Literature DB >> 1427854

Identification of three new genes and estimation of the size of the carcinoembryonic antigen family.

W N Khan1, L Frängsmyr, S Teglund, A Israelsson, K Bremer, S Hammarström.   

Abstract

Using carcinoembryonic antigen (CEA) subgroup-specific degenerate PCR primers, we have identified three new CEA gene family member L/N exons (CGM9, CGM10, and CGM11) and all previously reported L/N exons of the CEA subgroup (CEA, BGP, NCA, CGM1, CGM2, CGM6, CGM7, and CGM8). This suggests that the CEA subgroup contains 11 genes. CGM9, CGM10, and CGM11 seem to be pseudogenes. A deletion of an asparagine in CGM9 results in loss of a glycosylation site, which is conserved throughout the CEA gene family. We have previously suggested the number of genes in the pregnancy-specific glycoprotein (PSG) subgroup to be 11, which together with this study indicates that the CEA gene family contains 22 genes in all. Parsimony analysis of the CEA subgroup interrelationships suggests that CGM7 occupies the most primitive position within the CEA subgroup, being a sister group to the rest. CEA, BGP, NCA, and CGM1 form a fairly well-supported group within the CEA subgroup.

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Year:  1992        PMID: 1427854     DOI: 10.1016/s0888-7543(05)80230-7

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  Differential recognition of members of the carcinoembryonic antigen family by Opa variants of Neisseria gonorrhoeae.

Authors:  M P Bos; F Grunert; R J Belland
Journal:  Infect Immun       Date:  1997-06       Impact factor: 3.441

2.  Evidence of changes in the immunophenotype and metabolic characteristics (intracellular reactive oxygen radicals) of fetal, but not maternal, monocytes and granulocytes in the fetal inflammatory response syndrome.

Authors:  Sun Kwon Kim; Roberto Romero; Tinnakorn Chaiworapongsa; Juan Pedro Kusanovic; Shali Mazaki-Tovi; Pooja Mittal; Offer Erez; Edi Vaisbuch; Francesca Gotsch; Percy Pacora; Lami Yeo; Maria Teresa Gervasi; Ronald F Lamont; Bo Hyun Yoon; Sonia S Hassan
Journal:  J Perinat Med       Date:  2009       Impact factor: 1.901

3.  CEACAM6 gene variants in inflammatory bowel disease.

Authors:  Jürgen Glas; Julia Seiderer; Christoph Fries; Cornelia Tillack; Simone Pfennig; Maria Weidinger; Florian Beigel; Torsten Olszak; Ulrich Lass; Burkhard Göke; Thomas Ochsenkühn; Christiane Wolf; Peter Lohse; Bertram Müller-Myhsok; Julia Diegelmann; Darina Czamara; Stephan Brand
Journal:  PLoS One       Date:  2011-04-29       Impact factor: 3.240

4.  Synthetic peptides from the N-domains of CEACAMs activate neutrophils.

Authors:  K M Skubitz; K D Campbell; A P Skubitz
Journal:  J Pept Res       Date:  2001-12

5.  Interdependency of CEACAM-1, -3, -6, and -8 induced human neutrophil adhesion to endothelial cells.

Authors:  Keith M Skubitz; Amy P N Skubitz
Journal:  J Transl Med       Date:  2008-12-10       Impact factor: 5.531

6.  Tumor and endothelial cell-derived microvesicles carry distinct CEACAMs and influence T-cell behavior.

Authors:  Harrison T Muturi; Janine D Dreesen; Elena Nilewski; Holger Jastrow; Bernd Giebel; Suleyman Ergun; Bernhard B Singer
Journal:  PLoS One       Date:  2013-09-11       Impact factor: 3.240

  6 in total

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