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Clonal hematopoiesis sees Twin Peaks

机译:克隆造血会看到双峰

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摘要

Clonal hematopoiesis (CH) is a fundamental process in the aging of the blood system; however, it remains enigmatic why some individuals of the same age carry mutations, whereas others do not or carry different mutations with different variant allele frequencies (VAF). In this issue of Blood, Fabre et al(1) and Hansen et al(2) address the differential roles of nature (genotype/heritability) vs nurture (environment) in the evolution of age-related clonal hematopoiesis (ARCH).(3) In these studies, twin concordance analysis was used to determine the germline contribution to ARCH.(4) In both studies, no hereditary component of ARCH could be detected. Therefore, it is most likely that the variability of ARCH in the population can be explained by differential environmental exposures. Although such a conclusion is reasonable, a few specific aspects of the nature vs nurture dilemma in CH need to be considered.
机译:克隆造血(CH)是血液系统老化的基本过程; 然而,它仍然是为什么同一年龄的某些人具有突变的某些人,而其他人则没有或携带不同的变异等位基因频率(VAF)的不同突变。 在这个问题上,Fabre等(1)和Hansen等人(2)地解决了性质(基因型/遗传性)对年龄相关克隆血液血液(拱门)的演变中的差异性(基因型/遗传性)与培育(环境)。(3 )在这些研究中,用于确定对拱的种系贡献。(4)在这两项研究中,可以检测到拱门的任何遗传部件。 因此,最有可能通过差异环境暴露来解释群体中拱的可变性。 虽然这样的结论是合理的,但需要考虑少数特定方面对CH中的侵犯困境。

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