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2.
Wellcome Open Res ; 8: 507, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-38046191

RESUMEN

We present a genome assembly from an individual male Anopheles moucheti (the malaria mosquito; Arthropoda; Insecta; Diptera; Culicidae), from a wild population in Cameroon. The genome sequence is 271 megabases in span. The majority of the assembly is scaffolded into three chromosomal pseudomolecules with the X sex chromosome assembled. The complete mitochondrial genome was also assembled and is 15.5 kilobases in length.

3.
Curr Biol ; 26(5): 654-60, 2016 Mar 07.
Artículo en Inglés | MEDLINE | ID: mdl-26923788

RESUMEN

While components of the pathway that establishes left-right asymmetry have been identified in diverse animals, from vertebrates to flies, it is striking that the genes involved in the first symmetry-breaking step remain wholly unknown in the most obviously chiral animals, the gastropod snails. Previously, research on snails was used to show that left-right signaling of Nodal, downstream of symmetry breaking, may be an ancestral feature of the Bilateria [1 and 2]. Here, we report that a disabling mutation in one copy of a tandemly duplicated, diaphanous-related formin is perfectly associated with symmetry breaking in the pond snail. This is supported by the observation that an anti-formin drug treatment converts dextral snail embryos to a sinistral phenocopy, and in frogs, drug inhibition or overexpression by microinjection of formin has a chirality-randomizing effect in early (pre-cilia) embryos. Contrary to expectations based on existing models [3, 4 and 5], we discovered asymmetric gene expression in 2- and 4-cell snail embryos, preceding morphological asymmetry. As the formin-actin filament has been shown to be part of an asymmetry-breaking switch in vitro [6 and 7], together these results are consistent with the view that animals with diverse body plans may derive their asymmetries from the same intracellular chiral elements [8].


Asunto(s)
Tipificación del Cuerpo , Proteínas Fetales/genética , Lymnaea/genética , Proteínas de Microfilamentos/genética , Proteínas Nucleares/genética , Transducción de Señal , Xenopus laevis/genética , Animales , Proteínas Fetales/metabolismo , Forminas , Lymnaea/embriología , Lymnaea/metabolismo , Proteínas de Microfilamentos/metabolismo , Proteínas Nucleares/metabolismo , Fenotipo , Xenopus laevis/embriología , Xenopus laevis/metabolismo
4.
Nat Commun ; 1: 98, 2010 Oct 19.
Artículo en Inglés | MEDLINE | ID: mdl-20981026

RESUMEN

Biodiversity is of crucial importance for ecosystem functioning, sustainability and resilience, but the magnitude and organization of marine diversity at a range of spatial and taxonomic scales are undefined. In this paper, we use second-generation sequencing to unmask putatively diverse marine metazoan biodiversity in a Scottish temperate benthic ecosystem. We show that remarkable differences in diversity occurred at microgeographical scales and refute currently accepted ecological and taxonomic paradigms of meiofaunal identity, rank abundance and concomitant understanding of trophic dynamics. Richness estimates from the current benchmarked Operational Clustering of Taxonomic Units from Parallel UltraSequencing analyses are broadly aligned with those derived from morphological assessments. However, the slope of taxon rarefaction curves for many phyla remains incomplete, suggesting that the true alpha diversity is likely to exceed current perceptions. The approaches provide a rapid, objective and cost-effective taxonomic framework for exploring links between ecosystem structure and function of all hitherto intractable, but ecologically important, communities.


Asunto(s)
Biodiversidad , Análisis de Secuencia de ADN/métodos , Animales , Biología Computacional , Biología Marina , Filogenia , Reacción en Cadena de la Polimerasa
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