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Am J Med Genet A. Author manuscript; available in PMC 2010 October 1.
Published in final edited form as:
PMCID: PMC2768228
NIHMSID: NIHMS135012

Genomic Duplication of PTPN11 is an Uncommon Cause of Noonan Syndrome

Abstract

Noonan syndrome (NS) is a genetically heterogeneous disorder caused most commonly by activating mutations in PTPN11. We report a patient with hypotonia, developmental delay and clinical features suggestive of NS. High-resolution chromosome analysis was normal, and sequence analyses of PTPN11, SOS1, KRAS, BRAF, RAF1, MEK, and MEK2 were also normal. Array CGH revealed a single copy gain of 9 BAC clones at 12q24.11q24.21 (8.98 Mb in size), which encompassed the PTPN11 locus at 12q24.13 and was confirmed by FISH analysis. Shchelochkov et al., [2008] reported a similar case and speculated that such duplications might account for 15–30% of NS cases with no detectable mutation in NS genes. We screened more than 250 NS cases without mutation in known NS disease-causing genes by quantitative PCR, and none of these studies produced results in the duplicated range. We also explored the possibility that de novo changes affecting the untranslated region (UTR) of the PTPN11 transcript might represent an alternative event involved in SHP2 enhanced expression. DHPLC analysis and direct sequencing of the entire 3' UTR in 36 NS patients without mutation in known genes did not show any disease-associated variant. These findings indicate that duplications of PTPN11 represent an uncommon cause of NS, and functionally relevant variations within the 3'UTR of the gene do not appear to play a major role in NS. However, recurrent observations of NS in individuals with duplications involving the PTPN11 locus suggest that increased dosage of SHP2 may have dysregulating effects on intracellular signaling.

Keywords: Noonan syndrome, PTPN11, TBX3, TBX5, Gene Duplication PTPN11, Array CGH, Duplication 12q24.3, Dosage Sensitive Gene

INTRODUCTION

Noonan syndrome (NS) is a relatively common autosomal dominant condition, which may be sporadic or inherited [Noonan, 2006; Allanson 2007]. It consists of characteristic facial features, short stature, heart defects, particularly pulmonic stenosis, developmental delay in about one third of cases (usually preceded by failure to thrive), blood clotting disorders, variable ectodermal involvement, and susceptibility to certain cancers, particularly juvenile monomyelocytic leukemia (JMML). Dermatologic findings may include café-au-lait spots, keratosis pilaris, lentigines, and nevi. NS may be caused by gain of function mutations in PTPN11 (50%), which encodes SHP2, a protein tyrosine phosphatase with positive modulatory role in RAS-MAPK signaling, or functional dysregulation of other signal transducers participating in this signal cascade, including, SOS1, KRAS, RAF1 or BRAF [Tartaglia et. al. 2001; Zenker et al.,, 2004; Schubbert et al 2006; Roberts et al 2007; Tartaglia et al., 2007; Nava et al.,, 2007; Razzaque et al 2007; Pandit et al 2007; Sarkozy et al.,, 2009]. Overall, mutations in identified genes account for approximately 70–75% of affected cases, indicating that other disease-causing events remain to be identified.

We report on the identification of a de novo duplication of 8.98 Mb at 12q24.11q24.21, encompassing PTPN11, in a 4-year-old male with a phenotype fitting NS, apparently normal chromosomes and no mutation in known disease genes. Quantitative PCR analysis and denaturing high-performance liquid chromatography (DHPLC) screening performed to explore prevalence of PTPN11 copy number gain and functionally relevant changes in the 3' untranslated region (UTR) of PTPN11 support the view that duplications of PTPN11 are uncommon as a cause of NS and that functionally relevant 3'UTR variants do not appear to be associated significantly with this disorder.

CLINICAL REPORT

The patient was the AGA term product of an uncomplicated pregnancy, labor and delivery, born to a 28-year-old primigravida mother and a 27-year-old father. After her second pregnancy, in retrospect, his mother noted that the fetal movements of her first pregnancy were less vigorous than in her second pregnancy. His delivery was via cesarean for failure to progress. Family history was non-contributory, and he was born weighing 3.72 kg, and measuring 53 cm in length, with a head circumference of 36 cm. Pyloric stenosis was detected and repaired at age 4 weeks, and he underwent inguinal hernia repair with orchiopexy at age 4 months. Feeding difficulties remained evident after birth, and a lingual frenulum was clipped. He continued to have poor postnatal growth about 2 SD below mean for age with preservation of his head size at the 50thcentile. He was a very slow feeder, with a weak suck, and he seldom took more than 100 cc of feeding at a time. He was delayed in transitioning to solid foods. Motor milestones were delayed during infancy, and he was referred for early intervention to developmental services at age 1 year because he was not crawling. A neurologist noted generalized hypotonia, and thyroid studies and pediatric eye evaluation were normal. He had recurrent ear infections requiring insertion of pressure-equalizing tubes and adenoidectomy. Echocardiogram revealed only mild mitral valve regurgitation. His coagulation parameters were normal.

His skin appeared thin and smooth with easy bruising and several faint café au lait macules. His hair was thin and fine, and he had a prominent forehead with down-slanting palpebral fissures, bilateral epicanthal folds, and a flat nasal bridge (Fig 1). He had full lips, an upturned nasal tip, and a short, wide neck. He had hypoplastic nipples and mild pectus deformity with superior pectus carinatum and inferior pectus excavatum. He had bilateral single transverse palmar flexion creases and flat feet, and his joints were very loose, especially in his hands and feet. He had generalized hypotonia with normal hearing, with mildly delayed social skills, fine and gross motor skills and expressive language skills. Formal developmental assessment at age 29 months placed his cognitive skills at 23–25 months, social skills at 25 months, fine motor skills at 18–23 months, and self-help skills at 29 months. At 33 months, his gross motor skills were at 22–26 months, and at age 4 years his auditory comprehension skills were at 3.1 years, with expressive communication skills at 2.7 years. His height was 84.5 cm (just under the 3rd centile), weight 11.6 kg (3rd centile), head circumference 50.5 cm (50th centile).

Figure 1
Clinical features of the patient at ages 25 months and 45 months (top left and right) illustrating facial features for Noonan syndrome along with typical pectus deformity.

METHODS

Patient cohorts

As a collaborative multicentric effort, 250 subjects with NS or a phenotype suggestive of this condition were screened to explore prevalence of PTPN11 copy number gains. Clinical features for 124 of these subjects satisfied diagnostic criteria reported by van der Burgt et al. [1994], while another 53 cases were more atypical, most of them displaying variable cognitive deficits and developmental delay as well as additional anomalies compatible with NS. These patients had been evaluated by experienced clinicians either personally or by reviewing history, documented clinical findings and photographs. The remaining 73 subjects of this cohort were referred for mutation analysis by clinicians who suspected a diagnosis of NS. None of the subjects carried a mutation in the PTPN11, SOS, KRAS, or RAF1 gene based on scanning of the coding exons by denaturing high-performance liquid chromatography (DHPLC) analysis and/or direct sequencing.

Scanning of the 3' UTR of the PTPN11 gene was performed on a subgroup of 36 subjects with clinical features that satisfied NS diagnostic criteria (see above). None of the subjects carried a mutation in the PTPN11, SOS, KRAS, RAF1, MEK1 or MEK2 genes.

Array CGH Analysis and FISH Analysis

Array CGH was performed with a BAC microarray (the SignatureChip®-www.signaturegenomics.com) that was developed for the detection of microdeletions, microduplications, aneuploidy, unbalanced translocations, and subtelomeric and pericentromeric copy-number alterations [Bejjani et al., 2005]. As shown in Figure 2, microarray analysis was performed and analyzed as described [Bejjani et al., 2005], and with an oligonucleotide array (the SignatureChipOS®) as described [Ballif et al., 2008]. All abnormalities detected by array CGH were confirmed by fluorescence in situ hybridization (FISH) as published [Shaffer et al., 1994] using a BAC clone from the PTPN11 locus (RP11–9P8), revealing a duplication at 12q24.13 visible on metaphase chromosomes. The centromere probe to chromosome 12 was use as a control and showed a normal hybridization pattern.

Figure 2
PTPN11 single copy gain in the patient with clinical features fitting NS. Array CGH analysis demonstrated a single-copy gain of nine BAC clones at 12q24.11q24.21 (centromeric RP1-46F2, RP11-124I12, RP11-767G4, RP11-421J14, RP11-9P8, RP5-1048I22, RP11-438N16, ...

Quantitative PCR

Quantitative real-time PCR analysis for PTPN11 exon 5 and exon 9 was performed using custom designed primers and TaqMan minor-groove binder probes according to the manufacturer's recommendations with the PrimerExpress 2.0 Software (Applied Biosystems, Foster City, USA) from the Genbank sequence NM_002834 (PTPN11 exon 5: forward primer 5'-GTGGAGGAGAACGGTTTGATTC-3', reverse primer 5'-CCAATGTTTCCACCATAGGATTC-3', probe 6FAM-AGATCTTGTGGAACATTATA. PTPN11 exon 9: forward primer: 5'-GAATTTGAAACCAAGTGCAACAAT-3', 5'-CAGCCTTGTGTGGCAATGTAA-3', probe 6FAM-CAAAGCCCAAAAAG). The assay for each sample was performed in 384-well plates with a final volume of 20 μl on an ABI 7900HT in a multiplex reaction with the endogenous control of albumin exon 12 as described previously [Thiel et al., 2003]. Copy number levels were calculated using the ΔΔCt method and normalized to the expression levels of healthy control samples.

Mutation analysis

The entire coding sequence and flanking intronic portions of the PTPN11 gene were screened by direct sequencing using the ABI BigDye terminator Sequencing Kit v.1.1 (Applied Biosystem, Foster City, CA) and an ABI 3700 Capillary Array Sequencer). Exclusion of mutations within the affected exons of SOS1, KRAS, BRAF, RAF1, MEK1, and MEK2 as well as of disease-associated sequence variants within the 3' UTR of the PTPN11 gene was based on DHPLC (3100 and 3500HT WAVE DNA fragment analysis systems, Transgenomic) scanning. Amplimers having abnormal denaturing profiles were purified (Microcon PCR, Millipore) and sequenced bi-directionally. Primer pairs, and PCR and DHPLC analysis settings are available upon request.

RESULTS

Initial high resolution chromosome analysis revealed a normal male karyotype. After PTPN11 was sequenced and found to be normal, array CGH was performed because of the child's hypotonia and developmental delay. This assay demonstrated a single copy gain of 9 BAC clones at 12q24.11q24.21 (Figure 2), which included the PTPN11 locus, as well as TBX3 and TBX5. This finding was confirmed by FISH analysis (Fig 2). Informed consent was obtained from the family to analyze the other NS causative genes on a research basis. An additional array CGH analysis was performed on an oligonucleotide array and further defined the extent of duplication to be 8.98 Mb. The genomic coordinates of the duplication on 12q24.3 were determined to be: 104,641,698– 113,603,100. The child's DNA was also used as reference to check for changes in PTPN11 copy number in a cohort of 250 subjects with NS or a phenotype suggestive of this disorder without mutations in known NS disease-causing genes by qPCR. We did not observe any duplication, indicating that PTPN11 gene duplication is not a frequent event among subjects with this disorder. We explored the possibility that de novo changes affecting the 3' untranslated sequence of the PTPN11 transcript might represent an alternative mechanism involved in SHP2 dysregulated expression. DHPLC screening and direct sequencing performed on 36 subjects with NS without mutation in known genes did not reveal any disease-associated variant.

DISCUSSION

NS is a genetically heterogeneous disorder that may be caused by gain of function mutations in PTPN11 (50%) or other genes coding for proteins participating in the RAS-MAPK pathway, including SOS1 (15–20%), KRAS (2%), or RAF1 (5–10%) or BRAF (2%) [Sarkozy et al., 2009; Tartaglia and Gelb, 2009]. The molecular cause underlying this disorder is still unknown in approximately 25–30% of affected individuals. NS-causing PTPN11 mutations generally promote upregulation of SHP-2 function and enhanced signal flow through RAS [Tartaglia and Gelb, 2009]. Most mutations affect amino acid residues participating in stabilization of the N-SH2/PTP domain interaction that maintains SHP-2 in its catalytically active conformation, but other mechanisms appear to be also involved [Keilhack et al., 2005; Tartaglia et al., 2006; Martinelli et al., 2008]. While it has been established that a different group of PTPN11 mutations is acquired as a somatic event in childhood acute leukemias and myeloproliferative or myelodysplastic disorders [Tartaglia et al., 2003; 2004], a study documented an alternative perturbing effect of SHP-2 on signaling and leukemogenesis via enhanced espression [Xu et al., 2005]. This observation raised the hypothesis that PTPN11 gene duplication/amplification might affect developmental processes via gene dosage effect. Consistently, a dosage effect for a mutated PTPN11 gene has been documented in mice [Araki et al., 2004] and humans [Becker et al., 2007].

In our patient with NS clinical features, no mutation was found in the PTPN11, KRAS, SOS1, RAF1, BRAF, MEK1 and MEK2 genes, while array-CGH demonstrated an 8.98 Mb duplication at 12q24.3, which included the PTPN11 locus. A similar finding was recently documented by Shchelochkov et al. [2008] who reported a 3-year-old girl with a similar duplication that also included PTPN11. This patient had hypotonia, coarctation of the aorta, ASD and VSD (closed spontaneously), velopharyngeal incompetence, hypertelorism, ptosis, epicanthal folds, cupped ears, microcephaly, pectus excavatum and short stature (10th centile) with developmental delay. Based on this finding and available records, these authors suggested that PTPN11 duplication might be a common cause for NS due to increased gene dosage.

There are several other reports of patients with duplications of 12q24 encompassing PTPN11 [Harrod et al., 1980; Dixon et al., 1993; Doco-Fenzy et al., 2006; Cappellacci et al., 2007]. Only the patient reported herein and the patients reported by Doco-Fenzy et al. [2006] and Shchelochkov et al. [2008] were initially suspected of having NS, and these other two reported patients had microcephaly and aortic anomalies. Many of their other manifestations are seen in NS, such as failure to thrive, developmental delay, short neck, wide spaced nipples, chest deformity, and minor facial anomalies such as hypertelorism, small chin, and down-turned corners of the mouth. The duplication observed in all 3 of these patients who were initially suspected of having NS also includes TBX3 and TBX5, whose action may be dosage-sensitive. Overexpression of TBX5 is known to have an impact on cardiogenesis [Hatcher et al., 2004]. While these data suggest that duplications of the region containing PTPN11 might result in an enhanced expression level of SHP2 that could have activating effects on intracellular signaling similar to a mutant SHP2 protein with dysregulated function and may affect development, our findings support the view that PTPN11 duplication does not represent a common cause of this disorder. Since our qPCR screening was performed using two intragenic fragment only (exons 5 and 11), we however cannot rule out the hypothesis that smaller intragenic in-frame duplications or deletions affecting PTPN11 might upregulate SHP2 function and cause NS or a related phenotype.

Figure 3
PTPN11 gene duplication does not represent a major event in NS. Quantitative real-time PCR analysis was used to check for changes in PTPN11 copy number in a cohort of 250 NS cases without a mutation in known NS disease-causing genes. Two coding regions ...

Supplementary Material

Supp Data

ACKNOWLEDGMENTS

We appreciate support from SHARE's Childhood Disability Center, the Steven Spielberg Pediatric Research Center, and the NIH/NICHD Program Project Grant (HD22657 to JMG), Medical Genetics NIH/NIGMS Training Program Grant (5-T32-GM08243 to JMG), Telethon-Italy Grant (GGP07115 to MT), “Collaborazione Italia-USA/malattie rare 2007/2009” Grant (to MT), and the German Research Foundation (DFG; ZE 524/4–1 to MZ). We also appreciate assistance from the Cedars-Sinai General Clinical Research Center Grant (M01-RR00425) for samples collected under CSMC IRB Protocols 0463 and 4232.

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