Plateroti M, Gauthier K, Domon-Dell C, Freund J N, Samarut J, Chassande O
Laboratoire de Biologie Moléculaire et Cellulaire de l'ENS de Lyon, UMR 5665 CNRS, LA 913 INRA, 69364 Lyon Cedex 07, France.
Mol Cell Biol. 2001 Jul;21(14):4761-72. doi: 10.1128/MCB.21.14.4761-4772.2001.
Thyroid hormone is known to participate in the control of intestine maturation at weaning. Its action is mediated by the thyroid hormone nuclear receptors, encoded by the TRalpha and TRbeta genes. Since previous studies have shown that TRbeta plays a minor role in the gut, we focused here our analysis on the TRalpha gene. The TRalpha locus generates the TRalpha1 receptor together with the splicing variant TRalpha2 and the truncated products TRDeltaalpha1 and TRDeltaalpha2, which all lack an intact ligand binding domain. The TRDeltaalpha isoforms are transcribed from an internal promoter located in intron 7, and their distribution is restricted to a few tissues including those of the intestine. In order to define the functions of the different isoforms encoded by the TRalpha locus in the intestinal mucosa, we produced mice either lacking all known TRalpha products or harboring a mutation which inactivates the intronic promoter. We performed a detailed analysis of the intestinal phenotypes in these mice and compared it to that of the previously described TRalpha(-/-) mice, in which TRalpha isoforms are abolished but the TRDeltaalpha isoforms remain. This comparative analysis leads us to the following conclusions: (i) the TRalpha1 receptor mediates the T3-dependent functions in the intestine at weaning time and (ii) the TRDeltaalpha products negatively control the responsiveness of the epithelial cells to T3. Moreover, we show that TRDeltaalpha proteins can interfere with the transcription of the intestine-specific homeobox genes cdx1 and cdx2 and that their activity is regulated by TRalpha1. Altogether these data demonstrate that cooperation of TRalpha and TRDeltaalpha products is essential to ensure the normal postnatal development of the intestine and that mutations in the TRalpha locus can generate different phenotypes caused by the disruption of the equilibrium between these products.
已知甲状腺激素参与断奶时肠道成熟的调控。其作用由甲状腺激素核受体介导,该受体由TRα和TRβ基因编码。由于先前的研究表明TRβ在肠道中作用较小,我们在此将分析重点放在TRα基因上。TRα基因座产生TRα1受体以及剪接变体TRα2和截短产物TRΔα1和TRΔα2,它们都缺乏完整的配体结合域。TRΔα同工型从位于内含子7中的内部启动子转录而来,其分布仅限于包括肠道组织在内的少数组织。为了确定TRα基因座编码的不同同工型在肠黏膜中的功能,我们制备了要么缺乏所有已知TRα产物,要么携带使内含子启动子失活的突变的小鼠。我们对这些小鼠的肠道表型进行了详细分析,并将其与先前描述的TRα(-/-)小鼠的表型进行比较,在TRα(-/-)小鼠中TRα同工型被消除,但TRΔα同工型仍然存在。这种比较分析使我们得出以下结论:(i)TRα1受体在断奶时介导肠道中T3依赖的功能,(ii)TRΔα产物负向控制上皮细胞对T3的反应性。此外,我们表明TRΔα蛋白可干扰肠道特异性同源盒基因cdx1和cdx2的转录,并且它们的活性受TRα1调节。总之,这些数据表明TRα和TRΔα产物的协同作用对于确保肠道出生后的正常发育至关重要,并且TRα基因座中的突变可产生由这些产物之间平衡破坏引起的不同表型。