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Molecular and Cellular Endocrinology
Volume 84, Issues 1-2, March 1992, Pages R23-R26
 
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doi:10.1016/0303-7207(92)90087-M    How to Cite or Link Using DOI (Opens New Window)
Copyright © 1992 Published by Elsevier Science Ireland Ltd.

Rapid paper

Identification of a minor Tg mRNA transcript in RNA from normal and goitrous thyroids

Héctor M. Targovnika, Corresponding Author Contact Information, Pascale Cochauxb, Daniel Corachc and Gilbert Vassartc, b

a Catedra de Genética y Biologia Molecular, Facultad de Farmacia y Bioquimica, Uniuersidad de Buenos Aires, 1113, Buenos Aires, Argentina b Service de Génétique, Hôpital Erasme, Université Libre de Bruxelles, 1070, Brussels, Belgium c I.R.I.B.H.N., Université Libre de Bruxelles, 1070, Brussels, Belgium

Received 24 December 1991; 
accepted 27 December 1991. ;
Available online 6 January 2003.

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Abstract

Polymerase chain reaction (PCR) amplification of nt 4502 to nt 5184 of the thyroglobulin (Tg) mRNA from several patients, with or without elevated serum thyrotropin (TSH), showed a predominant fragment of the expected size (683 bp) and a minor fragment of 512 bp. The sequence of this minor fragment revealed that 171 bp were missing between position 4567 and 4737. It is highly probable that the deleted sequence corresponds to a complete exon, suggesting an alternative splicing as mechanism for the generation of the minor transcript.

Author Keywords: Thyroglobulin gene; Thyroglobulin mRNA; Deletion; Molecular variant; Thyroid, human; Polymerase chain reaction

Abbreviations: Tg, thyroglobulin; TPO, thyroperoxidase; TSH, thyrotropin; PCR, polymerase chain reaction; RT, reverse transcription; nt, nucleotide; kb, 103 bases; bp, base pairs; dNTP, deoxyribonucleotide triphosphate; nt numbering starts at nt 1 of Tg mRNA, amino acid numbering corresponds to that of the mature protein without the leader peptide

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