Complexity of the 5' Untranslated Region of EIF4A3 , a Critical Factor for Craniofacial and Neural Development

• Published in: Frontiers in genetics 2018-04, Vol.9, p.149-149
• Main Authors: Hsia, Gabriella S P, Musso, Camila M, Alvizi, Lucas, Brito, Luciano A, Kobayashi, Gerson S, Pavanello, Rita C M, Zatz, Mayana, Gardham, Alice, Wakeling, Emma, Zechi-Ceide, Roseli M, Bertola, Debora, Passos-Bueno, Maria Rita
• Format: Article
• Language: English
• Subjects: acrofacial dysostosis; crossing-over; expansion; Genetics; haplotype; non-coding region
• ISSN: 1664-8021; 1664-8021
• DOI: 10.3389/fgene.2018.00149

Repeats in coding and non-coding regions have increasingly been associated with many human genetic disorders, such as Richieri-Costa-Pereira syndrome (RCPS). RCPS, mostly characterized by midline cleft mandible, Robin sequence and limb defects, is an autosomal-recessive acrofacial dysostosis mainly reported in Brazilian patients. This disorder is caused by decreased levels of , mostly due to an increased number of repeats at the 5'UTR. 5'UTR alleles are CG-rich and vary in size and organization of three types of motifs. An exclusive allelic pattern was identified among affected individuals, in which the CGCA-motif is the most prevalent, herein referred as "disease-associated CGCA-20nt motif." The origin of the pathogenic alleles containing the disease-associated motif, as well as the functional effects of the 5'UTR motifs on expression, to date, are entirely unknown. Here, we characterized 43 different 5'UTR alleles in a cohort of 380 unaffected individuals. We identified eight heterozygous unaffected individuals harboring the disease-associated CGCA-20nt motif and our haplotype analyses indicate that there are more than one haplotype associated with RCPS. The combined analysis of number, motif organization and haplotypic diversity, as well as the observation of two apparently distinct haplotypes associated with the disease-associated CGCA-20nt motif, suggest that the RCPS alleles might have arisen from independent unequal crossing-over events between ancient alleles at least twice. Moreover, we have shown that the number and sequence of motifs in the 5'UTR region is associated with repression, which is not mediated by CpG methylation. In conclusion, this study has shown that the large number of repeats in does not represent a dynamic mutation and RCPS can arise in any population harboring alleles with the CGCA-20nt motif. We also provided further evidence that 5'UTR is a regulatory region and the size and sequence type of the repeats at 5'UTR may contribute to clinical variability in RCPS.