Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan
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- Sakai, H., Yoshida, K., Shimizu, Y. et al. Neurogenetics (2010) 11: 409. doi:10.1007/s10048-010-0245-6
Spinocerebellar ataxia type 31 (SCA31) is a recently defined subtype of autosomal dominant cerebellar ataxia (ADCA) characterized by adult-onset, pure cerebellar ataxia. The C/T substitution in the 5′-untranslated region of the puratrophin-1 gene (PLEKHG4) or a disease-specific haplotype within the 900-kb SCA31 critical region just upstream of PLEKHG4 has been used for the diagnosis of SCA31. Very recently, a disease-specific insertion containing penta-nucleotide (TGGAA)n repeats has been found in this critical region in SCA31 patients. SCA31 was highly prevalent in Nagano, Japan, where SCA31 accounts for approximately 42% of ADCA families. We screened the insertion in 94 SCA31 patients from 71 families in Nagano. All patients had a 2.6- to 3.7-kb insertion. The size of the insertion was inversely correlated with the age at onset but not associated with the progression rate after onset. (TAGAA)n repeats at the 5′-end of the insertion were variable in number, ranging from 0 (without TAGAA sequence) to 4. The number of (TAGAA)n repeats was inversely correlated to the total size of the insertion. The number of (TAGAA)n repeats was comparatively uniform within patients from the three endemic foci in Nagano. Only one patient, heterozygous for the C/T substitution in PLEKHG4, had the insertions in both alleles; they were approximately 3.0 and 4.3 kb in size. Sequencing and Southern hybridization using biotin-labeled (TGGAA)5 probe strongly indicated that the 3.0-kb insertion, but not the 4.3-kb insertion, contained (TGGAA)n stretch. We also found that 3 of 405 control individuals (0.7%) had the insertions from 1.0 to 3.5 kb in length. They were negative for the C/T substitution in PLEKHG4, and neither of the insertions contained (TGGAA)n stretch at their 5′-end by sequencing. The insertions in normal controls were clearly detected by Southern hybridization using (TAAAA)5 probe, while they were not labeled with (TGGAA)5 or (TAGAA)5 probe. These data indicate that control alleles very rarely have a nonpathogenic large insertion in the SCA31 critical region and that not only the presence of the insertion but also its size is not sufficient evidence for a disease-causing allele. We approve of the view that (TGGAA)n repeats in the insertion are indeed related to the pathogenesis of SCA31, but it remains undetermined whether a large insertion lacking (TGGAA)n is nonpathogenic.
Spinocerebellar ataxia type 31 (SCA31), formerly known as 16q22.1-linked autosomal dominant cerebellar ataxia (16q-ADCA), is a recently established subtype of ADCA characterized by adult-onset, pure cerebellar ataxia [1–6]. SCA31 accounts for 8–17% of ADCA families and is the third most predominant ADCA subtype after SCA6 and MJD/SCA3 in Japan [7–11]. A single nucleotide substitution (–16C>T) in the 5′-untranslated region (UTR) of the gene encoding puratrophin-1 (PLEKHG4) has been shown to be a disease-specific marker for 16q-ADCA [4, 5]. However, this specific substitution has been found exclusively in the Japanese population ; thus, it is still unclear whether SCA31 exists in countries other than Japan.
Two patients with SCA31 have been found not to carry this substitution in PLEKHG4 [5, 13], indicating that it is not a disease-causing mutation for SCA31. Thereafter, Amino et al.  narrowed the SCA31 critical region to 900 kb between rs11640843 (SNP04) and PLEKHG4 by fine single nucleotide polymorphism (SNP) typing. Sato et al.  identified an inserted sequence in this region, which was confirmed in all SCA31 patients, without exception. The insertion consists of complex penta-nucleotide repeats containing (TGGAA)n, and the size of the insertion is variable, ranging from 2.5 to 3.8 kb in length, among patients .
We have shown that SCA31 is the most predominant subtype of ADCA in Nagano, which is located in the central, mountainous district of the main island of Japan [13–15], see Fig. 2]. To date, we have analyzed 168 ADCA families from Nagano and diagnosed 71 families (42%) with SCA31. Thus, the frequency of SCA31 in Nagano is much higher than in other areas of Japan [7–11]. We have found that SCA31 families are highly prevalent in particular areas of Nagano, named as Kiso, Ina, and Saku [13–15], see Fig. 2]. The ratio of SCA31 families to total ADCA families in these areas was 14/16 (88%, Kiso area), 12/18 (67%, Ina area), and 17/25 (68%, Saku area).
Here, we have screened an insertion mutation for SCA31 in 94 patients from 71 families in Nagano.
Materials and methods
Subjects and clinical evaluation
We recruited 94 patients from 71 families with SCA31, and these families most probably originated from Nagano. The diagnosis of SCA31 was based on the presence of the C/T substitution in PLEKHG4 (92 patients from 70 families). Two patients (from two families) without the C/T substitution in PLEKHG4 were also included in this study because they had a disease-specific haplotype in the 900-kb SCA31 critical region . Forty-four of 71 families (62%) originated from the three endemic foci described above. Detailed medical interviews and routine neurological examinations were performed by expert neurologists. Age at onset was determined on the basis of the information provided by the patients or their close relatives. Scales for the assessment and rating of ataxia (SARA) were used for the assessment of cerebellar ataxia. To minimize the interrater variability, SARA was performed by either of two expert neurologists (KY and YS) for 57 patients (67 times).
This research protocol was approved independently by the Ethical Committee of Shinshu University School of Medicine and by the Committee for Ethical Issues at Yokohama City University Graduate School of Medicine.
The insertion sequence was amplified by PCR according to the methods described by Sato et al. . PCR products were purified using a PCR purification kit (QIAGEN), digested with HaeIII, and then separated on a 0.8% agarose gel (25 V, 15 h). The size of the HaeIII fragment containing the insertion was calculated with a DNA size marker simultaneously electrophoresed as a reference. HaeIII-undigested PCR products were separated in a 0.8% low-melting agarose gel, and fragments of approximately 3.0 kb were cut out and extracted using a QIA quick® Gel Extraction Kit (QIAGEN). They were then directly sequenced by a standard protocol using BigDye terminator (Applied Biosystems, Foster City, CA) on an ABI PRISM 3100 Genetic analyzer or an ABI PRISM 3500xL Genetic analyzer (Applied Biosystems). HaeIII-undigested PCR products were also separated in a 1% agarose gel, blotted to a nylon membrane (HybondTM- N+, Amersham International plc, Buckinghamshire, UK) using 10× SSC, and subjected to Southern hybridization using biotin-labeled (TGGAA)5, (TAGAA)5, or (TAAAA)5 as a probe. Detection was done with BrightStarTM BioDetectTM Nonisotopic Detection Kit (Ambion Inc., Austin, TX) according to the manufacturer’s instructions.
The relationship between the size of the insert and the age at onset was analyzed using Spearman’s correlation coefficient by rank test. Regression analysis for SARA data was also performed. Analysis of the differences in the insert size among the groups was carried out using analysis of variance and the post hoc test of Scheffé. The level of significance was set at p < 0.01.
The haplotypes of SCA31 patients and control subjects
Polymorphic marker (site on NCBI Build 36.3)
Complex penta-nucleotide repeat insertion [insertion size] (65,081,803)
–16C/T puratrophin-1 (65,871,433)
Frequencies in controlsa
5′ TCAC (TGGAA)n (TAAAA TAGAA)n--
Patient (ID 254)b
5′ TCAC TAAAA (TAGAA)4 (TGGAA)n -- [3,040 bp]
5′ TCAC TAACA (TAAAA)n -- [4,280 bp]
5′ TCAC TAACA (TAAAA)n -- [3,520 bp]
5′ (TAAAA)n -- [2,540 bp]
5′ (TAAAA)n -- [1,070 bp]
In the present study, we confirmed that all of the SCA31 patients in our cohort had the insertions of the penta-nucleotide repeats found by Sato et al. . The insertions ranged from 2.6 to 3.7 kb in length, and contained (TGGAA)n stretch at their 5′-end, without exception. We also verified that the size of the insertion was inversely correlated to the age at disease onset in our large cohort. However, the size of the insertion seemed not to be associated with the disease progression rate after onset.
We found that the penta-nucleotide (TAGAA)n repeats at the 5′-end of the insertion were variable in number, as were the subsequent (TGGAA)n repeats. Interestingly, the number of (TAGAA)n repeats, if present, was inversely correlated with the total size of the insertion. Furthermore, the repeat size of (TAGAA)n is comparatively uniform within the endemic foci. From the geographical viewpoint, we previously supposed that there were two major foci in the southwest (Ina–Kiso) and east (Saku) areas in Nagano , but patients in Ina and Kiso areas are likely to be different from the viewpoint of population genetics because the number of (TAGAA)n repeats and the size of the insertion were obviously different between the two groups.
In our cohort, only one patient (patient ID 254) was homozygous for the insertion in the SCA31 critical region as determined by PCR analysis (Fig. 5, Table 1). Contrary to our expectation, sequencing showed that only the smaller 3.0-kb insertion had (TGGAA)n stretch. This was also confirmed by Southern hybridization using biotin-labeled (TGGAA)5 probe. The patient developed gait ataxia at approximately age 76 and showed pure cerebellar ataxia by neurological examination at age 87. His clinical features were typical for SCA31 [7–11, 13, 15]. As his parents died a long time ago, we could not obtain reliable information on his parents or their genomic DNA. It is confusing that he was heterozygous for the C/T substitution in PLEKHG4 but was homozygous for a disease-specific G/A substitution at AB473220 (Table 1).
Moreover, three control individuals had the insertions ranging from 1.0 to 3.5 kb in length. Sequencing and Southern hybridization indicated that these insertions did not contain (TGGAA)n or (TAGAA)n repeats. Information on the family history of cerebellar ataxia was not available for these control individuals because they voluntarily participated in this study as anonymous healthy controls. Neither of them carried the C/T substitution in PLEKHG4, but one control individual (control 1 in Table 1) had G/A substitution at AB473220 and a large insertion (3,520 bp) indistinguishable from SCA31 patients. Sato et al.  have shown that the insertion in the SCA31 critical region is rarely observed in control individuals but that the insertion in control individuals is shorter in length than SCA31 patients and lacks (TGGAA)n stretch. At present, however, we do not completely exclude the possibility that the 4.3-kb insertion in patient ID 254 and the 3.5-kb insertion in control 1 have some pathogenic effects, although these insertions are likely to lack (TGGAA)n stretch.
In summary, our data clearly indicate that not only the presence of the insertion but also the size of the insertion in the SCA31 critical region is insufficient evidence for the disease-causing allele. They may support the hypothesis by Sato et al. that the presence of (TGGAA)n repeats is important for the pathogenesis of SCA31. However, it is possible that a large insertion without (TGGAA)n repeats may have a pathological significance, requiring further investigation. The control individual with such insertion in this study may potentially develop cerebellar ataxia in the future, considering that SCA31 is a late-onset disease. The insertion sequences in SCA31 patients consist of (TAGAA), (TGGAA), and (TAAAA) penta-nucleotide repeats of variable numbers , but the precise pathogenesis by the penta-nucleotide repeat insertion remains unclear in SCA31. Further detailed characterization of the inserted sequence and data on genotype–phenotype correlation will be needed.
We are grateful to the clinicians who provided us with information on their patients, and the patients and their families who participated in this study. This work was supported in part by a Grant-in-Aid for Science Research from the Ministry of Education, Science and Culture, Japan (KY and NM); a grant from the Research Committee for Ataxic Diseases, the Ministry of Health, Labour, and Welfare, Japan (KY); and a grant from the Ministry of Health, Labour, and Welfare, Japan (NM).
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