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Methods to Discover Alternative Promoter Usage and Transcriptional Regulation of Murine Bcrp1
Published on: May 27, 2016
Expression of the two alternatively spliced PRKAR1A RNAs in human endocrine glands
Erika Peverelli1, Giovanna Mantovani, Sara Bondioni
1Institute of Endocrine Sciences, University of Milan, Ospedale Maggiore IRCCS, Padiglione Granelli, Via F. Sforza, 35, 20122 Milan, Italy.
Abstract:
Heterozygous loss of function mutations in human PKAR1A gene (PRKAR1A) have been identified in patients with Carney complex (CNC), an autosomal dominant familial multiple neoplasia syndrome displaying different endocrine tumors, including adrenocortical tumors, GH-secreting pituitary tumors and thyroid adenomas. Although PRKAR1A is encoded by a single gene, it is transcribed from at least two different promoters, adjacent to different first non-coding exons (1a and 1b), giving rise to alternately spliced transcripts coding for identical proteins. The separate regulation of the two distinct promoters and the presence of multiple alternatively spliced first exons suggest a complex mechanism of PRKAR1A expression regulation. In order to investigate the relative expression of the two mRNA transcripts (1a and 1b) in human adult endocrine tissues involved in the determination of CNC phenotype, we selected 17 pituitary, 20 adrenal and seven thyroid tissues from tumoral and peri-tumoral lesion samples. Expression of the two transcripts was evaluated by semi-quantitative RT-PCR and real-time RT-PCR. This study first reports that human pituitary and thyroid tissues show a similar expression of the two transcripts, whereas in adrenal tissues transcript 1b is the most abundant one.
Insights
Mutations in the PRKAR1A gene cause Carney complex (CNC). This study reveals differential expression of PRKAR1A transcripts in endocrine tissues, with transcript 1b dominant in adrenal glands.
Area of Science:
- Endocrinology
- Molecular Biology
- Genetics
Background:
- Carney complex (CNC) is an autosomal dominant syndrome linked to PRKAR1A gene mutations.
- PRKAR1A exhibits complex expression via two promoters and alternative splicing.
- Understanding PRKAR1A transcript regulation is crucial for CNC pathogenesis.
Purpose of the Study:
- To investigate the relative expression of PRKAR1A mRNA transcripts (1a and 1b) in human adult endocrine tissues.
- To correlate PRKAR1A expression patterns with tissues implicated in Carney complex.
Main Methods:
- Semi-quantitative and real-time RT-PCR were used to analyze PRKAR1A transcript levels.
- Samples included pituitary, adrenal, and thyroid tissues from tumoral and peri-tumoral lesions.
Main Results:
- Pituitary and thyroid tissues demonstrated similar expression levels for both PRKAR1A transcripts (1a and 1b).
- Adrenal tissues showed a significantly higher abundance of transcript 1b compared to transcript 1a.
Conclusions:
- PRKAR1A expression is tissue-specific, with transcript 1b predominating in the adrenal gland.
- These findings highlight complex gene regulation and tissue-specific roles of PRKAR1A in endocrine neoplasia.
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