The KH domain is a region defined by its homology to the RNA-binding domain
s of the heterogeneous nuclear ribonucleoprotein K (hnRNPK), There are two
such domains in the FMR1 protein which is underexpressed in the fragile X s
yndrome. We developed a computer method to search the S. cerevisiae protein
sequences as they became available for the KH domain of the FMR1 protein.
Using our motif and FINDPATTERNS of the Wisconsin Package of GCG, nine prot
eins were identified in the completed yeast ORF database that contain KH do
mains. Five proteins have known or predicted functions; four await function
al analysis. Using GeneWorks and GeneJockeyII alignments, we found that the
yeast protein KH domain showing the most similarity to either FMR1P KH dom
ain was a KH domain in HX/SCP160. Its sequence is 50% identical to the seco
nd KH domain of FMR1P, However, SCP160 contains eight conserved and six deg
enerate KH domains. Further analysis showed that SCP160 is a better match o
verall to the vertebrate and C. elegans protein Vigilin, which also contain
s 14 KH domains. The next most similar yeast KH domain was found in YB83, a
protein shorter than FMR1P and containing three KH domains, one of which s
hares 45% identity with the second KH domain in FMR1P. There is no signific
ant overall sequence similarity between this yeast protein and FMR1P. Thus,
while several proteins in yeast contain KH domains, no apparent yeast homo
logue exists for the FMR1 protein of the fragile X gene family. (C) 1999 Wi
ley-Liss, Inc.