The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning.

Abstract

Thyroid dysgenesis is the major cause of congenital hypothyroidism in humans. The underlying molecular mechanism is in most cases unknown, but the frequent co-incidence of cardiac anomalies suggests that the thyroid morphogenetic process may depend on proper cardiovascular development. The T-box transcription factor TBX1, which is the most probable gene for the 22q11 deletion syndrome (22q11DS/DiGeorge syndrome/velo-cardio-facial syndrome), has emerged as a central player in the coordinated formation of organs and tissues derived from the pharyngeal apparatus and the adjacent secondary heart field from which the cardiac outflow tract derives. Here, we show that Tbx1 impacts greatly on the developing thyroid gland, although it cannot be detected in the thyroid primordium at any embryonic stage. Specifically, in Tbx1-/- mice, the downward translocation of Titf1/Nkx2.1-expressing thyroid progenitor cells is much delayed. In late mutant embryos, the thyroid fails to form symmetric lobes but persists as a single mass approximately one-fourth of the normal size. The hypoplastic gland mostly attains a unilateral position resembling thyroid hemiagenesis. The data further suggest that failure of the thyroid primordium to re-establish contact with the aortic sac is a key abnormality preventing normal growth of the midline anlage along the third pharyngeal arch arteries. In normal development, this interaction may be facilitated by Tbx1-expressing mesenchyme filling the gap between the pharyngeal endoderm and the detached thyroid primordium. The findings indicate that Tbx1 regulates intermediate steps of thyroid development by a non-cell-autonomous mechanism. Thyroid dysgenesis related to Tbx1 inactivation may explain an overrepresentation of hypothyroidism occurring in patients with the 22q11DS.

• Authors: H Fagman, J Liao, J Westerlund, L Andersson, B E Morrow, M Nilsson
• Journal: Human molecular genetics (Hum Mol Genet) Vol. 16 Issue 3 Pg. 276-85 (Feb 01 2007) ISSN: 0964-6906 [Print] England
• PMID: 17164259 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• T-Box Domain Proteins
• TBX1 protein, human

Topics

• Animals
• Choristoma (genetics)
• Computer Simulation
• DiGeorge Syndrome (genetics)
• Mesoderm (metabolism)
• Mice
• Mice, Inbred C57BL
• Mice, Knockout
• Models, Biological
• Organ Size
• T-Box Domain Proteins (genetics, metabolism, physiology)
• Thyroid Dysgenesis (embryology, genetics)
• Thyroid Gland (embryology, metabolism, pathology)