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1.
Cell Metab ; 36(1): 7-9, 2024 01 02.
Artículo en Inglés | MEDLINE | ID: mdl-38171339

RESUMEN

Spinal cord-associated disorders are common in the elderly population; however, the mechanisms underlying spinal aging remain elusive. In a recent Nature paper, Sun et al. systemically analyzed aged spines in nonhuman primates and identified a new cluster of CHIT1-positive microglia that drives motor neuron senescence and subsequent spine aging.


Asunto(s)
Neuronas Motoras , Médula Espinal , Animales , Humanos , Anciano , Envejecimiento/fisiología , Microglía
2.
Zool Res ; 39(6): 431-436, 2018 Nov 18.
Artículo en Inglés | MEDLINE | ID: mdl-30084433

RESUMEN

Three-finger toxins (TFTs) are well-recognized non-enzymatic venom proteins found in snakes. However, although TFTs exhibit accelerated evolution, the drivers of this evolution remain poorly understood. The structural complexes between long-chain α-neurotoxins, a subfamily of TFTs, and their nicotinic acetylcholine receptor targets have been determined in previous research, providing an opportunity to address such questions. In the current study, we observed several previously identified positively selected sites (PSSs) and the highly variable C-terminal loop of these toxins at the toxin/receptor interface. Of interest, analysis of the molecular adaptation of the toxin-recognition regions in the corresponding receptors provided no statistical evidence for positive selection. However, these regions accumulated abundant amino acid variations in the receptors from the prey of snakes, suggesting that accelerated substitution of TFTs could be a consequence of adaptation to these variations. To the best of our knowledge, this atypical evolution, initially discovered in scorpions, is reported in snake toxins for the first time and may be applicable for the evolution of toxins from other venomous animals.


Asunto(s)
Venenos de Serpiente/genética , Animales , Evolución Molecular , Variación Genética/genética , Receptores de Superficie Celular/genética , Receptores de Superficie Celular/metabolismo , Receptores Nicotínicos/genética , Receptores Nicotínicos/metabolismo , Venenos de Serpiente/metabolismo , Serpientes/genética
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