» Articles » PMID: 7736276

Detection of Primary and Mature Transcripts of Calcitonin-gene-related Peptide Genes in Rat Parafollicular Cells by Light, Fluorescence and Confocal Microscopy

Overview
Publisher Springer
Date 1995 Jan 1
PMID 7736276
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Alternative splicing of primary transcripts from the calcitonin/alpha calcitonin gene-related peptide (alpha CGRP) gene result in mature mRNAs encoding either calcitonin or alpha CGRP. We have produced sequence-specific, synthetic, biotinylated oligodeoxynucleotide probes that recognize calcitonin (exon 4), and alpha CGRP (exon 6) sequences as well as sequences common to both splice variants (exon 3) of this gene. Probes to exons 4 and 3 revealed strong cytoplasmic signals in rat parafollicular cells. In addition, a punctate nuclear signal was obtained with these probes. The alpha CGRP-specific (exon 6) probe resulted in weak cytoplasmic labelling of parafollicular cells, but produced a punctate nuclear labelling similar to that seen with the exon 4 and 3 probes. RNase digestion removed all the cytoplasmic and nuclear signals obtained with all probes. Hybridization with a thyroglobulin-specific probe failed to label parafollicular cells. A control (human enterovirus) probe yielded negative results, while a probe to rat somatostatin produced cytoplasmic labelling of a small subpopulation of parafollicular cells. Finally, a probe specific for beta CGRP mRNA labelled most, if not all, parafollicular cells. Fluorescent alkaline phosphatase development of in situ hybridizations could be combined with indirect immunofluorescence for CGRP. Analysis by fluorescence and confocal microscopy revealed that CGRP immunoreactive cells contained calcitonin, alpha CGRP and beta CGRP hybridization signals. Our results demonstrate that all three genes may be simultaneously expressed by thyroid parafollicular cells and show that synthetic biotinylated oligonucleotide probes can be used for highly precise localizations of primary transcripts in the nuclei of these cells.(ABSTRACT TRUNCATED AT 250 WORDS)

Citing Articles

Downregulating lncRNA NEAT1 induces proliferation and represses apoptosis of ovarian granulosa cells in polycystic ovary syndrome via microRNA-381/IGF1 axis.

Zhen J, Li J, Li X, Wang X, Xiao Y, Sun Z J Biomed Sci. 2021; 28(1):53.

PMID: 34266430 PMC: 8281489. DOI: 10.1186/s12929-021-00749-z.


FGF5 Regulates Schwann Cell Migration and Adhesion.

Chen B, Hu R, Min Q, Li Y, Parkinson D, Dun X Front Cell Neurosci. 2020; 14:237.

PMID: 32848626 PMC: 7417478. DOI: 10.3389/fncel.2020.00237.

References
1.
Denijn M, de Weger R, Lips C, Van Unnik J, Den Otter W . Hybridohistochemical demonstration of alternative splicing of the CALC-I gene. Am J Pathol. 1991; 138(2):273-7. PMC: 1886184. View

2.
Raap A, van de Rijke F, Dirks R, Sol C, BOOM R, VAN DER PLOEG M . Bicolor fluorescence in situ hybridization to intron and exon mRNA sequences. Exp Cell Res. 1991; 197(2):319-22. DOI: 10.1016/0014-4827(91)90439-2. View

3.
Di Lauro R, Obici S, Condliffe D, Ursini V, Musti A, Moscatelli C . The sequence of 967 amino acids at the carboxyl-end of rat thyroglobulin. Location and surroundings of two thyroxine-forming sites. Eur J Biochem. 1985; 148(1):7-11. DOI: 10.1111/j.1432-1033.1985.tb08799.x. View

4.
JONAS V, Lin C, Kawashima E, Semon D, Swanson L, Mermod J . Alternative RNA processing events in human calcitonin/calcitonin gene-related peptide gene expression. Proc Natl Acad Sci U S A. 1985; 82(7):1994-8. PMC: 397471. DOI: 10.1073/pnas.82.7.1994. View

5.
Xing Y, Johnson C, Dobner P, Lawrence J . Higher level organization of individual gene transcription and RNA splicing. Science. 1993; 259(5099):1326-30. DOI: 10.1126/science.8446901. View