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Differential usage of three exons generates at least five different mRNAs encoding human leukocyte common antigens
Leukocyte common antigens (LCAs, also known as T200 and CD 45) are integral membrane proteins expressed exclusively on hematopoietic cells. These molecules exhibit varying molecular masses and epitopes when expressed in different cell types. To determine the genetic bases for the generation of this...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1987
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189669/ https://www.ncbi.nlm.nih.gov/pubmed/2824653 |
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collection | PubMed |
description | Leukocyte common antigens (LCAs, also known as T200 and CD 45) are integral membrane proteins expressed exclusively on hematopoietic cells. These molecules exhibit varying molecular masses and epitopes when expressed in different cell types. To determine the genetic bases for the generation of this diversity, three classes of human LCA cDNA clones that are different near their 5' ends have been isolated. These differences arose as a result of differential usage of three exons as determined from an analysis of a genomic DNA clone. Furthermore, Northern blot analysis with LCA exon-specific probes demonstrates the existence of at least two more LCA mRNA forms that are generated by differential splicing. A comparison of the human and mouse LCA protein sequences revealed a marked difference only in the extracellular domain. |
format | Text |
id | pubmed-2189669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1987 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21896692008-04-17 Differential usage of three exons generates at least five different mRNAs encoding human leukocyte common antigens J Exp Med Articles Leukocyte common antigens (LCAs, also known as T200 and CD 45) are integral membrane proteins expressed exclusively on hematopoietic cells. These molecules exhibit varying molecular masses and epitopes when expressed in different cell types. To determine the genetic bases for the generation of this diversity, three classes of human LCA cDNA clones that are different near their 5' ends have been isolated. These differences arose as a result of differential usage of three exons as determined from an analysis of a genomic DNA clone. Furthermore, Northern blot analysis with LCA exon-specific probes demonstrates the existence of at least two more LCA mRNA forms that are generated by differential splicing. A comparison of the human and mouse LCA protein sequences revealed a marked difference only in the extracellular domain. The Rockefeller University Press 1987-11-01 /pmc/articles/PMC2189669/ /pubmed/2824653 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Differential usage of three exons generates at least five different mRNAs encoding human leukocyte common antigens |
title | Differential usage of three exons generates at least five different mRNAs encoding human leukocyte common antigens |
title_full | Differential usage of three exons generates at least five different mRNAs encoding human leukocyte common antigens |
title_fullStr | Differential usage of three exons generates at least five different mRNAs encoding human leukocyte common antigens |
title_full_unstemmed | Differential usage of three exons generates at least five different mRNAs encoding human leukocyte common antigens |
title_short | Differential usage of three exons generates at least five different mRNAs encoding human leukocyte common antigens |
title_sort | differential usage of three exons generates at least five different mrnas encoding human leukocyte common antigens |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189669/ https://www.ncbi.nlm.nih.gov/pubmed/2824653 |