Genotype-phenotype correlation in Brazillian Rett syndrome patients

Correlação genótipo-fenótipo em pacientes brasileiras com síndrome de Rett

Genotype-phenotype correlation in Brazillian Rett syndrome patients

Correlação genótipo-fenótipo em pacientes brasileiras com síndrome de Rett

Fernanda T. de Lima^I; Decio Brunoni^II; José Salomão Schwartzman^III; Maria Cristina Pozzi^IV; Fernando Kok^V; Yara Juliano^VI; Lygia da Veiga Pereira^VII

^IMédica Geneticista Clínico, Doutorado em Ciências, Centro de Genética Médica, Universidade Federal de São Paulo (UNIFESP), São Paulo SP, Brazil

^IIMédico Geneticista Clínico, Livre Docente, Centro de Genética Médica, UNIFESP; Programa de Pós-Graduação em Distúrbios do Desenvolvimento da Universidade Presbiteriana Mackenzie, São Paulo SP, Brazil

^IIIMédico Neuropediatra, Doutorado em Medicina, Programa de Pós-Graduação em Distúrbios do Desenvolvimento da Universidade Presbiteriana Mackenzie, São Paulo SP, Brazil, Associação Brasileira de Síndrome de Rett, São Paulo SP, Brazil

^IVMédica Neuropediatra, Mestrado em Medicina, Associação Brasileira de Síndrome de Rett, São Paulo SP, Brazil

^VMédico Neuropediatra, Pós-doutorado em Medicina, Faculdade de Medicina, Universidade de São Paulo (USP), São Paulo SP, Brazil

^VIAdministradora Hospitalar, Doutorado em Ciências, Professora Titular da Disciplina de Saúde Coletiva da Universidade de Santo Amaro, São Paulo SP, Brasil

^VIIFísica, Doutorado em Ciências Biomédicas, Livre Docente, Laboratório de Genética Molecular, Instituto de Biociências, USP. Financing: IRSA - International Rett Syndrome Association; FADA - Fundo de Auxílio aos Docentes e Alunos da UNIFESP-EPM; CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; FAPESP - Fundação de Amparo a Pesquisa do Estado de São Paulo

ABSTRACT

BACKGROUND: Rett syndrome (RS) is a severe neurodevelopmental X-linked dominant disorder caused by mutations in the MECP2 gene.

PURPOSE: To search for point mutations on the MECP2 gene and to establish a correlation between the main point mutations found and the phenotype.

METHOD: Clinical evaluation of 105 patients, following a standard protocol. Detection of point mutations on the MECP2 gene was performed on peripheral blood DNA by sequencing the coding region of the gene.

RESULTS: Classical RS was seen in 68% of the patients. Pathogenic point mutations were found in 64.1% of all patients and in 70.42% of those with the classical phenotype. Four new sequence variations were found, and their nature suggests patogenicity. Genotype-phenotype correlations were performed.

CONCLUSION: Detailed clinical descriptions and identification of the underlying genetic alterations of this Brazilian RS population add to our knowledge of genotype/phenotype correlations, guiding the implementation of mutation searching programs.

Key words: Rett syndrome, genotype-phenotype correlation.

RESUMO

INTRODUÇÃO: A síndrome de Rett é uma grave doença do neurodesenvolvimento ligada ao X dominante, causada por mutações no gene MECP2.

OBJETIVOS: Identificar mutações de ponto no gene MECP2 e estabelecer uma correlação entre as principais mutações encontradas e o fenótipo.

MÉTODO: Avaliação clínica de 105 pacientes, seguindo um protocolo estabelecido. A identificação de mutações de ponto foi realizada em DNA de sangue periférico por sequenciamento da região codificante do gene amplificada por PCR.

RESULTADOS: Em 68% dos pacientes observou-se o quadro clássico da síndrome. Mutações de ponto patogênicas foram encontradas em 64,1% dos pacientes e em 70,42% das pacientes com o quadro clássico. Quatro novas variações de seqüência foram identificadas e sua natureza sugere patogenicidade. Correlações genótipo-fenótipo foram estabelecidas.

CONCLUSÃO: Descrições clínicas detalhadas desta população brasileira de pacientes acrescenta conhecimento às correlações genótipo-fenótipo nesta grave condição, que podem auxiliar na implantação de programas de triagem de mutações.

Palavras-chave: síndrome de Rett, correlações genótipo-fenótipo.

Rett syndrome (RS) is an X-linked dominant neurodevelpmental disorder, with an estimated prevalence of one in 15000 girls¹. There is a typical evolution of the disease, although some of the girls show a variant evolution, and are described as the atypical forms of RS^1,2.

In 1999, mutations in the MECP2 gene, that encodes the methyl-CpG binding protein 2 (MECP2) were described as the cause of RS³. MECP2 binds to methylated CpG dinucleotides, through the methyl binding domain (MBD) and is involved in transcriptional silencing of genes through the transcriptional repression domain (TRD). The nature of the identified mutations indicates that they may cause total or partial loss of protein function⁴. However, results of genotype-phenotype correlations have been inconsistent across groups^5-7.

Since RS is an heterogeneous disorder, the detailed study of different patients helps understanding the clinical and evolutional variability of the disease. Mutation analysis, on the other hand, allows a better comprehension of the mutations' phenotypic effects, broadening the known clinical spectrum. This study was performed to characterize MECP2 mutations present in a large cohort of Brazilian RS patients, analyzing genotype-phenotype correlations.

METHOD

This study was approved by the Ethics Comittee of Federal University of São Paulo - Paulista School of Medicine (UNIFESP-EPM), protocol number 464/02. It was also approved by the Ethics Comittee of Biomedical Sciences Institute of São Paulo University (USP), protocol number 367. An informed consent was requested to the legal responsables of the patients, and only those with this document signed were included in the study.

All the 140 patients were examined by neuropediatricians and geneticist, following the same clinical protocol. The diagnostic criteria used to classify the patients as classical RS were those recommended by "The Rett Syndrome Diagnostic Criteria Work Group"⁸. The atypical patients fulfilled the Hagberg criteria¹, excet the minimum age of 10 years. The majority of the patients were seen at the Brasilian Association of Rett Syndrome in São Paulo, Brazil.

The data collected was used to estimate the clinical severity and to perform genotype-phenotype correlation. The severity was estimated using the scale modified by Pineda⁹.

The molecular investigation was performed at Molecular Genetics Laboratory of Genetics and Evolutive Biology Department of Bioscience Institute of USP. Genomic DNA was obtained from peripheral lymphocytes¹⁰. Point mutations in the MEP2 gene were searched by DNA amplification through polimerase chain reaction (PCR) and direct sequencing of the products. PCR and sequencing primers were designed to amplify the coding region of the gene, in 6 overlapping fragments:

Exon 2 F-5'-AAAAGGTCGTGCAGCTCAAT-3';

R-5'-GATGGCCAAACCAGGACATA-3';

Exon 3 F-5'-CTGTTTGGGGGAGGCAGAAG-3';

R-5'-CTCCATGAGGGATCCTTGTC-3';

Exon 4a F-5'- TGCCCTATCTCTGACATTGC-3';

R-5'-CACCACACTCCCCGGCTTTC-3';

Exon 4b F-5'-GAAGCGAAAAGCTGAGGCCG-3';

R-5'-GGAGCTCTCGGGCTCAGGTG-3';

Exon 4e F-5'-CCCCCAAGAAGGAGCACCA-3';

R-5'-ACAATGTCTTTGCGCTCTCC-3';

Exon 4f F-5'-CCCAAGGAGCCAGCTAAGAC-3';

R-5'-CAGAGCCCTACCCATAAGGAG-3'.

Each fragment had specific cycling parameters and all had an inicial denaturing of 94ºC for 5 minutes and final extension of 72ºC for 10 minutes. Exon 2 and 4a used 30 cycles of 94ºC for 45 seconds, 58ºC for 45 seconds and 72º C for minute. Exon 4b used 30 cycles of 94ºC for 45 seconds, 60º C for 45 seconds and 72º C for minute. Exons 3, 4e and 4f used 14 cycles of 94ºC for 30 seconds, 69º C for 40 seconds lowering 0.5ºC per cycle and 72ºC for a minute and half, followed by 24 cycles of 94ºC for 30 seconds, 62º C for 40 seconds and 72º C for a minute and half. Amplification quality was verified in agarosis gel. PCR products were purified and quantified before been submitted to a sequencing reaction, on both strands. Reactions were analyzed in automatic sequencer ABI Prism model 310, version 3.0, using big dye (Amersham-Pharmacia^®), according to the manufacturer's instructions. Sequences were compared to normal MECP2 sequence (Genbank L37298/AF030876). Thirty-five patients were excluded because of structural alterations found in the MECP2 gene (detected or suspected).

Based on clinical evaluation and point mutations found, a genotype-phenotype correlation was performed, with respect to presence or absence of mutation, type and location of mutations and between the three most frequent mutations.

Statistical analysis of the results was performed using: (1) Chi-square test¹¹, to study associations between groups and studied variables; (2) Mann-Whitney test¹¹ to confront diferent mutation types and the presence or not of a mutation in relation to scores on the Pineda scale⁹; (3) Kruskal-Wallis variance analysis¹¹ to study scores on the Pineda scale⁹ and the location of the mutation and between the three most frequent mutations. The level of rejection of null hypothesis was fixed in 0.05 or 5%.

RESULTS

Patients

One hundred and forty female patients were evaluated with clinical hypothesis of RS. Thirty-five patients were late excluded because of large structural alterations found in the MECP2 gene (detected or suspected). Beetween the remaining patients, there were 2 pairs of concordant twins. Among the 105 patients, 68% had classical RS and 27% were atypical. Five patients were not classified due to their age, or because they showed an initial very suggestive clinical picture, but the diagnostic criteria were impossible to apply; they were categorized as "non-classified". The median age of the patients on the first evaluation was 8 years (SD 5.44 years), ranging from 1 year and 7 months and 27 years and 11 months of age.

Mutations

In total, 84 point variations were found in 74 patients, including the 2 pairs of twins, resulting in a frequency of detection fo 70% (72/103, considering twins as one) (Fig 1). Of them, 68 were considered pathogenic (81% of all variations), and 4 were not previously described. Twelve were silent variations (14.3% of all variations); 1 not previously described. Three missense non-pathogenic polymorfisms (3.65% of all variations), previously described, and an alteration whose pathogenicity was not been previously determined were also found (1.1% of all variations). Six patients had only non-pathogenic variations (5.8%). C to T transitions at CpG islands totalizes 88.1% (74/84). Most of the pathogenic point mutations were concentrated on the methyl binding domain (MBD) (25/66 - 36%). The frequency of pathogenic point mutations was 64.1% (66/103). The distribution of pathogenic point mutations is shown in Figure 2.

Three patients deserve special consideration. Two were atypical, one had hyperchromic linear spots and normal karyotype and the other had a chromosomal abnormality, t(4)(q11);14(q11). None of them had any detected point mutation. The third patient had a classical phenotype but high levels of lactic and pyruvic acids. This patient had the T158M mutation, previously described. All were included because it was considered interesting to check if they had MECP2 mutations.

Among the classical patients, the frequency of detection of pathogenic point mutations was 70.4% (50/71, twins considered as 1). Among the atypical patients, the frequency was 50% (14/28), and among the non-classified patients, 40% (02/05). The four most frequent mutations amounted to 68% of the pathogenic point mutations detected in the classical patients and 50% in the atypical ones.

The distribution of pathogenic point mutations detected among the atypical patients was 58.8% (10/17) in those with forme fruste; 33.3% (2/6) in those with congenital variation; 66.7% (2/3) in those with late regression and none in those with early seizure.

Genotype-phenotype correlation

Presence or absence of a pathogenic mutation - Initially, the patients were grouped according to the presence or absence of a detected pathogenic point mutations (Table 1). Patients with pathogenic point mutations are more likely to exhibit the classical form (p=0.056) and breathing irregularities (p=0.006). Patients without detected pathogenic point mutations presented earlier onset of disease (p=0.013).

Type of mutation - The mutations were divided into two different groups: (1) missense mutations and (2) truncating or nonsense mutations (Table 2). Patients with truncating mutations had earlier symptoms, before one year of age (p=0.005), as they had higher scores with Pineda scale⁹ (p=0.032) (Table 5).

Location of the mutation - The location of the pathogenic point mutations in the MECP2 protein was divided into four groups: (1) mutations in the MBD; (2) mutations between the MBD and the TRD; (3) mutations in the nuclear location signal (NLS) and (4) mutations in the transcriptional repression domain (TRD) after the NLS (Table 3). Mutations at the terminal carboxi region were not correlated. Patients with mutations at NLS had symptoms before one year and this almost reached statistical significance (p=0.066). Patients with mutations in the TRD after NLS were more likely to maintain ability to walk (p=0.010). Patients with mutations in NLS and between domains had higher scores with Pineda scale⁹ in comparison to patients with mutations in TRD after NLS, that had lower scores (p=0.027) (Table 5).

Three most frequent mutations - The three most frequent pathogenic point mutations, T158M, R306C, R168X, were used to perform a more specific genotype-phenotype correlation (Table 4). All of them were more frequent among patients with classical form. Patients with the R306C mutation had late symptoms (p=0.007) and were more likely to maintain the ability to walk (p=0.029). They also reached lower scores with Pineda scale⁹ (p=0.021) (Table 5).

DISCUSSION

Patients

It is known that RS is more frequent and shows a higher phenotypic variation than was first realized¹. Published Brazilian studies grouped few patients^12-14 and none performed a molecular caracterization. This is the first study in a large group of Brazilian RS patients with molecular characterization and genotype-phenotype correlation.

The majority (68%) of the studied patients had the classical form of the disease. Since the evaluation of a patient at an initial stage is more difficult, five of the patients were grouped as non-classified. In three of them, there were no pathogenic point mutations detected, although they have a very suggestive clinical picture. All of these three patients have less than 2 years, and the clinical follow-up will be mandatory for the establishment of a diagnosis.

Mutations

MECP2 mutations have been identified in 70-90% of sporadic patients and approximately 50% of familial cases¹⁵. In this study, pathogenic mutations were found in 64.1% of all patients, 70.4% of classical RS patients, 50% of atypical patients and 40% of non-classified patients (Fig 2). Four pathogenic point mutations were more frequent - T158M, R306C, R168X and R270X, amount to 68% of pathogenic point mutations in classical patients and 50% of atypical patients, indicating that these mutations should be initially searched in screening programs with Brazilian RS patients.

Four not previously described point mutations were found. The first one, K112X, was not described on RettBASE¹⁶, a database that collects MECP2 mutations. It was found in association with another described alteration, S291A, whose pathogenicity was questioned. The aminoacid K in that position of the MECP2 gene is conserved in all species and the mutation leads to an early stop codon, and therefore a truncated protein. This suggests that K112X is pathogenic and S291A is not.

The other three new mutations were S134P, F157L and X487L. At codon 134, there have been 2 different mutations described: S134C, pathogenic, and S134F, whose pathogenicity is unknown¹⁶. This is a conserved residue in MBD in all species, polar, whith a hydrophilic behaviour, and it was substitute by a non-polar hydrophobic aminoacid, which suggest that S134P should be pathogenic. At codon 157, there have also been 2 different mutations described: F157fs, pathogenic and F157I, whose pathogenicity is unknown. This is also a conserved aminoacid in all species, which suggest pathogenicity. The mutation X487L abolishes the final codon, which prevents the stop of the transcription, leading to a large protein, suggesting pathogenicity.

The classical patient with higher lactic and pyruvic acids had the T158M mutation. The elevation of blood levels of lactic acid and/or pyruvic acid is found in a substantial proportion of patients with RS and can be associated with ventilation disturbances¹⁷. The identification of a pathogenic mutation in this patient reinforces the findings of Huppke et al.¹⁸ , who emphasized that the diagnosis of RS should not be dismissed because some characteristic features are absent or because uncharacterisic symptoms are present.

In this study, only the coding region of MECP2 has been analyzed, and mutations in regulatory elements could account for those cases in which no mutation has been identified¹⁵. In addition, PCR-based techniques could miss the altered gene if there is large rearrangements. Without amplification of the mutated allele, only the normal allele is amplified, resulting in false-negative results, and accounting for detection rates lower than a 100%¹⁹.

A recently published recommended screening strategy is to firstly screen exons 3 and 4 for mutations using PCR-based techniques²⁰. If no mutation is identified, further screening of exons 1 and 2 is reccomended. For individuals in whom no pathogenic mutations have been found, additional screening for large deletions is recommended, which may be achieved by Southern analysis, quantitative PCR or multiplex ligation prove amplification (MLPA). Patients who are negative for MECP2 mutations and have a strong clinical diagnosis of RS, particularly if there are early onset seizures, should be considered for further screening of the CDKL5 gene, recently associated with this variant²⁰.

Genotype-phenotype correlations

The discovery of a molecular alteration related to RS raised questions about a possible genotype-phenotype correlation; however various studies in different populations have yielded inconsistent results^6,7,21-24.

There are different genetic factors that are likely to influence the phenotype in RS, including patterns of X chromosome inactivation and the type and location of the mutation. Several studies have demonstrated normal X inactivation patterns in the majority of RS cases, so this should be an important factor in a minority of patients^5,24.

Presence or absence of a pathogenic mutation - Before correlating the different types or locations of the mutations and the phenotype, a correlation between the presence or absence of a pathogenic mutation and the clinical picture was done (Table 1). It was observed that most patients with an unidentified pathogenic point mutation (74.3%) had an earlier onset of symptoms, before one year of age. A similar observation was made in 20 Korean RS patients, where there was a tendency for patients with no detected MECP2 mutation (30%) to show more severe symptoms and more rapid clinical progression²³. We suggest that these patients have large structural abnormalities in the MECP2 gene, not detectable by our screening strategy, causing total loss of protein function and therefore the earlier disease presentation. Additional molecular methodologies are necessary to confirm this hypothesis.

In this study, breathing abnormalities were significantly more frequent in patients with identified point mutations. Breathing abnormalities are a striking feature of RS that occurs during wakefulness⁵, and its association with a point mutation reinforces the specificity of the mutations in respect of the classical phenotype. Additional associations observed in patients with detected mutations were pointed by Bienvenu et al.²⁵, that showed that patients with detected mutation lost more frequently acquired purposefull hand skills, had more frequent peripehral vasomotor disturbances and epilepsy and were more frequently able to walk, although statistically not significant.

Type of mutation - Several groups tried to determine whether different types of mutations in the MECP2 gene can account for the variability of clinical features. We divided the mutations found in this study in two different groups: missense and truncating mutations (Table 2). In agreement with other studies^6,24,26,27, we found that patients with truncating mutations had earlier symptoms and higher scores with Pineda scale⁹ (Table 5), indicating that these mutations are more deleterious to the protein.

Location of the mutation - The mutations were also grouped according to their location in the different regions of the MECP2 gene (Table 3), and it is expected that mutations in more important functional protein regions lead to more severe phenotypes. Indeed, we found that mutations in the NLS lead to earlier disease onset and higher scores with Pineda scale⁹. In contrast, patients with mutations in the TRD domain after the NLS had lower scores, presenting the atypical form of the disease.

These results are similar to those of Colvin et al.²⁸, and they indicate that mutations involving the NLS may result in failure of the protein to be directed to the nucleus, resulting in a more significant reduction of MECP2 protein function, which in turn would lead to a more severe phenotype. Proteins carrying mutations distal to the NLS might still be targeted to the nucleus and exert a partial effect on transcription repression²⁸.

Three most frequent mutations - Finally, the three most common mutations were considered individually (Table 4), searching to a more precise genotype-phenotype correlation. It might happen that a specific mutation could be responsible for a specific symptom or cause a more severe phenotype.

All of the three mutations were more frequent in classic RS. In accordance with other studies^27,29, we observed that the R306C mutation was associated with a milder form of RS that included later disease onset, lower scores with Pineda scale⁹, and more frequently retention of the ability to walk. A functional assay showed that R306C mutation retained the ability to repress transcription, accounting for the milder phenotypes³⁰.

We found that presence, type and location of mutations do not influence all features of RS in the same way, as observed by other studies^5-7,18,20-29. It is necessary more studies on protein function and genotype-phenotype correlations with higher number of patients to better interpret these findings.

In conclusion, this is the first study with molecular characterization of a large sample of Brazilian RS patients. A genotype-phenotype correlation was shown, providing valuable information necessary for genetic and clinical counseling. Although still tentative, genotype-phenotype correlations helps answering questions raised by parents and caretakers about the meaning of a particular molecular alteration found. When a negative test result is obtained, it should be emphasized that additional molecular alterations could be present, not detected by the methodology used, or different altered genes could be involved and, because of that, the clinical interpretation of this result should be made with caution. The results also show that mutation screening in Brazilian RS patients should begin by searching for the four most frequent mutations identified here. It is also suggested that methods that detect large deletions should be used, mostly when analyzing early onset and atypical patients.

Received 16 February 2009, received in final form 6 May 2009.

Accepted 16 June 2009.

Dra. Fernanda Teresa de Lima - Rua Botucatu 740 / Disciplina de Genética / UNIFESP-EPM - 04023-062 São Paulo SP - Brasil. E-mail: [e-mail]

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Publication Dates

• Publication in this collection
  21 Aug 2009
• Date of issue
  Sept 2009

History

• Accepted
  16 June 2009
• Reviewed
  06 May 2009
• Received
  16 Feb 2009