Literature DB >> 1907207

Molecular biology of the Rh antigens.

P Agre1, J P Cartron.   

Abstract

The RBC Rh antigens are of large clinical importance, but until recently have been poorly understood at a molecular level. The Rh polypeptides are a family of nonglycosylated Mr 30- to 32-Kd transmembrane proteins that are core structural components of the Rh antigens and have been purified and partially characterized biochemically. Rh polypeptides are present in RBCs from normal humans and other mammalian species and are probably required for normal membrane integrity, because they appear to be missing from the RBCs of the rare Rhnull individuals that express several membrane defects. The Rh polypeptides contain an exofacial free sulfhydryl that is important for Rh antigenic reactivity and several intracellular sulfhydryls that appear to be palmitylated, but most of the molecule appears to reside between the leaflets of the phospholipid bilayer. The cDNA coding for a 416-amino acid Rh polypeptide was recently isolated but was not found to share sequence homology with any known protein, and Northern analysis indicated that Rh is erythroid specific. The Rh antigens within the native membranes are thought to exist as a complex of Rh polypeptides and multiple other membrane components, including certain Rh-related glycoproteins. While it is thought that this assembly may be important for the Rh antigenic reactivity, the structural basis of this remains to be established. While the physiologic role of Rh is yet to be defined, several clues indicate that it may play a role in the organization of membrane phospholipids or synthesis or membrane expression of various glycoproteins. While our knowledge of Rh is still very incomplete, recent research has significantly advanced the molecular understanding of these important blood group antigens.

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Year:  1991        PMID: 1907207

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  19 in total

1.  Germline variable region gene segment derivation of human monoclonal anti-Rh(D) antibodies. Evidence for affinity maturation by somatic hypermutation and repertoire shift.

Authors:  J M Bye; C Carter; Y Cui; B D Gorick; S Songsivilai; G Winter; N C Hughes-Jones; J D Marks
Journal:  J Clin Invest       Date:  1992-12       Impact factor: 14.808

2.  Genetic recombination at the human RH locus: a family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE gene.

Authors:  C H Huang; Y Chen; M Reid; S Ghosh
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

3.  Characterization of the recombination hot spot involved in the genomic rearrangement leading to the hybrid D-CE-D gene in the D(VI) phenotype.

Authors:  G Matassi; B Chérif-Zahar; I Mouro; J P Cartron
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

4.  CD144+ endothelial microparticles as a marker of endothelial injury in neonatal ABO blood group incompatibility.

Authors:  Hisham A E Awad; Azza A G Tantawy; Rania A El-Farrash; Eman A Ismail; Noha M Youssif
Journal:  Blood Transfus       Date:  2013-11-15       Impact factor: 3.443

5.  Molecular definition of red cell Rh haplotypes by tightly linked SphI RFLPs.

Authors:  C H Huang; M E Reid; Y Chen; G Coghlan; Y Okubo
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

Review 6.  The Rh protein family: gene evolution, membrane biology, and disease association.

Authors:  Cheng-Han Huang; Mao Ye
Journal:  Cell Mol Life Sci       Date:  2009-12-02       Impact factor: 9.261

7.  Molecular genetics of chimpanzee Rh-related genes: their relationship with the R-C-E-F blood group system, the chimpanzee counterpart of the human rhesus system.

Authors:  I Salvignol; A Blancher; P Calvas; J Clayton; W W Socha; Y Colin; J Ruffié
Journal:  Biochem Genet       Date:  1994-06       Impact factor: 1.890

8.  Erythrocyte membrane proteins reactive with human (warm-reacting) anti-red cell autoantibodies.

Authors:  J P Leddy; J L Falany; G E Kissel; S T Passador; S I Rosenfeld
Journal:  J Clin Invest       Date:  1993-04       Impact factor: 14.808

9.  Lack of the Rhesus protein Rh1 impairs growth of the green alga Chlamydomonas reinhardtii at high CO2.

Authors:  Eric Soupene; William Inwood; Sydney Kustu
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-19       Impact factor: 11.205

10.  An Rh1-GFP fusion protein is in the cytoplasmic membrane of a white mutant strain of Chlamydomonas reinhardtii.

Authors:  Corinne Yoshihara; Kentaro Inoue; Denise Schichnes; Steven Ruzin; William Inwood; Sydney Kustu
Journal:  Mol Plant       Date:  2008-11-14       Impact factor: 13.164

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