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Journal of Endocrinology (1988) 117, 161-165    DOI: 10.1677/joe.0.1170161
© 1988 Society for Endocrinology

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Thyrotrophin gene regulation

J. A. Franklyn and M. C. Sheppard

Department of Medicine, University of Birmingham, Queen Elizabeth Hospital, Edgbaston, Birmingham B15 2TH

RECEIVED 1 November 1987

Introduction: Thyrotrophin (TSH) is one of a family of glycoprotein hormones which includes the pituitary hormones follicle-stimulating hormone and luteinizing hormone, and placental chorionic gonadotrophin. Each hormone is composed of two dissimilar, non-covalently linked glycosylated subunits, {alpha} and β. The mammalian genome contains a single gene encoding the {alpha}-subunit which is common to each of the glycoprotein hormones (Fiddes & Goodman, 1981). In contrast, the β-subunits of each hormone are encoded by different genes and confer biological and immunological specificity upon the intact dimer.

The gene encoding the β-subunit of TSH has been assigned to chromosome 1 in man (Fukushige, Murotsu & Matsubara, 1986) and chromosome 3 in the mouse (Kourides, Barker, Gurr et al. 1984). The {alpha}-gene, unlike the β-gene, has been assigned in the mouse to chromosome 4 (Kourides et al.







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