Single-Cell RNA-Seq Reveals Lineage and X Chromosome Dynamics in Human Preimplantation Embryos

single cell sequencing;SNS;单细胞测序;单细胞多组学
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Sophie Petropoulos, Daniel Edsgärd, Björn Reinius, Qiaolin Deng, Sarita Pauliina Panula, Simone Codeluppi, Alvaro Plaza Reyes, Sten Linnarsson, Rickard Sandberg, Fredrik Lanner

  • Cell
  • 2016
  • 66.85
  • 165(4):1012-26.
  • Human
  • 单细胞测序
  • Trophectoderm cell
  • 技术分享
  • 其它细胞
  • ABCG2, ACTN1, ADA15, ADK, PPB1, ANKR6, ANXA6, RHG23, ARHGQ, VPP4, VATB1, AT8B1, BASP1, C4BPB, ICAL, CD24, CD53, CITE4, CLD10, CLD3, CLD4, CP26A, DAB2, AUXI, EFNA1, ELOV6, EMP2, AMPE, FABPH, RFLB, FAS, FXL18, FHL2, FOLR1, FRM4B, GAB2, GLT10, GATA2, GATA3, GAPR1, SAP3, RAI3, GRB1L, GRHL2, LARG2, HIP1, IFT25, JDP2, K1C18, K1C19, K2C8, LAD1, LRP2, LRRF1, MYC, MYCT1, MLRS, MYO6, MYOF, NIM1, NPC2, OLFL1, OSBL6, PALLD, PDGFA, PDLI1, PI51B, PLAC8, PPME1, PPT1, PRSS8, PTGES, PWP2B, RAB25, S10AG, S10A6, SH3G3, S12A3, S19A3, S28A3, NPT2B, CTR2, CTR4, LAT1, SUN3, SYBU, TACD2, TAGL2, TF7L1, TEAD1, TET2, TFR1, TGBR3, T106C, TM171, TMPSD, TMPS2, TSN15, VAMP8, WNT7A
  • UBERON_0000922

Abstract

Mouse studies have been instrumental in forming our current understanding of early cell-lineage decisions; however, similar insights into the early human development are severely limited. Here, we present a comprehensive transcriptional map of human embryo development, including the sequenced transcriptomes of 1,529 individual cells from 88 human preimplantation embryos. These data show that cells undergo an intermediate state of co-expression of lineage-specific genes, followed by a concurrent establishment of the trophectoderm, epiblast, and primitive endoderm lineages, which coincide with blastocyst formation. Female cells of all three lineages achieve dosage compensation of X chromosome RNA levels prior to implantation. However, in contrast to the mouse, XIST is transcribed from both alleles throughout the progression of this expression dampening, and X chromosome genes maintain biallelic expression while dosage compensation proceeds. We envision broad utility of this transcriptional atlas in future studies on human development as well as in stem cell research.
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