A pedigree of a five-generation multinodular goitre family.

<p>Individuals are numbered above each symbol. Individuals affected with MNG are indicated by filled symbols and age of onset is described under the patient symbol. The arrow shows a proband of this family study. The bars above each symbol indicate individuals included in the linkage analysis.</p

Novel variants identified in the proband in the chromosome 19 linkage region.

<p>ref.: reference sequence.</p

Up-regulation of NFE2L2 target genes in the thyroid tissues of the patient.

<p>Results of the quantitative PCR of <i>NFE2L2</i> and its target genes <i>GSTA4</i>, <i>GCLC</i> and <i>NQO1</i> in the normal and goitre region of thyroid tissues obtained from the proband. The expression levels relative to control RNA from an adult thyroid are shown. The significance with the t-test is indicated with asterisks (*p<0.05 and **p<0.01).</p

Reverse transcriptase-PCR for mutant and wild type <b><i>KEAP1</i></b><b>.</b>

<p>(A) Primer positions for reverse transcriptase-PCR in KEAP1 exons. The asterisk indicates the position of c.879_880delinsA mutation in exon 3. The primer, KEAP1-mut-rvs, contains "T" nucleotide at the 3' end which is the complement of mutant "A" nucleotide to amplify mutant allele. The expected sizes of PCR products are as follows: 233 bp for KEAP1-N-fwd and KEAP1-N-rvs; 201 bp for KEAP1-C-fwd and KEAP1-C-rvs; 282 bp for KEAP1-mut-fwd and KEAP1-mut-rvs. (B) Results of the reverse transcriptase-PCR for the mutant and wild type <i>KEAP1</i>. cDNAs from control normal thyroid, the normal and goitre region of thyroid tissues obtained from the proband were amplified by 3 primer sets indicated in (A) to mutant <i>KEAP1</i> (upper panel), 5' and 3' normal portions adjacent mutation site (second and third panels, respectively) of <i>KEAP1</i>. <i>GAPDH</i> was amplified as a control for the amount of cDNA in each sample. The expected size of PCR product of <i>GAPDH</i> is 452 bp. In the experiment of mutant KEAP1 amplification, the plasmids containing mutant or wild type KEAP1 (pCMV-myc-KEAP1mut or pCMV-myc-KEAP1wt, respectively) were utilized as control templates.</p

Identification of a heterozygous mutation in <b><i>KEAP1</i></b><b>.</b>

<p>(A) The result of Sanger sequencing of proband DNA showed the c.879_880delinsA mutation (red), resulting in a 1-base deletion and a frameshift (p.Asp294Thr, fs*23) in <i>KEAP1</i>. (B) Domain structure and mutation location in the KEAP1 protein. The protein consists of an N-terminal region (NTR; amino acids 1 to 60), a BTB domain (amino acids 61 to 179), an intervening region (IVR; amino acids 180 to 314) and a DC domain (amino acids 315 to 624). The BTB and N-terminal portion of IVR is responsible for dimerisation and the interaction with CUL3. The DC domain is also critical for the interaction with NFE2L2. The p.Asp294Thr, fs*23 mutation is located in the IVR. The reported frequencies of the somatic mutations observed in each domain in cancer cells are shown at the bottom <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0065141#pone.0065141-Taguchi1" target="_blank">[32]</a>.</p

Identification of a <i>KEAP1</i> Germline Mutation in a Family with Multinodular Goitre

<div><p>Background</p><p>The familial clustering of multinodular goitres (MNGs) with a dominant mode of inheritance has been repeatedly reported. Linkage studies have revealed several genetic loci responsible for familial MNG; however, most of the causative variants remain unknown.</p> <p>Methods and Results</p><p>Through linkage analysis using single-nucleotide polymorphism markers, we identified a new MNG locus on 19p13.2-q12 in a five-generation Japanese MNG family. Subsequent mutation searches focusing on the candidate 25-Mb region of chromosome 19 identified a heterozygous mutation, c.879_880delinsA, p.Asp294Thr, fs*23, in exon 3 of the <i>KEAP1</i>, which plays a central role in the cytoprotection pathway against oxidative stress. Reverse transcriptase-PCR analysis showed low expression of wild type <i>KEAP1</i> accompanied by no transcription product of mutant allele in the normal and goitre region of thyroid tissues obtained from the proband. In agreement with previous studies showing that KEAP1 negatively regulates NFE2L2, the NFE2L2 target genes <i>GSTA4</i> and <i>GCLC</i> were up-regulated in the thyroid tissues of the patient.</p> <p>Conclusions</p><p>This study identified the first <i>KEAP1</i> mutation in MNG. The results provide insights into the pathogenesis of goitre which develops in the organ continuously exposed to oxidative stress during hormone synthesis.</p> </div

Additional file 3: of In vivo hepatogenic capacity and therapeutic potential of stem cells from human exfoliated deciduous teeth in liver fibrosis in mice

Table S1. Presenting the TaqMan primers and probes used for mouse genes used in real-time PCR, and Table S2 presenting the primer pairs used for human and mouse genes for genomic PCR and RT-PCR. (DOC 65 kb