Complete sequencing of the Fugu WAGR region from WT1 to PAX6: Dramatic compaction and conservation of synteny with human chromosome 11p13
- Colin Miles*,
- Greg Elgar†,
- Edward Coles†,
- Dirk-Jan Kleinjan*,
- Veronica van Heyningen*, and
- Nicholas Hastie*,‡
- *Medical Research Council Human Genetics Unit, Western General Hospital, Edinburgh EH4 2XU, United Kingdom; and †United Kingdom Human Genome Mapping Project Resource Centre, Hinxton, Cambridge CB10 1SB, United Kingdom
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Communicated by Sydney Brenner, The Molecular Sciences Institute, Inc., Berkeley, CA (received for review February 8, 1998)
Abstract
The pufferfish Fugu rubripes has a genome ≈7.5 times smaller than that of mammals but with a similar number of genes. Although conserved synteny has been demonstrated between pufferfish and mammals across some regions of the genome, there is some controversy as to what extent Fugu will be a useful model for the human genome, e.g., [Gilley, J., Armes, N. & Fried, M. (1997) Nature (London) 385, 305–306]. We report extensive conservation of synteny between a 1.5-Mb region of human chromosome 11 and <100 kb of the Fugu genome in three overlapping cosmids. Our findings support the idea that the majority of DNA in the region of human chromosome 11p13 is intergenic. Comparative analysis of three unrelated genes with quite different roles, WT1, RCN1, and PAX6, has revealed differences in their structural evolution. Whereas the human WT1 gene can generate 16 protein isoforms via a combination of alternative splicing, RNA editing, and alternative start site usage, our data predict that Fugu WT1 is capable of generating only two isoforms. This raises the question of the extent to which the evolution of WT1 isoforms is related to the evolution of the mammalian genitourinary system. In addition, this region of the Fugu genome shows a much greater overall compaction than usual but with significant noncoding homology observed at the PAX6 locus, implying that comparative genomics has identified regulatory elements associated with this gene.
Footnotes
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↵ ‡ To whom reprint requests should be addressed. e-mail: Oldnick{at}hgu.mrc.ac.uk.
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Data deposition: The sequence reported in this paper has been deposited in the GenBank database (accession no. AL021531 for the sequence of cosmid 151-J19).
- ABBREVIATIONS:
- WAGR syndrome,
- Wilms’ tumor, Aniridia, Genitourinary abnormalities and mental Retardation;
- HGMP-RC,
- Human Genome Mapping Project Resource Centre
- Copyright © 1998, The National Academy of Sciences





