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
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
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.