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1.
Genes Dev ; 26(8): 785-90, 2012 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-22508725

RESUMEN

Plants sense neighbor proximity as a decrease in the ratio of red to far-red light, which triggers a series of developmental responses. In Arabidopsis, phytochrome B (PHYB) is the major sensor of shade, but PHYB excitation has not been linked directly to a growth response. We show that the basic helix-loop-helix (bHLH) transcription factor PIF7 (phytochrome-interacting factor 7), an interactor of PHYB, accumulates in its dephosphorylated form in shade, allowing it to bind auxin biosynthetic genes and increase their expression. New auxin synthesized through a PIF7-regulated pathway is required for shade-induced growth, linking directly the perception of a light quality signal to a rapid growth response.


Asunto(s)
Proteínas de Arabidopsis/metabolismo , Arabidopsis/crecimiento & desarrollo , Proteínas de Unión al ADN/metabolismo , Ácidos Indolacéticos/metabolismo , Arabidopsis/anatomía & histología , Arabidopsis/genética , Proteínas de Arabidopsis/genética , Proteínas de Unión al ADN/genética , Expresión Génica/efectos de los fármacos , Regulación de la Expresión Génica de las Plantas , Ácidos Indolacéticos/farmacología , Luz , Mutación , Fitocromo B/metabolismo
2.
Science ; 342(6158): 632-7, 2013 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-24179226

RESUMEN

We used single-cell genomic approaches to map DNA copy number variation (CNV) in neurons obtained from human induced pluripotent stem cell (hiPSC) lines and postmortem human brains. We identified aneuploid neurons, as well as numerous subchromosomal CNVs in euploid neurons. Neurotypic hiPSC-derived neurons had larger CNVs than fibroblasts, and several large deletions were found in hiPSC-derived neurons but not in matched neural progenitor cells. Single-cell sequencing of endogenous human frontal cortex neurons revealed that 13 to 41% of neurons have at least one megabase-scale de novo CNV, that deletions are twice as common as duplications, and that a subset of neurons have highly aberrant genomes marked by multiple alterations. Our results show that mosaic CNV is abundant in human neurons.


Asunto(s)
Variaciones en el Número de Copia de ADN , Lóbulo Frontal/citología , Mosaicismo , Células-Madre Neurales/citología , Neuronas/citología , Aneuploidia , Humanos , Células Madre Pluripotentes Inducidas/citología , Masculino , Neurogénesis , Análisis de Secuencia de ADN , Eliminación de Secuencia , Análisis de la Célula Individual
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