| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Departments of Psychiatry and Behavioral Science (A.E.B., L.C.S., N.A., E.E.R.) and Endocrinology, Metabolism, and Molecular Medicine (A.E.B., P.K., L.J.), Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611; Department of Neurobiology and Physiology (L.C.S., N.A., J.S.T.), Howard Hughes Medical Institute (N.A., J.S.T.), Northwestern University, Evanston, Illinois 60208; and The Jackson Laboratory (G.C.), Bar Harbor, Maine 04609
Address all correspondence and requests for reprints to: Dr. Eva Redei, Department of Psychiatry and Behavioral Science, Northwestern University Feinberg School of Medicine, 303 East Chicago Avenue, Chicago, Illinois 60611. E-mail: e-redei{at}northwestern.edu.
Thyroid hormones are essential for the regulation of developmental and physiological processes. The genetic factors underlying naturally occurring variability in mammalian thyroid function are, however, only partially understood. Genetic control of thyroid function can be studied with animal models such as the inbred Wistar-Kyoto (WKY) rat strain. Previous studies established that WKY rats have elevated TSH, slightly elevated total T3, and normal total T4 levels compared with Wistar controls. The present study confirmed a persistent 24-h elevation of TSH in WKY rats compared with the Fisher 344 (F344) rat, another inbred strain. Acute T3 challenge (25 µg/100 g body weight ip) suppressed serum TSH and T4 levels in both strains. Quantitative trait locus analysis of elevated TSH in a reciprocally bred WKY x F344 F2 population identified one highly significant locus on chromosome 6 (LOD = 11.7, TSH-1) and one suggestive locus on chromosome 5 (LOD = 2.3, TSH-2). The confidence interval of TSH-1 contains the TSH receptor and type 2 deiodinase genes, and TSH-2 contains the type 1 deiodinase gene. The WKY alleles of each gene contain sequence alterations, but additional studies are indicated to identify the specific gene or genes responsible for altered regulation of the thyroid axis. These findings suggest that one or more genetic alterations within the TSH-1 locus significantly contribute to the altered thyroid function tests of the WKY rat.
This article has been cited by other articles:
![]() |
L. C. Moeller, M. Alonso, X. Liao, V. Broach, A. Dumitrescu, J. Van Sande, L. Montanelli, S. Skjei, C. Goodwin, H. Grasberger, et al. Pituitary-Thyroid Setpoint and Thyrotropin Receptor Expression in Consomic Rats Endocrinology, October 1, 2007; 148(10): 4727 - 4733. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. C. Solberg, A. E. Baum, N. Ahmadiyeh, K. Shimomura, R. Li, F. W. Turek, J. S. Takahashi, G. A. Churchill, and E. E. Redei Genetic analysis of the stress-responsive adrenocortical axis Physiol Genomics, November 21, 2006; 27(3): 362 - 369. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Lionikas, D. A. Blizard, G. S. Gerhard, D. J. Vandenbergh, J. T. Stout, G. P. Vogler, G. E. McClearn, and L. Larsson Genetic determinants of weight of fast- and slow-twitch skeletal muscle in 500-day-old mice of the C57BL/6J and DBA/2J lineage Physiol Genomics, April 14, 2005; 21(2): 184 - 192. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |