Figure 1.
Methylation analysis of the H19-DMR, using bisulfite-treated genomic DNA.
A. Schematic representation of a segment encompassing 21 CpG dinucleotides (CG1→CG21) within the H19-DMR. The cytosine residues at the CpG dinucleotides are usually methylated after paternal transmission (filled circles) and unmethylated after maternal transmission (open circles). The CTCF binding site 6 (CTCF6) is indicated with a blue rectangle; the cytosine residue at CG8 constitutes a C/T SNP (indicated with a gray rectangle). For pyrosequencing analysis, a 279 bp segment was PCR-amplified with PyF & PyR primers, and a sequence primer (SP) was hybridized to a single-stranded PCR products. Subsequently, the MIs were obtained for four CpG dinucleotides (CG5–CG7 and CG9) (indicated with a yellow rectangle). For COBRA, a 435 bp region was PCR-amplified with CoF & CoR primers, and the PCR product was digested with methylated allele-specific restriction enzymes to examine the methylation pattern of CG5 ands CG16 (the PCR products is digested with Hpy188I when the cytosine residue at CG5 is methylated and with AflIII when the cytosine residue at CG16 is methylated) (indicated with orange rectangles). IGF2 is a paternally expressed gene, and H19 is a maternally expressed gene. The stippled ellipse indicates the enhancer for IGF2 and H19. B. Pyrosequencing data. Left part: Representative results indicating the MIs for CG5– CG7 and CG9. CG5– CG7 and CG9 are hypomethylated in case 1, and similarly methylated between case 53 and a control subject. Right part: Histograms showing the distribution of the MIs (the horizontal axis: the methylation index; and the vertical axis: the patient number). Forty-three SRS patients with low MIs are shown in red. C. COBRA data. Left part: Representative findings of PCR products loaded onto a DNA 1000 LabChip (Agilent, Santa Clara, CA, USA) after digestion with Hpy188I or AflIII. U: unmethylated clone specific bands; M: methylated clone specific bands; and BWS: Beckwith-Wiedemann syndrome patient with upd(11p15)pat. Right part: Histograms showing the distribution of the MIs.
Figure 2.
Methylated and unmethylated allele-specific PCR analysis for the MEST-DMR.
A. Schematic representation of the MEST-DMR. The cytosine residues at the CpG dinucleotides are usually unmethylated after paternal transmission (open circles) and methylated after maternal transmission (filled circles). The PCR primers have been designed to hybridize either methylated or unmethylated clones. B. The results of methylation analysis with methylated and unmethylated allele-specific primers.
Table 1.
The methylation indices (%) for the H19-DMR.
Figure 3.
Analysis of the ARHI-DMR in case 13.
For bisulfite sequencing, each line indicates a single clone, and each circle denotes a CpG dinucleotide; the cytosine residues at the CpG dinucleotides are usually unmethylated after paternal transmission (open circles) and methylated after maternal transmission (filled circles). Electrochromatograms delineate the sequences of the primer binding sites utilized for the methylation analysis.
Figure 4.
Oligonucleotide array CGH in case 73, showing a ∼3.86 Mb deletion at chromosome 17q24.
The black, the red, and the green dots denote signals indicative of the normal, the increased(>+0.5), and the decreased (< –1.0) copy numbers, respectively. The horizontal bar with arrowheads indicates a ∼2.3 Mb deletion identified in a patient with Carney complex and SRS-like phenotype [44], and the black square represent a ∼65 kb segment harboring the breakpoint of a de novo translocation 46,XY,t(1;17)(q24;q23–q24) identified in a patient with SRS phenotype [45], [46].
Table 2.
Phenotypic comparison in three groups of patients with Silver-Russell syndrome.
Table 3.
Correlation analyses in patients with H19-DMR hypomethylations.