TY - JOUR
T1 - Single-cell nuclear architecture across cell types in the mouse brain
AU - Takei, Yodai
AU - Zheng, Shiwei
AU - Yun, Jina
AU - Shah, Sheel
AU - Pierson, Nico
AU - White, Jonathan
AU - Schindler, Simone
AU - Tischbirek, Carsten H.
AU - Yuan, Guo Cheng
AU - Cai, Long
N1 - Publisher Copyright:
Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works
PY - 2021/10/29
Y1 - 2021/10/29
N2 - Diverse cell types in tissues have distinct gene expression programs, chromatin states, and nuclear architectures. To correlate such multimodal information across thousands of single cells in mouse brain tissue sections, we use integrated spatial genomics, imaging thousands of genomic loci along with RNAs and epigenetic markers simultaneously in individual cells. We reveal that cell type-specific association and scaffolding of DNA loci around nuclear bodies organize the nuclear architecture and correlate with differential expression levels in different cell types. At the submegabase level, active and inactive X chromosomes access similar domain structures in single cells despite distinct epigenetic and expression states. This work represents a major step forward in linking single-cell three-dimensional nuclear architecture, gene expression, and epigenetic modifications in a native tissue context.
AB - Diverse cell types in tissues have distinct gene expression programs, chromatin states, and nuclear architectures. To correlate such multimodal information across thousands of single cells in mouse brain tissue sections, we use integrated spatial genomics, imaging thousands of genomic loci along with RNAs and epigenetic markers simultaneously in individual cells. We reveal that cell type-specific association and scaffolding of DNA loci around nuclear bodies organize the nuclear architecture and correlate with differential expression levels in different cell types. At the submegabase level, active and inactive X chromosomes access similar domain structures in single cells despite distinct epigenetic and expression states. This work represents a major step forward in linking single-cell three-dimensional nuclear architecture, gene expression, and epigenetic modifications in a native tissue context.
UR - http://www.scopus.com/inward/record.url?scp=85118406401&partnerID=8YFLogxK
U2 - 10.1126/science.abj1966
DO - 10.1126/science.abj1966
M3 - Article
C2 - 34591592
AN - SCOPUS:85118406401
SN - 0036-8075
VL - 374
SP - 586
EP - 594
JO - Science
JF - Science
IS - 6567
ER -