SUBSTITUTION OF THE SEAT-BELT REGION OF THE THYROID-STIMULATING HORMONE (TSH) BETA-SUBUNIT WITH THE CORRESPONDING REGIONS OF CHORIOGONADOTROPIN OR FOLLITROPIN CONFERS LUTEOTROPIC BUT NOT FOLLITROPIC ACTIVITY TO CHIMERIC TSH

Citation
M. Grossmann et al., SUBSTITUTION OF THE SEAT-BELT REGION OF THE THYROID-STIMULATING HORMONE (TSH) BETA-SUBUNIT WITH THE CORRESPONDING REGIONS OF CHORIOGONADOTROPIN OR FOLLITROPIN CONFERS LUTEOTROPIC BUT NOT FOLLITROPIC ACTIVITY TO CHIMERIC TSH, The Journal of biological chemistry, 272(24), 1997, pp. 15532-15540
Citations number
36
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
272
Issue
24
Year of publication
1997
Pages
15532 - 15540
Database
ISI
SICI code
0021-9258(1997)272:24<15532:SOTSRO>2.0.ZU;2-J
Abstract
The region between the 10th and 12th cysteine (Cys(88)-Cys(105) in hum an thyroid-stimulating hormone beta-subunit (hTSH beta)) of the glycop rotein hormone beta-subunits corresponds to the disulfide-linked seat- belt region. It wraps around the common alpha-subunit and has been imp licated in regulating specificity between human choriogonado-tropin (h CG) and human follicle-stimulating hormone (hFSH), but determinants of hTSH specificity are unknown, To characterize the role of this region for hTSH, we constructed hTSH chimeras in which the entire seatbelt r egion Cys(88)-Cys(105) or individual intercysteine segments Cys(88)-Cy s(95) and Cys(95)-Cys(105) were replaced with the corresponding sequen ces of hCG and hFSH or alanine cassettes. Alanine cassette mutagenesis of hTSH showed that the Cys(95)-Cys(105) segment of the seat-belt was more important for TSI-I receptor binding and signal transduction tha n the Cys(88)-Cys(95) determinant loop region. Replacing the entire se at-belt of hTSH beta with the hCG sequence conferred full hCG receptor binding and activation to the hTSH chimera, whereas TSI-I receptor bi nding and activation were abolished. Conversely, introduction of the h TSH beta seat-belt sequence into hCG beta generated an hCG chimera tha t bound to and activated the TSH receptor but not the CG/lutropin (LH) receptor. In contrast, an hTSH chimera bearing hFSH seat-belt residue s did not possess any follitropic activity, and its thyrotropic activi ty was only slightly reduced. This may in part be due to the fact that the net charge of the seat-belt is similar in hTSH and hFSH but diffe rent from hCG. However, exchanging other regions of charge heterogenei ty between hTSH beta and hFSH beta did not confer follitropic activity to hTSH. Thus, exchanging the seatbelt region between hTSH and hCG; s witches hormonal specificity in a mutually exclusive fashion, In contr ast, the seat-belt appears not to discriminate between the TSH and the FSH receptors, indicating for the first time that domains outside the seat-belt region contribute to glycoprotein hormone specificity.