Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros












Base de datos
Intervalo de año de publicación
1.
Biochim Biophys Acta Biomembr ; 1859(3): 402-414, 2017 03.
Artículo en Inglés | MEDLINE | ID: mdl-27916633

RESUMEN

Connexins or innexins form gap junctions, while claudins and occludins form tight junctions. In this study, statistical data, derived using novel software, indicate that these four junctional protein families and eleven other families of channel and channel auxiliary proteins are related by common descent and comprise the Tetraspan (4 TMS) Junctional Complex (4JC) Superfamily. These proteins all share similar 4 transmembrane α-helical (TMS) topologies. Evidence is presented that they arose via an intragenic duplication event, whereby a 2 TMS-encoding genetic element duplicated tandemly to give 4 TMS proteins. In cases where high resolution structural data were available, the conclusion of homology was supported by conducting structural comparisons. Phylogenetic trees reveal the probable relationships of these 15 families to each other. Long homologues containing fusions to other recognizable domains as well as internally duplicated or fused domains are reported. Large "fusion" proteins containing 4JC domains proved to fall predominantly into family-specific patterns as follows: (1) the 4JC domain was N-terminal; (2) the 4JC domain was C-terminal; (3) the 4JC domain was duplicated or occasionally triplicated and (4) mixed fusion types were present. Our observations provide insight into the evolutionary origins and subfunctions of these proteins as well as guides concerning their structural and functional relationships.


Asunto(s)
Proteínas de la Membrana/química , Secuencia de Aminoácidos , Animales , Claudinas/química , Claudinas/clasificación , Conexinas/química , Conexinas/clasificación , Uniones Comunicantes/metabolismo , Proteínas de la Membrana/clasificación , Proteínas Proteolipídicas Asociadas a Mielina y Linfocito/química , Proteínas Proteolipídicas Asociadas a Mielina y Linfocito/clasificación , Filogenia , Estructura Terciaria de Proteína , Alineación de Secuencia , Uniones Estrechas/metabolismo
2.
BMC Genomics ; 16: 431, 2015 Jun 05.
Artículo en Inglés | MEDLINE | ID: mdl-26044654

RESUMEN

BACKGROUND: Domestic goats (Capra hircus) have been selected to play an essential role in agricultural production systems, since being domesticated from their wild progenitor, bezoar (Capra aegagrus). A detailed understanding of the genetic consequences imparted by the domestication process remains a key goal of evolutionary genomics. RESULTS: We constructed the reference genome of bezoar and sequenced representative breeds of domestic goats to search for genomic changes that likely have accompanied goat domestication and breed formation. Thirteen copy number variation genes associated with coat color were identified in domestic goats, among which ASIP gene duplication contributes to the generation of light coat-color phenotype in domestic goats. Analysis of rapidly evolving genes identified genic changes underlying behavior-related traits, immune response and production-related traits. CONCLUSION: Based on the comparison studies of copy number variation genes and rapidly evolving genes between wild and domestic goat, our findings and methodology shed light on the genetic mechanism of animal domestication and will facilitate future goat breeding.


Asunto(s)
Genoma , Cabras/genética , Secuencia de Aminoácidos , Animales , Animales Domésticos/genética , Animales Salvajes/genética , Evolución Biológica , Cruzamiento , ADN/análisis , ADN/aislamiento & purificación , Variaciones en el Número de Copia de ADN , Variación Genética , Sistema Inmunológico/metabolismo , Masculino , Datos de Secuencia Molecular , Proteínas Proteolipídicas Asociadas a Mielina y Linfocito/clasificación , Proteínas Proteolipídicas Asociadas a Mielina y Linfocito/genética , Sistema Nervioso/metabolismo , Filogenia , Estructura Terciaria de Proteína , Receptor de Colecistoquinina A/química , Receptor de Colecistoquinina A/genética , Receptor de Colecistoquinina A/metabolismo , Alineación de Secuencia
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...