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
Centro de Estudos do Genoma Humano e Células Tronco, Departamento de Genética e Biologia Evolutiva, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil.
North East Thames Genetics Service, Great Ormond Street Hospital, London, United Kingdom.
Front Genet. 2018 Apr 25;9:149. doi: 10.3389/fgene.2018.00149. eCollection 2018.
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.
编码区和非编码区的重复序列越来越多地与许多人类遗传疾病相关,如里氏-科斯塔-佩雷拉综合征(RCPS)。RCPS主要特征为下颌骨中线裂、罗宾序列和肢体缺陷,是一种常染色体隐性遗传性肢端颜面发育不全症,主要在巴西患者中报道。这种疾病是由于[具体基因名称]水平降低所致,主要原因是5'非翻译区(5'UTR)重复序列数量增加。5'UTR等位基因富含CG,三种基序的大小和组织方式各不相同。在受影响个体中鉴定出一种独特的等位基因模式,其中CGCA基序最为普遍,在此称为“疾病相关CGCA - 20nt基序”。迄今为止,含有疾病相关基序的致病等位基因的起源以及5'UTR基序对[基因名称]表达的功能影响完全未知。在此,我们对380名未受影响个体的队列中的43种不同的5'UTR等位基因进行了特征分析。我们鉴定出8名携带疾病相关CGCA - 20nt基序的杂合未受影响个体,我们的单倍型分析表明与RCPS相关的单倍型不止一种。对数量、基序组织和单倍型多样性的综合分析,以及观察到与疾病相关CGCA - 20nt基序相关的两种明显不同的单倍型,表明RCPS等位基因可能至少两次起源于古代等位基因之间独立的不等交换事件。此外,我们已经表明5'UTR区域中基序的数量和序列与[基因名称]抑制相关,这不是由CpG甲基化介导的。总之,本研究表明[基因名称]中的大量重复序列并不代表动态突变,并且RCPS可出现在任何携带CGCA -