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1.
Proc Natl Acad Sci U S A ; 118(28)2021 07 13.
Artículo en Inglés | MEDLINE | ID: mdl-34244441

RESUMEN

Ultrasonic hearing and vocalization are the physiological mechanisms controlling echolocation used in hunting and navigation by microbats and bottleneck dolphins and for social communication by mice and rats. The molecular and cellular basis for ultrasonic hearing is as yet unknown. Here, we show that knockout of the mechanosensitive ion channel PIEZO2 in cochlea disrupts ultrasonic- but not low-frequency hearing in mice, as shown by audiometry and acoustically associative freezing behavior. Deletion of Piezo2 in outer hair cells (OHCs) specifically abolishes associative learning in mice during hearing exposure at ultrasonic frequencies. Ex vivo cochlear Ca2+ imaging has revealed that ultrasonic transduction requires both PIEZO2 and the hair-cell mechanotransduction channel. The present study demonstrates that OHCs serve as effector cells, combining with PIEZO2 as an essential molecule for ultrasonic hearing in mice.


Asunto(s)
Células Ciliadas Auditivas Externas/metabolismo , Audición/fisiología , Canales Iónicos/metabolismo , Ultrasonido , Animales , Calcio/metabolismo , Reacción Cataléptica de Congelación , Eliminación de Gen , Células HEK293 , Humanos , Mecanotransducción Celular , Ratones Noqueados
2.
Mitochondrial DNA A DNA Mapp Seq Anal ; 27(4): 2635-6, 2016 07.
Artículo en Inglés | MEDLINE | ID: mdl-26024147

RESUMEN

The complete chloroplast genome (cpDNA) sequence of an endemic conifer species, Armand pine Pinus armandii Franch., is determined in this study. The cpDNA was 117,265 bp in length, containing a pair of 475 bp inverted repeat (IR) regions those distinguished in large and small single copy (LSC and SSC) regions of 64,548 and 51,767 bp in length, respectively. The cpDNA contained 114 genes, including 74 protein-coding genes (74 PCG species), 4 ribosomal RNA genes (four rRNA species) and 36 transfer RNA genes (33 tRNA species). Out of these genes, 12 harbor a single intron and most of the genes occurred in a single copy. The overall AT content of the Armand pine cpDNA was 61.2%, while the corresponding values of the LSC, SSC and IR regions were 62.0%, 60.2% and 62.7%, respectively. A phylogenetic analysis revealed that P. armandii chloroplast genome is closely related to that of the P. koraiensis within the genus Pinus.


Asunto(s)
Genoma del Cloroplasto/genética , Genoma de Planta/genética , Pinus/genética , ARN Ribosómico/genética , Secuencia Rica en At/genética , China , ADN de Cloroplastos/genética , Genoma Mitocondrial/genética , Filogenia , Pinus/clasificación , ARN de Transferencia/genética , Análisis de Secuencia de ADN/métodos
3.
Mitochondrial DNA A DNA Mapp Seq Anal ; 27(4): 2732-3, 2016 07.
Artículo en Inglés | MEDLINE | ID: mdl-26057016

RESUMEN

The complete nucleotide sequence of the Taiwan red pine Pinus taiwanensis Hayata chloroplast genome (cpDNA) is determined in this study. The genome is composed of 119,741 bp in length, containing a pair of very short inverted repeat (IRa and IRb) regions of 495 bp, which was divided by a large single-copy (LSC) region of 65,670 bp and a small single-copy (SSC) region of 53,080 bp in length. The cpDNA contained 115 genes, including 74 protein-coding genes (73 PCG species), 4 ribosomal RNA genes (four rRNA species) and 37 tRNA genes (22 tRNA species). Out of these genes, 12 harbored a single intron, and one (rps12) contained a couple of introns. The overall AT content of the Taiwan red pine cpDNA is 61.5%, while the corresponding values of the LSC, SSC and IR regions are 62.2%, 60.6% and 63.6%, respectively. A maximum parsimony phylogenetic analysis suggested that the genus Pinus, Picea, Abies and Larix were strongly supported as monophyletic, and the cpDNA of P. taiwanensis is closely related to that of P. thunbergii.


Asunto(s)
Genoma del Cloroplasto/genética , Pinaceae/genética , ADN de Cloroplastos/genética , Orden Génico/genética , Genoma Mitocondrial/genética , Genoma de Planta/genética , Filogenia , Pinaceae/clasificación , ARN Ribosómico/genética , Análisis de Secuencia de ADN , Taiwán
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