Journal Article

Did nucleotides or amino acids drive evolutionary conservation of the WT1 ±KTS alternative splice?

Rachel C. Davies, Eva Bratt and Nicholas D. Hastie

in Human Molecular Genetics

Volume 9, issue 8, pages 1177-1183
Published in print May 2000 | ISSN: 0964-6906
Published online May 2000 | e-ISSN: 1460-2083 | DOI:
Did nucleotides or amino acids drive evolutionary conservation of the WT1 ±KTS alternative splice?

Show Summary Details


Evolutionary comparisons frequently pinpoint crucial parts of a protein but, even within coding regions, nucleotides can do more than determine amino acid sequence. One highly conserved feature of the Wilms’ tumour suppressor gene, WT1, is the potential, following alternative pre-mRNA splicing, to insert three amino acids (KTS) between the third and fourth zinc fingers. The nucleotides at this position simultaneously define amino acids and the alternative splice site. At the protein level this insertion influences DNA binding affinity and specificity, protein–protein interactions and subnuclear localization. Mutations within the ±KTS splice junction lead to severe urogenital developmental abnormalities such as Frasier syndrome, indicating that the isoform ratio is critical for wild-type function. Using a series of site-directed mutations in both the genomic and cDNA context, the nucleotide–amino acid relationship was investigated. Mutational analysis within the cDNA suggests that the precise amino acids inserted may not be critical, but rather the disruption of the zinc finger structure alone may be sufficient to generate proteins with different in vitro properties. However, analysis within the genomic context suggests that the precise structure of the splice junction is crucial in retaining the balance between the isoforms, and this may account for the high nucleo­tide conservation of this unusual gene structure from fish to mammals.

Journal Article.  5734 words.  Illustrated.

Subjects: Genetics and Genomics

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.