilina-1/genética , Edad de Inicio , Colombia , Efecto Fundador , Haplotipos , Humanos , Patrón de Herencia , Población Blanca/genética
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