Collapse of embryonic identities and emergence of functional diversity during motor neuron maturation.

IF 7.7 1区 生物学 Q1 CELL BIOLOGY
Cell reports Pub Date : 2026-10-27 Epub Date: 2026-09-30 DOI:10.1016/j.celrep.2026.118062
Yijia Chen, Hsuan-Ming Chi, Aileen Tian, Courtney Stains, Alison Miller, Tulsi Patel
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引用次数: 0

Abstract

Post-mitotic neurons undergo a protracted maturation period as they extend axons to their targets, form synapses, and refine electrophysiological properties. We use temporal single-nucleus multiome sequencing to map molecular underpinnings of maturation in mouse skeletal motor neurons (SMNs). Our data show that SMNs undergo transcriptional changes as they mature, but more strikingly, we find that diversity within SMNs changes dramatically as they transition from axon targeting to forming functional circuits. Embryonic SMNs comprise dozens of transcriptional subclusters representing known motor columns and pools, which utilize specific transcriptional programs to innervate unique muscle targets. However, this transcriptional diversity is largely lost by early postnatal life, and SMNs re-diversify into adult alpha, gamma, and type3 identities, which innervate different fibers within each muscle to regulate movement. This work shows that transcriptional subtype diversity within a neuron type, and the underlying regulatory programs, can transform completely during maturation to accommodate changing functional needs.

运动神经元成熟过程中胚胎身份的瓦解和功能多样性的出现。
有丝分裂后的神经元经历了一个漫长的成熟期,因为它们将轴突延伸到它们的目标,形成突触,并完善电生理特性。我们使用时间单核多组测序来绘制小鼠骨骼运动神经元(SMNs)成熟的分子基础。我们的数据表明,随着smn的成熟,它们会发生转录变化,但更引人注目的是,我们发现smn内的多样性在它们从轴突靶向转变为形成功能回路时发生了巨大变化。胚胎smn包括数十个转录亚簇,代表已知的运动柱和池,它们利用特定的转录程序来支配独特的肌肉目标。然而,这种转录多样性在出生后的早期生活中很大程度上消失了,并且smn重新分化为成年α, γ和3型身份,它们支配每块肌肉内的不同纤维来调节运动。这项工作表明,神经元类型中的转录亚型多样性和潜在的调控程序可以在成熟过程中完全转变,以适应不断变化的功能需求。
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来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
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