Center for Molecular Biology of Heidelberg University (ZMBH), DKFZ-ZMBH Alliance, D-69120 Heidelberg, Germany.
Hopp Children's Cancer Center (KiTZ) Heidelberg, Division of Pediatric Neurooncology, German Cancer Consortium (DKTK), and German Cancer Research Center (DKFZ), D-69120 Heidelberg, Germany.
Science. 2021 Aug 27;373(6558). doi: 10.1126/science.abg4696. Epub 2021 Jul 29.
Organ development is orchestrated by cell- and time-specific gene regulatory networks. In this study, we investigated the regulatory basis of mouse cerebellum development from early neurogenesis to adulthood. By acquiring snATAC-seq (single-nucleus assay for transposase accessible chromatin using sequencing) profiles for ~90,000 cells spanning 11 stages, we mapped cerebellar cell types and identified candidate cisregulatory elements (CREs). We detected extensive spatiotemporal heterogeneity among progenitor cells and a gradual divergence in the regulatory programs of cerebellar neurons during differentiation. Comparisons to vertebrate genomes and snATAC-seq profiles for ∼20,000 cerebellar cells from the marsupial opossum revealed a shared decrease in CRE conservation during development and differentiation as well as differences in constraint between cell types. Our work delineates the developmental and evolutionary dynamics of gene regulation in cerebellar cells and provides insights into mammalian organ development.
器官发育是由细胞和时间特异性的基因调控网络协调的。在这项研究中,我们研究了从小鼠神经发生到成年期的小脑发育的调控基础。通过对跨越 11 个阶段的约 90,000 个细胞进行 snATAC-seq(使用测序的转座酶可及染色质的单细胞分析)分析,我们绘制了小脑细胞类型并鉴定了候选顺式调控元件(CREs)。我们在祖细胞中检测到广泛的时空异质性,并在分化过程中发现小脑神经元的调控程序逐渐分歧。与脊椎动物基因组和来自有袋动物负鼠的约 20,000 个小脑细胞的 snATAC-seq 图谱进行比较,揭示了在发育和分化过程中 CRE 保守性的共同下降,以及细胞类型之间的约束差异。我们的工作描绘了小脑细胞中基因调控的发育和进化动态,并为哺乳动物器官发育提供了新的见解。