Literature DB >> 9384382

Binary specification of the embryonic lineage in Caenorhabditis elegans.

T Kaletta1, H Schnabel, R Schnabel.   

Abstract

In Caenorhabditis elegans, the early embryo contains five somatic founder cells (known as AB, MS, E, C and D) which give rise to very different lineages. Two simply produce twenty intestinal (E) or muscle (D) cells each, whereas the remainder produce a total of 518 cells which collectively contribute in a complex pattern to a variety of tissues. A central problem in embryonic development is to understand how the developmental potential of blastomeres is restricted to permit the terminal expression of such complex differentiation patterns. Here we identify a gene, lit-1, that appears to play a central role in controlling the asymmetry of cell division during embryogenesis in C. elegans. Mutants in lit-1 suggest that its product controls up to six consecutive binary switches which cause one of the two equivalent cells produced at each cleavage to assume a posterior fate. Most blastomere identities in C. elegans may therefore stem from a process of stepwise binary diversification.

Entities:  

Mesh:

Year:  1997        PMID: 9384382     DOI: 10.1038/36869

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  63 in total

Review 1.  Lineage programming: navigating through transient regulatory states via binary decisions.

Authors:  Vincent Bertrand; Oliver Hobert
Journal:  Curr Opin Genet Dev       Date:  2010-05-27       Impact factor: 5.578

2.  Mass spectrometric comparison of N-glycan profiles from Caenorhabditis elegans mutant embryos.

Authors:  Hildegard Geyer; Martin Schmidt; Matthias Müller; Ralf Schnabel; Rudolf Geyer
Journal:  Glycoconj J       Date:  2012-03-10       Impact factor: 2.916

3.  Tracking and Quantifying Developmental Processes in C. elegans Using Open-source Tools.

Authors:  Priyanka Dutta; Christina Lehmann; Devang Odedra; Deepika Singh; Christian Pohl
Journal:  J Vis Exp       Date:  2015-12-16       Impact factor: 1.355

Review 4.  Wnt Signaling Polarizes C. elegans Asymmetric Cell Divisions During Development.

Authors:  Arielle Koonyee Lam; Bryan T Phillips
Journal:  Results Probl Cell Differ       Date:  2017

5.  Phosphorylation of TCF proteins by homeodomain-interacting protein kinase 2.

Authors:  Hiroki Hikasa; Sergei Y Sokol
Journal:  J Biol Chem       Date:  2011-02-01       Impact factor: 5.157

6.  Nemo is required in a subset of photoreceptors to regulate the speed of ommatidial rotation.

Authors:  Ryan W Fiehler; Tanya Wolff
Journal:  Dev Biol       Date:  2007-10-30       Impact factor: 3.582

7.  Wnt signaling drives WRM-1/beta-catenin asymmetries in early C. elegans embryos.

Authors:  Kuniaki Nakamura; Soyoung Kim; Takao Ishidate; Yanxia Bei; Kaming Pang; Masaki Shirayama; Chris Trzepacz; Daniel R Brownell; Craig C Mello
Journal:  Genes Dev       Date:  2005-08-01       Impact factor: 11.361

8.  Asymmetric cortical and nuclear localizations of WRM-1/beta-catenin during asymmetric cell division in C. elegans.

Authors:  Hisako Takeshita; Hitoshi Sawa
Journal:  Genes Dev       Date:  2005-08-01       Impact factor: 11.361

9.  The N- or C-terminal domains of DSH-2 can activate the C. elegans Wnt/beta-catenin asymmetry pathway.

Authors:  Ryan S King; Stephanie L Maiden; Nancy C Hawkins; Ambrose R Kidd; Judith Kimble; Jeff Hardin; Timothy D Walston
Journal:  Dev Biol       Date:  2009-01-23       Impact factor: 3.582

10.  Loss of SEC-23 in Caenorhabditis elegans causes defects in oogenesis, morphogenesis, and extracellular matrix secretion.

Authors:  Brett Roberts; Caroline Clucas; Iain L Johnstone
Journal:  Mol Biol Cell       Date:  2003-08-07       Impact factor: 4.138

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.