Pendrin Is a Novel In Vivo Downstream Target Gene of the TTF-1/Nkx-2.1 Homeodomain Transcription Factor in Differentiated Thyroid Cells

Author:

Dentice Monica1,Luongo Cristina2,Elefante Antonia2,Ambrosio Raffaele2,Salzano Salvatore3,Zannini Mariastella13,Nitsch Roberto13,Di Lauro Roberto1,Rossi Guido1,Fenzi Gianfranco2,Salvatore Domenico2

Affiliation:

1. Dipartimento di Biologia e Patologia Cellulare e Molecolare

2. Dipartimento di Endocrinologia ed Oncologia Molecolare e Clinica, Università di Napoli “Federico II,” 80131 Naples, Italy

3. Istituto di Endocrinologia ed Oncologia Sperimentale, CNR-IEOS, 80131 Naples, Italy

Abstract

ABSTRACT Thyroid transcription factor gene 1 ( TTF-1 ) is a homeobox-containing gene involved in thyroid organogenesis. During early thyroid development, the homeobox gene Nkx-2.5 is expressed in thyroid precursor cells coincident with the appearance of TTF-1 . The aim of this study was to investigate the molecular mechanisms underlying thyroid-specific gene expression. We show that the Nkx-2.5 C terminus interacts with the TTF-1 homeodomain and, moreover, that the expression of a dominant-negative Nkx-2.5 isoform (N188K) in thyroid cells reduces TTF-1-driven transcription by titrating TTF-1 away from its target DNA. This process reduced the expression of several thyroid-specific genes, including pendrin and thyroglobulin. Similarly, down-regulation of TTF-1 by RNA interference reduced the expression of both genes, whose promoters are sensitive to and directly associate with TTF-1 in the chromatin context. In conclusion, we demonstrate that pendrin and thyroglobulin are downstream targets in vivo of TTF-1 , whose action is a prime factor in controlling thyroid differentiation in vivo.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

Reference57 articles.

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