A New Gene Family Including DSCR1 (Down Syndrome Candidate Region 1) and ZAKI-4: Characterization from Yeast to Human and Identification of DSCR1-like 2, a Novel Human Member (DSCR1L2)

A new gene family has been identified on the basis of in-depth bioinformatics analysis of the Down syndrome candidate region 1 (DSCR1) gene, located on 21q22.1. We have determined the complete coding sequences of similar genes in Saccharomyces cerevisiae and Caenorhabditis elegans, as well as that o...

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Published inGenomics (San Diego, Calif.) Vol. 64; no. 3; pp. 252 - 263
Main Authors Strippoli, Pierluigi, Lenzi, Luca, Petrini, Massimiliano, Carinci, Paolo, Zannotti, Maria
Format Journal Article
LanguageEnglish
Published San Diego, CA Elsevier Inc 15.03.2000
Elsevier
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Abstract A new gene family has been identified on the basis of in-depth bioinformatics analysis of the Down syndrome candidate region 1 (DSCR1) gene, located on 21q22.1. We have determined the complete coding sequences of similar genes in Saccharomyces cerevisiae and Caenorhabditis elegans, as well as that of a novel human gene, named DSCR1L2 (DSCR1-like 2). Peripheral blood leukocyte cDNA sequencing predicts as its product a 241-amino-acid protein highly similar to products of the human genes DSCR1 and ZAKI-4 (HGMW-approved symbol DSCR1L1). The highest level of expression of DSCR1L2 mRNA was found by Northern blot analysis in heart and skeletal muscles, liver, kidney, and peripheral blood leukocytes (three transcripts of 3.2, 5.2, and 7.5 kb). The gene consists of four exons and spans about 22 kb on chromosome 1 (1p33–p35.3) (Human Chromosome 1, Sanger Centre). Exon/intron organization is highly conserved between DSCR1 and DSCR1L2. Two alternative DSCR1L2 mRNA splicing forms have been recognized, with one lacking 10 amino acids in the middle of the protein. Analysis of expressed sequence tags (ESTs) shows DSCR1L2 expression in fetal tissues (heart, liver, and spleen) and in adenocarcinomas. ESTs related to the murine DSCR1L2 orthologue are found in the 2-cell stage mouse embryo, in developing brain stem and spinal cord, and in thymus and T cells. The most prominent feature identified in the protein family is a central short, unique serine–proline motif (including an ISPPXSPP box), which is strongly conserved from yeast to human but is absent in bacteria. Moreover, homology with the RNA-binding domain was weakly but consistently detected in a stretch of 80 amino acids at the amino-terminus by fine sequence analysis based on tools utilizing both hidden Markov models and BLAST. The identification of this new gene family should allow a better understanding of the functions of the genes belonging to it.
AbstractList A new gene family has been identified on the basis of in-depth bioinformatics analysis of the Down syndrome candidate region 1 (DSCR1) gene, located on 21q22.1. We have determined the complete coding sequences of similar genes in Saccharomyces cerevisiae and Caenorhabditis elegans, as well as that of a novel human gene, named DSCR1L2 (DSCR1-like 2). Peripheral blood leukocyte cDNA sequencing predicts as its product a 241-amino-acid protein highly similar to products of the human genes DSCR1 and ZAKI-4 (HGMW-approved symbol DSCR1L1). The highest level of expression of DSCR1L2 mRNA was found by Northern blot analysis in heart and skeletal muscles, liver, kidney, and peripheral blood leukocytes (three transcripts of 3.2, 5.2, and 7.5 kb). The gene consists of four exons and spans about 22 kb on chromosome 1 (1p33–p35.3) (Human Chromosome 1, Sanger Centre). Exon/intron organization is highly conserved between DSCR1 and DSCR1L2. Two alternative DSCR1L2 mRNA splicing forms have been recognized, with one lacking 10 amino acids in the middle of the protein. Analysis of expressed sequence tags (ESTs) shows DSCR1L2 expression in fetal tissues (heart, liver, and spleen) and in adenocarcinomas. ESTs related to the murine DSCR1L2 orthologue are found in the 2-cell stage mouse embryo, in developing brain stem and spinal cord, and in thymus and T cells. The most prominent feature identified in the protein family is a central short, unique serine–proline motif (including an ISPPXSPP box), which is strongly conserved from yeast to human but is absent in bacteria. Moreover, homology with the RNA-binding domain was weakly but consistently detected in a stretch of 80 amino acids at the amino-terminus by fine sequence analysis based on tools utilizing both hidden Markov models and BLAST. The identification of this new gene family should allow a better understanding of the functions of the genes belonging to it.
Author Strippoli, Pierluigi
Carinci, Paolo
Petrini, Massimiliano
Zannotti, Maria
Lenzi, Luca
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Issue 3
Keywords Chromosomal aberration
Trisomy
Aneuploidy
Homology
Fungi
Conserved sequence
Gene
Multigene family
Ascomycetes
Nematoda
Thallophyta
Human
Splicing
Nucleotide sequence
Chromosome A1
Chromosome G21
Critical region
Tissue specificity
Down syndrome
Protein
Caenorhabditis elegans
Helmintha
Nemathelminthia
Invertebrata
Saccharomyces cerevisiae
Language English
License CC BY 4.0
Copyright 2000 Academic Press.
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Snippet A new gene family has been identified on the basis of in-depth bioinformatics analysis of the Down syndrome candidate region 1 (DSCR1) gene, located on...
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SubjectTerms Adaptor Proteins, Signal Transducing
Amino Acid Motifs
Amino Acid Sequence
Animals
Biological and medical sciences
Blotting, Northern
Caenorhabditis elegans Proteins
Down Syndrome - genetics
DSCR1 gene
DSCR1L2 gene
EST
Exons
Expressed Sequence Tags
Fundamental and applied biological sciences. Psychology
Genes. Genome
Humans
Intracellular Signaling Peptides and Proteins
Mice
Molecular and cellular biology
Molecular genetics
Molecular Sequence Data
Muscle Proteins - genetics
Proteins - genetics
Reverse Transcriptase Polymerase Chain Reaction
Saccharomyces cerevisiae Proteins
Sequence Homology, Amino Acid
ZAKI-4 gene
Title A New Gene Family Including DSCR1 (Down Syndrome Candidate Region 1) and ZAKI-4: Characterization from Yeast to Human and Identification of DSCR1-like 2, a Novel Human Member (DSCR1L2)
URI https://dx.doi.org/10.1006/geno.2000.6127
https://www.ncbi.nlm.nih.gov/pubmed/10756093
https://search.proquest.com/docview/17522163
https://search.proquest.com/docview/71070852
Volume 64
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