Genome Res. 14:1861-1869, 2004
©2004 by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/04 $5.00
Letter
Inverted Repeat Structure of the Human Genome: The X-Chromosome Contains a Preponderance of Large, Highly Homologous Inverted Repeats That Contain Testes Genes
Peter E. Warburton1,4,
Joti Giordano1,
Fanny Cheung1,
Yefgeniy Gelfand3 and
Gary Benson2,3
1 Department of Human Genetics, Mount Sinai School of Medicine, New York, New York 10029, USA
2 Department of Computer Science, Department of Biology, Boston University, Boston, Massachusetts 02215, USA
3 Laboratory for Biocomputing and Informatics, Boston University, Boston, Massachusetts 02215, USA
We have performed the first genome-wide analysis of the Inverted Repeat (IR) structure in the human genome, using a novel and efficient software package called Inverted Repeats Finder (IRF). After masking of known repetitive elements, IRF detected 22,624 human IRs characterized by arm size from 25 bp to >100 kb with at least 75% identity, and spacer length up to 100 kb. This analysis required 6 h on a desktop PC. In all, 166 IRs had arm lengths >8 kb. From this set, IRs were excluded if they were in unfinished/unassembled regions of the genome, or clustered with other closely related IRs, yielding a set of 96 large IRs. Of these, 24 (25%) occurred on the X-chromosome, although it represents only 5% of the genome. Of the X-chromosome IRs, 83.3% were 99% identical, compared with 28.8% of autosomal IRs. Eleven IRs from Chromosome X, one from Chromosome 11, and seven already described from Chromosome Y contain genes predominantly expressed in testis. PCR analysis of eight of these IRs correctly amplified the corresponding region in the human genome, and six were also confirmed in gorilla or chimpanzee genomes. Similarity dot-plots revealed that 22 IRs contained further secondary homologous structures partially categorized into three distinct patterns. The prevalence of large highly homologous IRs containing testes genes on the X- and Y-chromosomes suggests a possible role in male germ-line gene expression and/or maintaining sequence integrity by gene conversion.
4 Corresponding author. E-MAIL peter.warburton{at}mssm.edu; FAX (212) 849-2508.
[Supplemental material is available online at www.genome.org.]
Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.2542904.

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