Human and mouse DOCK10 splicing isoforms with alternative first coding exon usage are differentially expressed in T and B lymphocytes

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• 作者：Marí ; a José ; Alcaraz-Garcí ; a^a ; Natalia Ruiz-Lafuente^a ; Silvia Sebastiá ; n-Ruiz^a ; Marí ; a Juliana Majado^b ; Consuelo Gonzá ; lez-Garcí ; a^b ; Marí ; a Victoria Bernardo^a ; Marí ; a Rocí ; o Á ; lvarez-Ló ; pez^a ; ^c ; Antonio Parrado^a ; ^{antonio.parrado@carm.es"" rel=""nofollow}
• 关键词：DOCK10 ; Dedicator of cytokinesis ; Guanosine nucleotide exchange factor ; Alternative splicing ; Interleukin-4 ; Article history
• 刊名：Human Immunology
• 出版年：2011
• 出版时间：July 2011
• 年：2011
• 卷：72
• 期：7
• 页码：531-537
• 全文大小：1904 K

文摘

DOCK10 is a member of the dedicator of cytokinesis (DOCK) family of Rho GTPase activators preferentially expressed in lymphocytes. In this paper, we analyzed DOCK10 mRNA diversity produced because of alternative splicing. Alternative first coding exon usage led to 2 main protein-coding transcripts, DOCK10.1 and DOCK10.2. Full-length cDNA clones of both isoforms were obtained from both normal human peripheral blood mononuclear cells and mouse spleen for the first time for human DOCK10.1, mouse DOCK10.1, and mouse DOCK10.2. Human and mouse DOCK10.1 clones corresponded to the protein coding assemblies provided by the National Center for Biotechnology Information as Reference Sequences for DOCK10. Our analysis especially focused on human cDNA clones, of which 63 % were alternatively spliced forms involving diverse exons and introns. DOCK10.1 expression was enriched in normal T cells, and DOCK10.2 expression was enriched in normal B cells and chronic lymphocytic leukemia (CLL) B cells. Both isoforms were upregulated in response to interleukin-4 in B cells, both normal and CLL, but not in T cells. Our data suggest that cell-specific mechanisms regulate expression of the alternative first exon variants of DOCK10 in vertebrates.