| Literature DB >> 27633570 |
Keiko Shimojima1, Satoshi Narai2, Masami Togawa2, Tomotsune Doumoto2, Noriko Sangu3, Olivier M Vanakker4, Anne de Paepe4, Matthew Edwards5, John Whitehall5, Sally Brescianini6, Florence Petit7, Joris Andrieux8, Toshiyuki Yamamoto9.
Abstract
There are no published reports of patients harboring microdeletions involving the 7p22.1 region. Although 7p22.1 microdeletions are rare, some reports have shown microduplications encompassing this region. In this study, we report five patients with overlapping deletions of the 7p22.1 region. The patients exhibited clinical similarities including non-specific developmental delay, short stature, microcephaly, and other distinctive features. The shortest region of overlap within the 7p22.1 region includes five genes, FBXL18, ACTB, FSCN1, RNF216, and ZNF815P. Of these genes, only ACTB is known to be associated with an autosomal dominant trait. Dominant negative mutations in ACTB are responsible for Baraitser-Winter syndrome 1. We analyzed ACTB expression in immortalized lymphocytes derived from one of the patients and found that it was reduced to approximately half that observed in controls. This indicates that ACTB expression is linearly correlated with the gene copy number. We suggest that haploinsufficiency of ACTB may be responsible for the clinical features of patients with 7p22.1 microdeletions.Entities:
Keywords: 7p22.1 microdeletion; Baraitser-Winter syndrome 1 (BRWS1); Developmental delay; Microcephaly; Short stature; The beta-actin gene (ACTB)
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Year: 2016 PMID: 27633570 DOI: 10.1016/j.ejmg.2016.09.008
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708