Spatiotemporal transcriptomic maps of whole mouse embryos at the onset of organogenesis.
Spatiotemporal transcriptomic maps of whole mouse embryos at the onset of organogenesis.
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在器官发生时,整个小鼠胚胎的时空转录组图。
DOI:
10.1038/s41588-023-01435-6
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发表时间:
2023-07
期刊:
影响因子:
30.8
通讯作者:
Meissner, Alexander
中科院分区:
文献类型:
--
作者:
Kumar, Abhishek Sampath;Tian, Luyi;Bolondi, Adriano;Hernandez, Amelia Aragones;Stickels, Robert;Kretzmer, Helene;Murray, Evan;Wittler, Lars;Walther, Maria;Barakat, Gabriel;Haut, Leah;Elkabetz, Yechiel;Macosko, Evan Z.;Guignard, Leo;Chen, Fei;Meissner, Alexander
Spatiotemporal orchestration of gene expression is required for proper embryonic development. The use of single-cell technologies has begun to provide improved resolution of early regulatory dynamics, including detailed molecular definitions of most cell states during mouse embryogenesis. Here we used Slide-seq to build spatial transcriptomic maps of complete embryonic day (E) 8.5 and E9.0, and partial E9.5 embryos. To support their utility, we developed sc3D, a tool for reconstructing and exploring three-dimensional ‘virtual embryos’, which enables the quantitative investigation of regionalized gene expression patterns. Our measurements along the main embryonic axes of the developing neural tube revealed several previously unannotated genes with distinct spatial patterns. We also characterized the conflicting transcriptional identity of ‘ectopic’ neural tubes that emerge in Tbx6 mutant embryos. Taken together, we present an experimental and computational framework for the spatiotemporal investigation of whole embryonic structures and mutant phenotypes. Slide-seq profiling of mouse embryos at the onset of organogenesis (embryonic days 8.5–9.5) coupled with a new three-dimensional reconstruction and visualization tool (sc3D) provides high-resolution maps of spatiotemporal gene expression dynamics.
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影响因子:
64.8
作者:
Cao, Junyue;Spielmann, Malte;Shendure, Jay
通讯作者:
Shendure, Jay
影响因子:
4.6
作者:
Delile, Julien;Rayon, Teresa;Sagner, Andreas
通讯作者:
Sagner, Andreas
影响因子:
2.7
作者:
Chapman, DL;Agulnik, I;Papaioannou, VE
通讯作者:
Papaioannou, VE
影响因子:
64.8
作者:
Dickinson ME;Flenniken AM;Ji X;Teboul L;Wong MD;White JK;Meehan TF;Weninger WJ;Westerberg H;Adissu H;Baker CN;Bower L;Brown JM;Caddle LB;Chiani F;Clary D;Cleak J;Daly MJ;Denegre JM;Doe B;Dolan ME;Edie SM;Fuchs H;Gailus-Durner V;Galli A;Gambadoro A;Gallegos J;Guo S;Horner NR;Hsu CW;Johnson SJ;Kalaga S;Keith LC;Lanoue L;Lawson TN;Lek M;Mark M;Marschall S;Mason J;McElwee ML;Newbigging S;Nutter LM;Peterson KA;Ramirez-Solis R;Rowland DJ;Ryder E;Samocha KE;Seavitt JR;Selloum M;Szoke-Kovacs Z;Tamura M;Trainor AG;Tudose I;Wakana S;Warren J;Wendling O;West DB;Wong L;Yoshiki A;International Mouse Phenotyping Consortium;Jackson Laboratory;Infrastructure Nationale PHENOMIN, Institut Clinique de la Souris (ICS);Charles River Laboratories;MRC Harwell;Toronto Centre for Phenogenomics;Wellcome Trust Sanger Institute;RIKEN BioResource Center;MacArthur DG;Tocchini-Valentini GP;Gao X;Flicek P;Bradley A;Skarnes WC;Justice MJ;Parkinson HE;Moore M;Wells S;Braun RE;Svenson KL;de Angelis MH;Herault Y;Mohun T;Mallon AM;Henkelman RM;Brown SD;Adams DJ;Lloyd KC;McKerlie C;Beaudet AL;Bućan M;Murray SA
通讯作者:
Murray SA
影响因子:
2.6
作者:
Chapman, DL;Cooper-Morgan, A;Papaioannou, VE
通讯作者:
Papaioannou, VE