Lazar M A, Chin W W
Department of Medicine Brigham and Women's Hospital, Boston, Massachusetts 02115.
Mol Endocrinol. 1988 Jun;2(6):479-84. doi: 10.1210/mend-2-6-479.
There is recent evidence suggesting that c-erbA is the thyroid hormone nuclear receptor, and that there may be multiple c-erbA genes. We investigated the effect of T3 on two c-erbA mRNAs present in GH3 cells. A partial cDNA was isolated from rat GH3 cells which is nearly identical (99.6% nucleotide identity) to rat c-erbA alpha, except for a unique 3'-region corresponding to the carboxyl terminal region of the predicted protein sequence. This cDNA (c-erbA alpha-2), like rat c-erbA alpha, hybridizes to a 2.6 kilobase (kb) mRNA which is distinct from a 6.2 kb species that hybridizes to c-erbA beta. Since nuclear T3-binding is down-regulated by T3, we hypothesized that one or both c-erbA mRNAs might be regulated by T3. GH3 cells were treated with 10 nM T3 for up to 24 h, a manipulation known to decrease nuclear T3 binding by approximately 2-fold in GH cells. Both the 6.2 kb and 2.6 kb mRNA species decreased to nearly 50% of control values at 24 h. These data indicate that these two c-erbA mRNAs are regulated by T3 and suggest that the T3 effect on T3 binding-activity in GH cells may be mediated, in part, by down-regulation of c-erbA mRNA levels.
最近有证据表明,c-erbA是甲状腺激素核受体,而且可能存在多个c-erbA基因。我们研究了T3对GH3细胞中存在的两种c-erbA mRNA的影响。从大鼠GH3细胞中分离出一个部分cDNA,它与大鼠c-erbAα几乎完全相同(核苷酸同一性为99.6%),只是在对应于预测蛋白质序列羧基末端区域的独特3'-区域有所不同。这个cDNA(c-erbAα-2),与大鼠c-erbAα一样,与一个2.6千碱基(kb)的mRNA杂交,该mRNA与与c-erbAβ杂交的6.2 kb的mRNA不同。由于核T3结合被T3下调,我们推测一种或两种c-erbA mRNA可能受T3调控。用10 nM T3处理GH3细胞长达24小时,这种处理已知会使GH细胞中的核T3结合减少约2倍。在24小时时,6.2 kb和2.6 kb的mRNA种类均降至对照值的近50%。这些数据表明这两种c-erbA mRNA受T3调控,并提示T3对GH细胞中T3结合活性的影响可能部分是由c-erbA mRNA水平的下调介导的。