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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Gene
Article . 2000 . Peer-reviewed
License: Elsevier TDM
Data sources: Crossref
Gene
Article . 2000
versions View all 2 versions

Ermap, a gene coding for a novel erythroid specific adhesion/receptor membrane protein

Authors: Ye, TZ; Gordon, CT; Lai, YH; Fujiwara, Y; Peters, LL; Perkins, AC; Chui, DHK;

Ermap, a gene coding for a novel erythroid specific adhesion/receptor membrane protein

Abstract

Ermap (erythroid membrane-associated protein), a gene coding for a novel transmembrane protein produced exclusively in erythroid cells, is described. It is mapped to murine Chromosome 4, 57 cM distal to the centromere. The initial cDNA clone was isolated from a day 9 murine embryonic erythroid cell cDNA library. The predicted peptide sequence suggests that ERMAP is a transmembrane protein with two extracellular immunoglobulin folds, as well as a highly conserved B30.2 domain and several phosphorylation consensus sequences in the cytoplasmic region. ERMAP shares a high homology throughout the entire peptide with butyrophilin, a glycoprotein essential for milk lipid droplet formation and release. A GFP-ERMAP fusion protein was localized to the plasma membrane and cytoplasmic vesicles in transiently transfected 293T cells. Northern blot analysis and in-situ hybridization demonstrated that Ermap expression was restricted to fetal and adult erythroid tissues. ERMAP is likely a novel adhesion/receptor molecule specific for erythroid cells.

Keywords

Male, Cytoplasm, Luminescent-Proteins, Erythrocytes, Mouse, Transcription Factor, Blotting-Northern, Immunoglobulin Superfamily, In-Situ-Hybridization, Gene-Expression-Regulation-Developmental, Major Histocompatibility Complex, Mice, Tissue-Distribution, SUPPORT-U-S-GOVT-P-H-S, Membrane-Proteins, Butyrophilin, Cloning, Molecular, In Situ Hybridization, Chromosome Mapping, Gene Expression Regulation, Developmental, Sequence-Homology-Amino-Acid, Fat Globule-Membrane, Cell-Line, Cloning-Molecular, Embryo, Blood Group Antigens, K562-Cells, Sequence-Analysis-DNA, Cell-Adhesion-Molecules, Gene-Expression-Regulation, DNA-Complementary, Human, Cell-Adhesion, 570, DNA, Complementary, Green Fluorescent Proteins, Recombinant-Fusion-Proteins, 610, Sequence-Alignment, Cell Line, Sequence, Cell Adhesion, Animals, Humans, Amino Acid Sequence, Cell-Nucleus, SUPPORT-NON-U-S-GOVT, Cell Nucleus, Molecular-Sequence-Data, Butyrophilins, Animal, Macrophages, Mice-Inbred-C57BL, Blotting, Northern, Embryo, Mammalian, Muridae, Gene Expression Regulation, Chromosome-Mapping, RNA, Mammary Epithelial-Cells, Glycoprotein, Cell Adhesion Molecules

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Powered by OpenAIRE graph
citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
29
Average
Top 10%
Top 10%