A DNA Typewriter records the cell lineage history of a mouse, from zygote to late organogenesis.

Qi Yu, Haedong Kim, Sophie Seidel, James F Acosta-Clark, Beth K Martin, Kyle O'Connor, Riza M Daza, Molly Gasperini, Jenny F Nathans, Maggie Lam, Elena Gamo, Shruthi VijayKumar, Lauren Kuo, Jean-Benoît Lalanne, Kamen P Simeonov, Marion Pepper, Cole Trapnell, Jesse M Gray, Junhong Choi, Chengxiang Qiu, Jay Shendure
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Abstract

Mammalian biology unfolds over time, within tissues and organs opaque to our eyes and instruments. We applied DNA Typewriter, a sequential molecular recorder, to record the cell lineage of a mouse over nearly two weeks of development. From one embryo, we reconstruct a time-calibrated, parsimony-supported, zygote-rooted phylogeny of 1.28M transcriptionally-profiled cells. A burst of editing unequivocally marks the daughters of the first cleavage, which serve as inline replicates. We quantify clonal dominance arising during gastrulation. Tree siblings share cell type far above chance; heterotypic siblings mark terminal differentiations. Temporal sweeps of clade co-occurrence recover a dated hierarchy of cell-type couplings; imputed labels for internal nodes recapitulate known state paths. A lineage-anchored ontogeny of mammalian development, long out of reach, is coming into view.

具有DNA打字机的发育小鼠的细胞谱系历史的体内重建,从受精卵到器官发生晚期。
四十多年前绘制的秀丽隐杆线虫的完整细胞谱系是可处理的,因为这种动物很小,透明,并且谱系不变。大多数动物都不是这些动物,它们的细胞要多几个数量级,不透明,而且发育具有很大的随机性。自2016年以来,基于基因组编辑的谱系追踪为这类生物的密集细胞谱系重建打开了大门,但事实证明,实现这一承诺在技术上具有挑战性。在这里,我们应用DNA打字机9-11,一种基于初始编辑的记录器,按照严格的顺序将随机符号插入写入工程基因组磁带,以追踪小鼠从受精卵(E0)到晚期器官发生(E13.5)的发育。我们通过原核注射(PNI)将编码引物编辑器、工程化引物编辑引导RNA (epegRNAs)和pol - iii驱动的环状带RNA (circTAPE)的构建物引入野生型受精卵,然后通过单核转录分析(sci-RNA-seq3) 12和配对环状带恢复对胚胎进行分析。从一个E13.5胚胎中,我们恢复了约1.75M个单核转录组,并重建了1,340,794个带有简约性节点支持的注释细胞的时间校准系统发育。第一次细胞分裂是明确的,尽管产生的卵裂球对胚胎本身的贡献是不对称的,但它们是命运中性的,并作为内部复制来复制每一个发现。一个适度的原肠形成前的奠基者群体在胚胎中占主导地位,在奠基者分配的一到两个细胞周期内,不平等超过中性预期,但这些奠基者仍然广泛地具有多能性;在器官发生过程中,在特定谱系中出现克隆优势的第二阶段。在最精细的尺度上,兄弟姐妹细胞共享细胞类型的几率超过9倍,在空间受限的创始人池中产生的细胞类型达到68- 107倍,而在末端分支的异型结构中,器官发生的最新分化是清晰可见的。仅从进化枝共现,我们就恢复了从E8.5开始的细菌层组织和具有分支点的细胞型偶联的过时的层次结构。最后,通过将这些数据与我们的小鼠单细胞发育时间序列相结合13,我们推断了大多数内部节点的转录状态和注释,并恢复了不同细胞类型的已建立的状态历史。所有数据都是免费提供的,连同NextCell,一个交互式浏览器,用于注释小鼠从受精卵到晚期器官发生发育的细胞系统发育。
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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