de Pontual Loïc, Mathieu Yves, Golzio Christelle, Rio Marlène, Malan Valérie, Boddaert Nathalie, Soufflet Christine, Picard Capucine, Durandy Anne, Dobbie Angus, Heron Delphine, Isidor Bertrand, Motte Jacques, Newburry-Ecob Ruth, Pasquier Laurent, Tardieu Marc, Viot Géraldine, Jaubert Francis, Munnich Arnold, Colleaux Laurence, Vekemans Michel, Etchevers Heather, Lyonnet Stanislas, Amiel Jeanne
Unité INSERM U-781, Université Paris Descartes, Faculté de Médecine, INSERM.
Hum Mutat. 2009 Apr;30(4):669-76. doi: 10.1002/humu.20935.
Pitt-Hopkins syndrome is a severe congenital encephalopathy recently ascribed to de novo heterozygous TCF4 gene mutations. We report a series of 13 novel PHS cases with a TCF4 mutation and show that EEG, brain magnetic resonance imagain (MRI), and immunological investigations provide valuable additional clues to the diagnosis. We confirm a mutational hot spot in the basic domain of the E-protein. Functional studies illustrate that heterodimerisation of mutant TCF4 proteins with a tissue-specific transcription factor is less effective than that homodimerisation in a luciferase reporter assay. We also show that the TCF4 expression pattern in human embryonic development is widespread but not ubiquitous. In summary, we further delineate an underdiagnosed mental retardation syndrome, highlighting TCF4 function during development and facilitating diagnosis within the first year of life.
皮特-霍普金斯综合征是一种严重的先天性脑病,最近被归因于新生的杂合性TCF4基因突变。我们报告了一系列13例携带TCF4突变的新型皮特-霍普金斯综合征病例,并表明脑电图、脑磁共振成像(MRI)和免疫学检查为诊断提供了有价值的额外线索。我们证实了E蛋白碱性结构域中的一个突变热点。功能研究表明,在荧光素酶报告基因检测中,突变型TCF4蛋白与组织特异性转录因子的异源二聚化作用不如同源二聚化有效。我们还表明,TCF4在人类胚胎发育中的表达模式广泛但并非无处不在。总之,我们进一步描述了一种诊断不足的智力发育迟缓综合征,突出了TCF4在发育过程中的功能,并有助于在生命的第一年内进行诊断。