Huge Splicing Frequency in Human Y Chromosomal UTY Gene
To cite this article: Ingeborg Laaser, Fabian J. Theis, Martin Hrabé de Angelis, Hans-Jochem Kolb, and Jerzy Adamski. OMICS: A Journal of Integrative Biology.
March 2011,
15(3): 141-154.
doi:10.1089/omi.2010.0107.
Published in Volume: 15 Issue 3: March 6, 2011 Online Ahead of Print: February 17, 2011
Ingeborg Laaser,1 Fabian J. Theis,2 Martin Hrabé de Angelis,1,4 Hans-Jochem Kolb,3 and Jerzy Adamski1,4
1Helmholtz Zentrum München, German Research Center for Environmental Health, Institute of Experimental Genetics, Genome Analysis Center, Neuherberg, Germany.
2Institute of Bioinformatics and Systems Biology, Neuherberg, Germany.
3Clinical Cooperative Group, Haematopoietic Cell Transplantation, José-Carreras Transplantation Unit, Ludwig Maximilians-Universität, Munich, Germany.
4Lehrstuhl für Experimentelle Genetik, Technische Universität München, Freising-Weihenstephan, Germany.
Over 90% of human genes produce more than one mRNA by alternative splicing (AS). Human UTY (ubiquitously transcribed tetratricopeptide repeat protein on the chromosome Y) has six mRNA-transcripts. UTY is subject to interdisciplinary approaches such as Y chromosomal genetics or development of leukemia immunotherapy based on UTY-specific peptides. Investigating UTY expression in a normal and leukemic setting we discovered an exceptional splicing phenomenon fostering huge transcript diversity. Transcript sequencing identified 90 novel AS-events being almost randomly combined in 284 new transcripts. We uncovered a novel system of transcript architecture and genomic organization in UTY. On a basis of a new UTY-splicing multigraph including a mathematical model we calculated the theoretical yield to exceed 1.3 billion distinct transcripts. To our knowledge, this is the greatest estimated transcript diversity by AS. On protein level we demonstrated interaction of AS-derived proteins with new interactors by yeast-two-hybrid assay. For translational research we predicted new UTY-peptide candidates for leukemia therapy development. Our study provides new insights into the complexity of human alternative splicing and its potential contribution to the transcript diversity of the transcriptome.
Patrizia Ferroni, David Della-Morte, Raffaele Palmirotta, Mark McClendon, Gianluca Testa, Pasquale Abete, Franco Rengo, Tatjana Rundek, Fiorella Guadagni, Mario Roselli
Vural Ozdemir, Charles Smith, Kathleen Bongiovanni, David Cullen, Bartha M. Knoppers, Andrew Lowe, Mette Peters, Robert Robbins, Elizabeth Stewart, Gene Yee, Yi-Kuo Yu, Eugene Kolker
OMICS: A Journal of Integrative Biology.
April 2011: 221-225.