Clonally heritable gene expression imparts a layer of diversity within cell types.

Cell systems Pub Date : 2024-02-21 Epub Date: 2024-02-09 DOI:10.1016/j.cels.2024.01.004
Jeff E Mold, Martin H Weissman, Michael Ratz, Michael Hagemann-Jensen, Joanna Hård, Carl-Johan Eriksson, Hosein Toosi, Joseph Berghenstråhle, Christoph Ziegenhain, Leonie von Berlin, Marcel Martin, Kim Blom, Jens Lagergren, Joakim Lundeberg, Rickard Sandberg, Jakob Michaëlsson, Jonas Frisén
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Abstract

Cell types can be classified according to shared patterns of transcription. Non-genetic variability among individual cells of the same type has been ascribed to stochastic transcriptional bursting and transient cell states. Using high-coverage single-cell RNA profiling, we asked whether long-term, heritable differences in gene expression can impart diversity within cells of the same type. Studying clonal human lymphocytes and mouse brain cells, we uncovered a vast diversity of heritable gene expression patterns among different clones of cells of the same type in vivo. We combined chromatin accessibility and RNA profiling on different lymphocyte clones to reveal thousands of regulatory regions exhibiting interclonal variation, which could be directly linked to interclonal variation in gene expression. Our findings identify a source of cellular diversity, which may have important implications for how cellular populations are shaped by selective processes in development, aging, and disease. A record of this paper's transparent peer review process is included in the supplemental information.

克隆遗传的基因表达为细胞类型提供了一层多样性。
细胞类型可根据共同的转录模式进行分类。同一类型的单个细胞之间的非遗传变异被归因于随机转录突变和瞬时细胞状态。利用高覆盖率的单细胞 RNA 图谱,我们提出了一个问题:基因表达的长期遗传差异是否会在同一类型的细胞中产生多样性。通过对克隆人类淋巴细胞和小鼠脑细胞的研究,我们发现了体内同一类型细胞的不同克隆间遗传基因表达模式的巨大多样性。我们将不同淋巴细胞克隆的染色质可及性和 RNA 分析结合起来,发现了数千个表现出克隆间差异的调控区域,这些区域可能与基因表达的克隆间差异直接相关。我们的研究发现了细胞多样性的来源,这可能对细胞群在发育、衰老和疾病过程中如何通过选择性过程形成具有重要意义。补充信息中包含了本文透明的同行评审过程记录。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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