PUBLICATION

The translocon-associated protein b (TRAPb) in zebrafish embryogenesis. I. Enhanced expression of transcripts in notochord and hatching gland precursors

Authors
Mangos, S., Krawetz, R., and Kelly, G.M.
ID
ZDB-PUB-010102-3
Date
2000
Source
Molecular and cellular biochemistry   215(1-2): 93-101 (Journal)
Registered Authors
Kelly, Greg, Krawetz, Roman, Mangos, Steve
Keywords
endoplasmic reticulum; protein targeting; zebrafish (Danio); embryogenesis; notochord; polster
MeSH Terms
  • Nuclear Proteins/metabolism
  • Time Factors
  • RNA, Messenger/metabolism
  • Open Reading Frames
  • Embryo, Nonmammalian/metabolism*
  • Embryo, Nonmammalian/physiology
  • DNA, Complementary/metabolism
  • Molecular Sequence Data
  • Receptors, Peptide/biosynthesis*
  • Zebrafish/embryology*
  • Chickens
  • Chromosome Mapping
  • Calcium-Binding Proteins/biosynthesis*
  • ran GTP-Binding Protein/metabolism
  • Gastrula/metabolism
  • Receptors, Cytoplasmic and Nuclear/biosynthesis*
  • Blastocyst/metabolism
  • Membrane Glycoproteins*
  • Endoplasmic Reticulum/metabolism
  • Amino Acid Sequence
  • Nucleic Acid Hybridization
  • Base Sequence
  • Humans
  • Animals
  • Reverse Transcriptase Polymerase Chain Reaction
  • Notochord/metabolism*
  • In Situ Hybridization
  • Two-Hybrid System Techniques
  • Radiation Hybrid Mapping
PubMed
11204460 Full text @ Mol. Cell. Biochem.
Abstract
The normal translocation of nascent polypeptides into the lumen of the endoplasmic reticulum (ER) is thought to be aided in part by a translocon-associated protein (TRAP) complex consisting of 4 protein subunits. The association of mature proteins with the ER and Golgi, or other intracellular locales, such as lysosomes, depends on the initial targeting of the nascent polypeptide to the ER membrane. A similar scenario must also exist for proteins destined for secretion. We have identified a member of the TRAP complex using a two hybrid screen to isolate proteins that bind to zebrafish (Danio) Ran binding protein 1. The polypeptide predicted from the largest open reading frame contains 183 amino acids with a 86 and 87% sequence identity to the TRAPbeta subunits in human and chicken, respectively. Sequence analysis identified a cleavable amino-terminal signal peptide in the zebrafish TRAPbeta subunit and a region of the protein spans the membrane of the endoplasmic reticulum. A reverse transcriptase-polymerase chain reaction assay showed that TRAPbeta mRNA is expressed in the developing zebrafish embryo. TRAPbeta mRNA is maternally supplied to the egg and is expressed constitutively throughout development and in the adult. This pattern of expression indicates that the message encoding part of the machinery targeting nascent polypeptides to the ER lumen is available at the onset of embryogenesis when the rate of translation increases exponentially over that occurring in the oocyte. In situ hybridization was used to test whether or not TRAPbeta transcripts might become localized and/or enriched in the developing embryo. Homogeneous staining is seen in the blastula and early gastrula stages. At mid-to-late gastrula stages, however, the message becomes enriched in the developing notochord and polster, or hatching gland rudiment. The TRAPbeta gene, mapped using the LN54 mouse-zebrafish radiation hybrid panel to linkage group 19, resides next to a gene (Z15451) which has sequence homology to notch2 and vascular endothelial growth factor. TRAPbeta, however, does not appear to belong to a group of genes which are syntenic with orthologues or paralogues on human chromosomes.
Genes / Markers
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Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping