A peculiar mutation in the DNA-binding/dimerization domain of NFIX causes Sotos-like overgrowth syndrome: A new case

被引:27
作者
Priolo, Manuela [1 ]
Grosso, Enrico [2 ]
Mammi, Corrado [1 ]
Labate, Claudia [1 ]
Naretto, Valeria Giorgia [2 ]
Vacalebre, Caterina [1 ]
Caridi, Paola [1 ]
Lagana, Carmelo [1 ]
机构
[1] Azienda Osped Bianchi Melacrino Morelli, Unita Operat Genet Med, Reggio Di Calabria, Italy
[2] Azienda Osped Univ S Giovanni Battista Torino, SCDU Genet Med, Turin, Italy
关键词
DNA-binding/dimerization domain; NFIX; MH1; domain; Deletion; Sotos-like overgrowth syndrome; MARSHALL-SMITH-SYNDROME; NATURAL-HISTORY; BINDING DOMAIN;
D O I
10.1016/j.gene.2012.08.040
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Nuclear Factor I-X (NFIX) is a member of the nuclear factor I (NFI) family proteins, which are implicated as site-specific DNA-binding proteins and is deleted or mutated in a subset of patients with Sotos-like overgrowth syndrome and in patients with Marshall-Smith syndrome. We evaluated an additional patient with clinical features of Sotos-like syndrome by sequencing analysis of the NFIX gene and identified a 21 nucleotide in frame deletion predicting loss of 7 amino acids in the DNA-binding/dimerization domain of the NFIX protein. The deleted residues are all evolutionally conserved amino acids. The present report further confirms that mutations in DNA-binding/dimerization domain cause haploinsufficiency of the NFIX protein and strongly suggests that in individuals with Sotos-like features unrelated to NSD1 changes genetic testing of NFIX should be considered. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 105
页数:3
相关论文
共 14 条
[1]   Marshall-Smith syndrome: Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities [J].
Adam, MP ;
Hennekam, RCM ;
Keppen, LD ;
Bull, MJ ;
Clericuzio, CL ;
Burke, LW ;
Ormond, KE ;
Hoyme, HE .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 137A (02) :117-124
[2]  
Dekker J, 1996, MOL CELL BIOL, V16, P4073
[3]   Functional mapping of the MH1 DNA-binding domain of DPC4/SMAD4 [J].
Jones, JB ;
Kern, SE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (12) :2363-2368
[4]   A Clinical Study of Sotos Syndrome Patients With Review of the Literature [J].
Leventopoulos, George ;
Kitsiou-Tzeli, Sophia ;
Kritikos, Konstantinos ;
Psoni, Stavroula ;
Mavrou, Ariadni ;
Kanavakis, Emmanuel ;
Fryssira, Helen .
PEDIATRIC NEUROLOGY, 2009, 40 (05) :357-364
[5]   Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome [J].
Malan, Valerie ;
Rajan, Diana ;
Thomas, Sophie ;
Shaw, Adam C. ;
Picard, Helene Louis Dit ;
Layet, Valerie ;
Till, Marianne ;
van Haeringen, Arie ;
Mortier, Geert ;
Nampoothiri, Sheela ;
Puseljic, Silvija ;
Legeai-Mallet, Laurence ;
Carter, Nigel P. ;
Vekemans, Michel ;
Munnich, Arnold ;
Hennekam, Raoul C. ;
Colleaux, Laurence ;
Cormier-Daire, Valerie .
AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 87 (02) :189-198
[6]  
Neri G, 1998, AM J MED GENET, V79, P279, DOI 10.1002/(SICI)1096-8628(19981002)79:4<279::AID-AJMG9>3.0.CO
[7]  
2-H
[8]   Expression, DNA-binding specificity and transcriptional regulation of nuclear factor 1 family proteins from rat [J].
Osada, S ;
Matsubara, T ;
Daimon, S ;
Terazu, Y ;
Xu, MX ;
Nishihara, T ;
Imagawa, M .
BIOCHEMICAL JOURNAL, 1999, 342 :189-198
[9]   Phenotype and Natural History in Marshall-Smith Syndrome [J].
Shaw, Adam C. ;
van Balkom, Inge D. C. ;
Bauer, Mislen ;
Cole, Trevor R. P. ;
Delrue, Marie-Ange ;
Van Haeringen, Arie ;
Holmberg, Eva ;
Knight, Samantha J. L. ;
Mortier, Geert ;
Nampoothiri, Sheela ;
Puseljic, Silvija ;
Zenker, Martin ;
Cormier-Daire, Valerie ;
Hennekam, Raoul C. M. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (11) :2714-2726
[10]   Relationship between the DNA binding domains of SMAD and NFI/CTF transcription factors defines a new superfamily of genes [J].
Stefancsik, R ;
Sarkar, S .
DNA SEQUENCE, 2003, 14 (04) :233-239