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J Biol Chem, Vol. 273, Issue 32, 20603-20614, August 7, 1998
From the We have cloned and characterized the genomic
structure of the human gene for Myc-associated zinc finger protein
(MAZ), which is located on chromosome 16p11.2. This gene is transcribed
as an mRNA of 2.7 kilobases (kb) that encodes a 60-kDa MAZ protein. A 40-kb cosmid clone was isolated that includes the promoter, five
exons, four introns, and one 3'-untranslated region. All exon-intron
junction sequences conform to the GT/AG rule. The promoter region has
features typical of a housekeeping gene: a high G + C content (88.4%);
a high frequency of CpG dinucleotides, in particular within the region
0.5 kb upstream of the site of initiation of translation; and the
absence of canonical TATA and CAAT boxes. An S1 nuclease protection
assay demonstrated the presence of multiple sites for initiation of
transcription around a site 174 nucleotides (nt) upstream of the ATG
codon and such expression was reflected by the promoter activity of a
MAZ promoter/CAT (chloramphenicol acetyltransferase) reporter gene.
Cis-acting positive and negative elements controlling basal
transcription of the human MAZ gene were found from
nucleotides (nt)
Genomic Organization and Expression of a Human Gene for
Myc-associated Zinc Finger Protein (MAZ)
§,
¶,
,
,
,
Tsukuba Life Science Center, RIKEN, 3-1-1 Koyadai, Tsukuba, Ibaraki 305, Japan, the § Department of
Medical Genetics, China Medical University, Shenyang 110001, China, the
¶ Institute of Applied Biochemistry, University of Tsukuba,
Tsukuba, Ibaraki 305, Japan, the
Department of Molecular
Genetics, Beckman Research Institute of The City of Hope, Duarte,
California 91010, and the ** Department of Neurology, Institute of Brain
Research, Faculty of Medicine, University of Tokyo, Tokyo, Japan
383 to
248 and nt
2500 to
948. Moreover,
positive and negative autoregulatory elements were also identified in
the regions from nt
248 to
189 and from nt
383 to
248 after
co-transfection of HeLa cells with plasmids that carried the
MAZ promoter/CAT construct and the MAZ-expression vector.
Our results indicate that the 5'-end flanking sequences are responsible
for the promoter activities of the MAZ gene.
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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