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Characterization of the human sex hormone binding globulin (SHBG) gene and demonstration of two transcripts in both liver and testis

Gershagen, S.; Lundwall, Åke LU and Fernlund, Per LU (1989) In Nucleic Acids Research 17(22). p.58-9245
Abstract
A genomic cosmid clone for human sex hormone binding globulin (SHBG), a liver-secreted plasma glycoprotein that binds sex steroids, was isolated with a previously characterized liver cDNA as probe. Southern blot analysis of genomic DNA indicated that only one SHBG gene is present in the human haploid genome. A 3.8 Kb Xba I-fragment of the clone containing the entire coding region of SHBG was sequenced. The SHBG gene has 8 exons. The 5'-end preceding the translation start site had no TATA box or CAAT box promoter elements. Screening of a human testis cDNA library resulted in the isolation of two distinct cDNA forms. One cDNA was identical with the previously characterized liver SHBG cDNA, thus suggesting that human SHBG and the androgen... (More)
A genomic cosmid clone for human sex hormone binding globulin (SHBG), a liver-secreted plasma glycoprotein that binds sex steroids, was isolated with a previously characterized liver cDNA as probe. Southern blot analysis of genomic DNA indicated that only one SHBG gene is present in the human haploid genome. A 3.8 Kb Xba I-fragment of the clone containing the entire coding region of SHBG was sequenced. The SHBG gene has 8 exons. The 5'-end preceding the translation start site had no TATA box or CAAT box promoter elements. Screening of a human testis cDNA library resulted in the isolation of two distinct cDNA forms. One cDNA was identical with the previously characterized liver SHBG cDNA, thus suggesting that human SHBG and the androgen binding protein (ABP) produced by Sertoli cells are coded for by the same gene. The second cDNA differed from the first by having exon I exchanged with a completely different sequence and exon VII deleted. An exon coding for the 5'-end of this cDNA was found in the cosmid clone 1.5 kb upstream of the first SHBG exon. Primer extension experiments showed the alternatively spliced transcript corresponding to the second cDNA to be present in both liver and testis. From the primary structure of this putative SHBG-gene-related protein, it may be deduced that it is a protein very different from SHBG and probably without steroid binding activity. (Less)
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organization
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Contribution to journal
publication status
published
subject
keywords
Oligonucleotide Probes, Molecular Sequence Data, Male, Liver/*metabolism, Humans, *Genes, DNA/genetics, Cosmids, Molecular, Cloning, Northern, Blotting, Amino Acid Sequence, Base Sequence, Research Support, Non-U.S. Gov't, Restriction Mapping, Sex Hormone-Binding Globulin/*genetics, Testis/*metabolism, *Transcription, Genetic
in
Nucleic Acids Research
volume
17
issue
22
pages
58 - 9245
publisher
Oxford University Press
external identifiers
  • Scopus:0024369176
ISSN
1362-4962
language
English
LU publication?
yes
id
3d4c533b-0b5e-4282-8a09-ab6005ce74d4 (old id 3965168)
alternative location
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=2587256
date added to LUP
2013-08-11 15:06:36
date last changed
2016-11-17 15:50:27
@misc{3d4c533b-0b5e-4282-8a09-ab6005ce74d4,
  abstract     = {A genomic cosmid clone for human sex hormone binding globulin (SHBG), a liver-secreted plasma glycoprotein that binds sex steroids, was isolated with a previously characterized liver cDNA as probe. Southern blot analysis of genomic DNA indicated that only one SHBG gene is present in the human haploid genome. A 3.8 Kb Xba I-fragment of the clone containing the entire coding region of SHBG was sequenced. The SHBG gene has 8 exons. The 5'-end preceding the translation start site had no TATA box or CAAT box promoter elements. Screening of a human testis cDNA library resulted in the isolation of two distinct cDNA forms. One cDNA was identical with the previously characterized liver SHBG cDNA, thus suggesting that human SHBG and the androgen binding protein (ABP) produced by Sertoli cells are coded for by the same gene. The second cDNA differed from the first by having exon I exchanged with a completely different sequence and exon VII deleted. An exon coding for the 5'-end of this cDNA was found in the cosmid clone 1.5 kb upstream of the first SHBG exon. Primer extension experiments showed the alternatively spliced transcript corresponding to the second cDNA to be present in both liver and testis. From the primary structure of this putative SHBG-gene-related protein, it may be deduced that it is a protein very different from SHBG and probably without steroid binding activity.},
  author       = {Gershagen, S. and Lundwall, Åke and Fernlund, Per},
  issn         = {1362-4962},
  keyword      = {Oligonucleotide Probes,Molecular Sequence Data,Male,Liver/*metabolism,Humans,*Genes,DNA/genetics,Cosmids,Molecular,Cloning,Northern,Blotting,Amino Acid Sequence,Base Sequence,Research Support,Non-U.S. Gov't,Restriction Mapping,Sex Hormone-Binding Globulin/*genetics,Testis/*metabolism,*Transcription,Genetic},
  language     = {eng},
  number       = {22},
  pages        = {58--9245},
  publisher    = {ARRAY(0xaba7228)},
  series       = {Nucleic Acids Research},
  title        = {Characterization of the human sex hormone binding globulin (SHBG) gene and demonstration of two transcripts in both liver and testis},
  volume       = {17},
  year         = {1989},
}