Literature DB >> 8183555

The Eck receptor tyrosine kinase is implicated in pattern formation during gastrulation, hindbrain segmentation and limb development.

P Ganju1, K Shigemoto, J Brennan, A Entwistle, A D Reith.   

Abstract

Members of the protein superfamily of transmembrane receptor tyrosine kinases are key components of intercellular signal transduction pathways that elicit appropriate cellular responses to environmental cues during development of multicellular organisms. In a search for additional receptor tyrosine kinases expressed during mouse embryogenesis we cloned the murine homolog of Eck, a member of the Eph subfamily, that maps to the distal region of mouse chromosome 4. Specific antisera defined Eck in murine embryonic cells as a glycoprotein of 130 kDa with an intrinsic autophosphorylation activity. Immunohistochemical staining and laser scanning microscopy revealed a dynamic and tightly regulated distribution of Eck receptor protein in the developing mouse embryo. During gastrulation, a high transient distribution of Eck was seen in mesodermal cells aggregating in the midline as notochordal plate. A similar restriction of Eck receptor protein was apparent along the rostrocaudal axis of the developing neural tube. In hindbrain neuroepithelia, Eck protein localised specifically to cells of rhombomere 4 and was also seen transiently in cells populating second and third branchial arches and neurogenic facial crest VII-VIII and IX-X. Receptor distribution also implicated Eck in development of the proximodistal axis of the limb, expression being restricted to distal regions of limb bud mesenchyme. At later stages, additional sites of Eck protein expression were seen in the cartilaginous model of the skeleton, tooth primordia, infundibular component of the pituitary and various fetal tissue epithelia. Taken together, our data suggest pleiotropic functions for the Eck receptor, initially in distinctive aspects of pattern formation and subsequently in development of several fetal tissues, and reveal possible allelism with known mouse developmental mutant loci.

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Year:  1994        PMID: 8183555

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  18 in total

Review 1.  Differential regulation of EphA2 in normal and malignant cells.

Authors:  Jennifer Walker-Daniels; Angela R Hess; Mary J C Hendrix; Michael S Kinch
Journal:  Am J Pathol       Date:  2003-04       Impact factor: 4.307

2.  Developmental expression of Eph and ephrin family genes in mammalian small intestine.

Authors:  Shabana Islam; Anthony M Loizides; John J Fialkovich; Richard J Grand; Robert K Montgomery
Journal:  Dig Dis Sci       Date:  2010-01-29       Impact factor: 3.199

Review 3.  Therapeutic targeting of EPH receptors and their ligands.

Authors:  Andrew W Boyd; Perry F Bartlett; Martin Lackmann
Journal:  Nat Rev Drug Discov       Date:  2014-01       Impact factor: 84.694

4.  Purification of a ligand for the EPH-like receptor HEK using a biosensor-based affinity detection approach.

Authors:  M Lackmann; T Bucci; R J Mann; L A Kravets; E Viney; F Smith; R L Moritz; W Carter; R J Simpson; N A Nicola; K Mackwell; E C Nice; A F Wilks; A W Boyd
Journal:  Proc Natl Acad Sci U S A       Date:  1996-03-19       Impact factor: 11.205

5.  Shared and distinct functions of RAGS and ELF-1 in guiding retinal axons.

Authors:  B Monschau; C Kremoser; K Ohta; H Tanaka; T Kaneko; T Yamada; C Handwerker; M R Hornberger; J Löschinger; E B Pasquale; D A Siever; M F Verderame; B K Müller; F Bonhoeffer; U Drescher
Journal:  EMBO J       Date:  1997-03-17       Impact factor: 11.598

6.  Fibroblast growth factor receptor-mediated rescue of x-ephrin B1-induced cell dissociation in Xenopus embryos.

Authors:  L D Chong; E K Park; E Latimer; R Friesel; I O Daar
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

7.  gdt1, a new signal transduction component for negative regulation of the growth-differentiation transition in Dictyostelium discoideum.

Authors:  C Zeng; C Anjard; K Riemann; A Konzok; W Nellen
Journal:  Mol Biol Cell       Date:  2000-05       Impact factor: 4.138

8.  EphA2 immunoconjugate as molecularly targeted chemotherapy for ovarian carcinoma.

Authors:  Jeong-Won Lee; Hee Dong Han; Mian M K Shahzad; Seung Wook Kim; Lingegowda S Mangala; Alpa M Nick; Chunhua Lu; Robert R Langley; Rosemarie Schmandt; Hye-Sun Kim; Shenlan Mao; John Gooya; Christine Fazenbaker; Dowdy Jackson; David A Tice; Charles N Landen; Robert L Coleman; Anil K Sood
Journal:  J Natl Cancer Inst       Date:  2009-07-29       Impact factor: 13.506

9.  Embryonic stem cells express multiple Eph-subfamily receptor tyrosine kinases.

Authors:  J D Lickliter; F M Smith; J E Olsson; K L Mackwell; A W Boyd
Journal:  Proc Natl Acad Sci U S A       Date:  1996-01-09       Impact factor: 11.205

10.  ELF-2, a new member of the Eph ligand family, is segmentally expressed in mouse embryos in the region of the hindbrain and newly forming somites.

Authors:  A D Bergemann; H J Cheng; R Brambilla; R Klein; J G Flanagan
Journal:  Mol Cell Biol       Date:  1995-09       Impact factor: 4.272

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