We mapped 75 genes that collectively encode >90% of the proteins Found
in human ribosomes. Because localization of ribosomal protein genes (
rp genes) is complicated by the existence of processed pseudogenes, mu
ltiple strategies were devised to identify PCR-detectable sequence-tag
ged sites (STSs) at introns. In some cases we exploited specific, pre-
existing information about the intron/exon structure of a given human
rp gene or its homolog in another vertebrate. When such information wa
s unavailable, selection of PCR primer pairs was guided by general ins
ights gleaned h-om analysis of all mammalian rp genes whose intron/exo
n structures have been published, for many genes, PCR amplification of
introns was facilitated by use of YAC pool DNAs rather than total hum
an genomic DNA as templates. We then assigned the rp gene STSs to indi
vidual human chromosomes by typing human-rodent hybrid cell lines. The
genes were placed more precisely on the physical map of the human gen
ome by typing of radiation hybrids or screening YAC libraries. fifty-o
ne previously unmapped rp genes were localized, and 24 previously repo
rted rp gene localizations were confirmed, refined, or corrected. Thou
gh functionally related and coordinately expressed, the 75 mapped gene
s are widely dispersed: Both sex chromosomes and at least 20 of the 22
autosomes carry one or more rp genes. Chromosome 19, known to have a
high gene density, contains an unusually large number of rp genes (12)
. This map provides a Foundation For the study of the possible roles o
f ribosomal protein deficiencies in chromosomal and Mendelian disorder
s.