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Human follicle-stimulating hormone beta-subunit gene encodes multiple messenger ribonucleic acids
J L Jameson1, C B Becker, C M Lindell
1Thyroid Unit, Massachusetts General Hospital, Boston.
Molecular Endocrinology (Baltimore, Md.)
|September 1, 1988
Summary
Researchers characterized the human Follicle-Stimulating Hormone (FSH) beta gene, revealing a single gene locus. This gene generates multiple FSH beta mRNA transcripts through alternative splicing and polyadenylation, all encoding identical peptides.
Area of Science:
- Molecular Biology
- Genetics
- Endocrinology
Background:
- Follicle-Stimulating Hormone (FSH) is a crucial pituitary gonadotropin.
- FSH is synthesized from separate alpha- and beta-subunit genes.
- Understanding the human FSH beta gene structure is key to comprehending FSH regulation.
Purpose of the Study:
- To isolate and characterize the complete human FSH beta gene.
- To elucidate the transcriptional unit and regulatory elements of the FSH beta gene.
- To investigate the mechanisms of mRNA processing for FSH beta.
Main Methods:
- Isolation of a 12 kb DNA fragment containing the human FSH beta gene from a genomic DNA library.
- Nucleotide sequencing of the FSH beta gene.
- Southern blot analysis of human genomic DNA.
- Analysis of transcriptional unit, introns, exons, and polyadenylation sites.
Main Results:
- The human FSH beta gene spans 3.9 kb and contains two introns.
- Alternative splicing of the first exon generates two 5'-untranslated regions (Exon IA and IB).
- Two distinct polyadenylation sites are utilized, with one leading to a long 3'-untranslated sequence.
- At least four distinct FSH beta mRNA species are processed from a single gene, all encoding identical peptides.
- Similar mRNA distributions were observed in normal pituitary tissue and pituitary adenomas.
Conclusions:
- The human FSH beta gene exhibits complex mRNA processing through alternative splicing and polyadenylation.
- Despite transcript diversity, all processed mRNAs encode identical FSH beta peptides.
- These findings provide insights into the molecular basis of FSH production and regulation.