Identification and regional localization of a human IMP dehydrogenase-like locus (IMPHDL1) at 16p13. 13

Sequence-tagged sites (STS)s are versatile chromosomal markers for a variety of genome mapping efforts. In this report, the authors describe a randomly generated STS (323F4) from human chromosome 16 genomic DNA that has 90.0% sequence identity to the type I human inosine-5[prime]-monophosphate dehyd...

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Published inGenomics (San Diego, Calif.) Vol. 18:3
Main Authors Doggett, N.A., Tesmer, J.G., Duesing, L.A., Callen, D.F., Chen, Z.L., Moore, S., Stallings, R.L.
Format Journal Article
LanguageEnglish
Published United States 01.12.1993
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Abstract Sequence-tagged sites (STS)s are versatile chromosomal markers for a variety of genome mapping efforts. In this report, the authors describe a randomly generated STS (323F4) from human chromosome 16 genomic DNA that has 90.0% sequence identity to the type I human inosine-5[prime]-monophosphate dehydrogenase (IMPDH1) gene and 72% identity to the type II human inosine-5[prime]-monophosphate dehydrogenase (IMPDH2) gene. Additional sequencing by primer walking has provided a total of 1380 bp of the human chromosome 16 sequence. The IMPDH-like sequence 323F4 was regionally localized by PCR analysis of a panel of somatic cell hybrids containing different portions of human chromosome 16 to 16p13.3-13.12, between the breakpoints found in hybrids CY196/CY197 and CY198. This regional mapping assignment was further refined to subband 16p13.3 by high-resolution fluorescence in situ hybridization using cosmid 323F4 as a probe. The authors conclude that a third, previously undescribed IMPDH locus, termed IMPDHL1, exists at human chromosome 16p13.13. 11 refs., 2 figs.
AbstractList Sequence-tagged sites (STS)s are versatile chromosomal markers for a variety of genome mapping efforts. In this report, the authors describe a randomly generated STS (323F4) from human chromosome 16 genomic DNA that has 90.0% sequence identity to the type I human inosine-5[prime]-monophosphate dehydrogenase (IMPDH1) gene and 72% identity to the type II human inosine-5[prime]-monophosphate dehydrogenase (IMPDH2) gene. Additional sequencing by primer walking has provided a total of 1380 bp of the human chromosome 16 sequence. The IMPDH-like sequence 323F4 was regionally localized by PCR analysis of a panel of somatic cell hybrids containing different portions of human chromosome 16 to 16p13.3-13.12, between the breakpoints found in hybrids CY196/CY197 and CY198. This regional mapping assignment was further refined to subband 16p13.3 by high-resolution fluorescence in situ hybridization using cosmid 323F4 as a probe. The authors conclude that a third, previously undescribed IMPDH locus, termed IMPDHL1, exists at human chromosome 16p13.13. 11 refs., 2 figs.
Author Duesing, L.A.
Callen, D.F.
Chen, Z.L.
Stallings, R.L.
Doggett, N.A.
Moore, S.
Tesmer, J.G.
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  fullname: Stallings, R.L.
  organization: Univ. of Pittsburgh, PA (United States)
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Snippet Sequence-tagged sites (STS)s are versatile chromosomal markers for a variety of genome mapping efforts. In this report, the authors describe a randomly...
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SubjectTerms 550400 - Genetics
BASIC BIOLOGICAL SCIENCES
CHROMOSOMES
ENZYMES
GENES
GENETIC MAPPING
HUMAN CHROMOSOME 16
HUMAN CHROMOSOMES
MAPPING
NUCLEOTIDE DEHYDROGENASES
ORGANIC COMPOUNDS
OXIDOREDUCTASES
PROTEINS
Title Identification and regional localization of a human IMP dehydrogenase-like locus (IMPHDL1) at 16p13. 13
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