- Research article
- Open Access
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DNA instability in replicating Huntington's disease lymphoblasts
© Cannella et al; licensee BioMed Central Ltd. 2009
- Received: 24 June 2008
- Accepted: 11 February 2009
- Published: 11 February 2009
The expanded CAG repeat in the Huntington's disease (HD) gene may display tissue-specific variability (e.g. triplet mosaicism) in repeat length, the longest mutations involving mitotic (germ and glial cells) and postmitotic (neurons) cells. What contributes to the triplet mutability underlying the development of HD nevertheless remains unknown. We investigated whether, besides the increased DNA instability documented in postmitotic neurons, possible environmental and genetic mechanisms, related to cell replication, may concur to determine CAG repeat mutability. To test this hypothesis we used, as a model, cultured HD patients' lymphoblasts with various CAG repeat lengths.
Although most lymphoblastoid cell lines (88%) showed little or no repeat instability even after six or more months culture, in lymphoblasts with large expansion repeats beyond 60 CAG repeats the mutation size and triplet mosaicism always increased during replication, implying that the repeat mutability for highly expanded mutations may quantitatively depend on the triplet expansion size. None of the investigated genetic factors, potentially acting in cis to the mutation, significantly influence the repeat changes. Finally, in our experiments certain drugs controlled triplet expansion in two prone-to-expand HD cell lines carrying large CAG mutations.
Our data support quantitative evidence that the inherited CAG length of expanded alleles has a major influence on somatic repeat variation. The longest triplet expansions show wide somatic variations and may offer a mechanistic model to study triplet drug-controlled instability and genetic factors influencing it.
- Lymphoblastoid Cell Line
- Triplet Expansion
- Nondividing Neuron
- Triplet Change
The Huntington's disease (HD) mutation influences age at onset through its CAG repeat length, a genetic feature that is unstable during intergenerational parent-child transmission . Transmitting males generally cause the highest expansions in successive generations. Expansion size progressively increases through a so-called multi-step mechanism [2, 3], thus providing the molecular explanation for onset anticipation. Large CAG expansions above 60 repeats cause a severe phenotype leading to juvenile HD (JHD) . The higher the expanded repeat length, the more instable is the triplet stretch in somatic and germline tissues [5–10]. In the brain of patients with another CAG expansion mutation disease, dentato-rubral pallido-luysian atrophy (DRPLA), dividing glial cells carry the largest CAG mutations [11, 12], whereas, in HD, differentiating nonreplicating neurons carry the largest expansion mutations [13, 14]. In other non-CAG triplet diseases with an excess of repeat expansions involving thousands of trinucleotides, somatic time-dependent variation in a CTG or GAA polymorphic stretch in the mutated alleles has also been documented in lymphoblasts, indicating lymphoblastoid cells as a valuable source for longitudinal analyses of triplet instability, mosaicism variability and genetic transmission [15, 16].
Our purpose in this study was to investigate whether, besides the mechanisms influencing the CAG repeat mutability in HD terminally differentiated and nondividing neurons [13, 14], cell division may contribute to DNA instability. To do so, we sought possible length- and time-dependent variability in the HD gene in serially passaged lymphoblastoid cell lines established from patients, after their passages in culture over time. We also studied the possible dependence of the somatic triplet variation and mosaicism (heterogeneity of the repeat length in the tissue) on CAG mutation length, on factors acting in cis or in trans to the mutation, and on drug-induced contraction of the mutation size.
Passaged cell lines and DNA study
Demographic characteristics of the patients and genetic characteristics of the lymphoblastoid cell lines in the patients with Huntington's disease.
expanded CAG ± SD
Age at onset ± SD
Mosaicism degree ± SD
(triplet changes in %)
Lymphoblats with low mutation penetrance
40.167 ± 0.983
57.250 ± 5.62
0.167 ± O.408
6.333 ± 1.966a
(1/6 or 17%)
Lymphoblats with usually expanded mutation penetrance
45.628 ± 3.471
40.643 ± 10.094
0.628 ± 0.874
7.442 ± 2.797b
(17/43 or 39%)
Lymphoblasts with high mutation penetrance
80 ± 21.042
12.750 ± 8.396
3.429 ± 1.512
(2 ≥ 5)
15.429 ± 11.238c
(9/9 or 100%)d
50.397 ± 15.416
37.741 ± 14.819
0.929 ± 1.333
8.321 ± 5.250
(27/58 or 46%)
For allele length analyses, genomic DNA was purified from blood lymphocytes, and lymphoblastoid cell lines containing about 1–3 × 106 cells, using standard procedures (see Additional file 1 and ). To elucidate potential factors acting either in cis or in trans with HD mutations, we also analysed CCG repeat size, deletion of the glutamic acid residue (ΔG) at nucleotide position 2642 of the HD gene, and the CAAΔCAG mutation in the 12 base pair region between CAG and CCG repeats, on both normal and mutated genes using previously described techniques . All data concerning subjects' demographic features, cell-line mutation length and repeat number variation are included in Table 1.
Analysis of somatic CAG repeat changes and mosaicism degree in passaged lymphoblasts
Cell-line drug treatment
In an attempt to reduce the mutation size and stability, we tested drugs influencing some of the suggested mechanisms potentially related to triplet instability . For drug treatment experiments, two "stable" and two particularly "unstable" and prone-to-expand cell lines (of 74 and 85 CAG repeats) were selected. We treated cell lines with the following drugs: ethylmethanesulphonate (EMS), a GC/AT modifier thought to prevent CAG expansion in lymphoblasts derived from patients with myotonic dystrophy type 1 ; ethidium bromide (EB), a DNA intercalating drug reducing the rate of repeat expansion by inhibiting enzymes that bind to DNA ; and mitomycin C (Mit-C), an interstrand crosslinker . Each progenitor culture was split into multiple aliquots: four flasks for drug treatment (one each for EMS, EB and Mit-C) and one flask for control. Each treatment was performed in duplicate. All cultures were serially passaged as previously described and maintained in parallel throughout the experiments (for further cell line culture and drug treatment methodology see Additional file 1).
For statistical analysis we used nonparametric tests: Mann-Whitney U test, to compare differences between cell lines with different ΔCAG (small triplet changes with ΔCAG ≤ 3 vs large triplet changes ≥ 5), and Kruskal-Wallis test to compare differences across more than two groups. A simple regression model was used to test the linear dependence of the maximum number of peaks (CAG mutation mosaicism) on expanded CAG repeats. Data are presented as means ± SE. Statistical analysis was performed with Stat View V (tests considered significant at p ≤ 0.05).
Expanded CAG repeat size-dependent changes
Triplet variation varied over culture time in a CAG length-dependent manner (Table 1). Most passaged cell lines showed no or minimal (1 to 3 repeats) over-time triplet variation (51/58 cell lines or 88%; Table 1), including small contraction or expansion events. The repeat changes obtained in each cell line ranged between 0 in magnitude (ΔCAG = 0, n = 31) and > 1 [ΔCAG > 1, n = 27; Group 1 (n = 11), 2 (n = 8), 3 (n = 3), or ≥ 5 (n = 5)], according to the number of expanded or contracted repeats or both, during 6-month culture (see Additional files 1, 2, 3 and Table 1). Cultured cell lines showing over-time triplet variation (and ΔCAG greater than 5) had, on average, a larger CAG repeat number than cell lines with no or little somatic variation (p < 0.0001, Figure 1A). The magnitude of ΔCAG significantly correlated with the size of the expanded CAG repeat: the more expanded the repeat number was, the higher were the ΔCAG values (p values ranged from 0.0041 to < 0.0001, Figure 1B). All cell lines, regardless of their ΔCAG values, exhibited some degree of triplet mosaicism (i.e., repeats varied in size). The degree of mosaicism invariably increased significantly in cell lines carrying large expansions and ΔCAG ≥ 5 (p < 0.0001, Figure 1C). The maximum number of peaks (e.g. the level of triplet mosaicism indicating a mutation rate degree in a certain tissue) significantly correlated with ΔCAG magnitude (Figure 1D).
No significant association of investigated in cis and in trans factors influenced the repeat variation in our cohort of cell lines (see Additional file 1). Nor did we ever observe the CAAΔCAG mutation in the 12 base-pair region between CAG and CCG repeats, on either normal or mutated genes, regardless of ΔCAG values.
Drug-induced CAG contraction
The relatively small magnitude of triplet changes and length gains we observed in most cell lines (88% of total) confirms that cell-division related events contribute minimally to HD instability and is in agreement with the recent findings concerning CAG repeat changes mainly occurring in terminally differentiating nondividing neurons [13, 14, 26]. The only exception in our model were the very large expansion mutations showing increased over-time gains of CAG variations in dividing cells (see Additional file 2, Figures 1 and 2, Table 1). Lymphoblasts with highly expanded mutations are particularly prone to oxidative stress [27, 28] and decreased mitochondrial ATP production . More recent research has proposed a model taking into account a relationship between oxidative lesions accumulating in brain and progressive somatic gains in expanded repeats resulting from errors in repairing . Hence besides mechanisms determining DNA instability as reported in differentiating neurones [13, 14, 26], CAG mutability might have arisen also from an age related oxidative-stress in highly expanded lymphoblasts ample evidence shows that JHD patients show extended brain damage associated with a particularly severe phenotype  and large mutations cause JHD, we conjecture that the cell division occurring in glial cells with large mutations may contribute to an excess of expanded repeat gains, thus contributing to more widespread brain disease, as happens in DRPLA [11, 12]. This observation is in line with the hypothesis that in certain cases of HD, mutation length gains may continue to accumulate during life, as the disease progresses .
Consistent with a previous report , we found no influence on instability of the analysed factors potentially acting in-cis to the mutation (see Additional file 1), including the CAAΔCAG mutation in the 12 bp region between the CAG and CCG repeats, described by Goldberg et al. . This apparent discrepancy may depend on the fact that Goldberg et al. studied a population of variable ethnic origin whereas ours was an ethnically homogeneous population . Because all our cell lines showed the CAA codon on both alleles in the 12 bp region between the CAG and CCG repeats, regardless of the CAG repeat variation, we therefore rule out even the potential effect of such a factor potentially acting in trans with the CAG repeat instability in our population. The role of the normal allele size to test the hypothesis of whether the CAG repeat polymorphism in the non-HD range is a potential physiological modifier of mutation instability [29, 31–33] remains to be investigated.
To reduce in vitro the mutation length of particularly large and unstable expansions and to approach a potential therapeutic strategy, we treated two cell lines with drugs thought capable of influencing mechanisms of instability [21, 22, 25]. When we used drugs interfering with diverse mechanisms to treat two cell lines carrying large mutations and particularly prone-to-expand, the expanded (but not the normal allele) repeat number contracted, and the bi-modal intra-allele CAG distribution progressively disappeared (Figure 2). Hence, we presume that many different mechanisms act in concert to influence CAG repeat instability. Given that somatic repeat expansion affects the HD phenotype, this finding provides useful information insofar as contracting the longest repeat number is among the putative pharmacological strategies for use in patients with HD, particularly when high expansion mutations cause early age at onset [22, 25]. Intriguing questions left open for future research include the mechanisms underlying triplet repeat expansion (e. g. replication, recombination and repair processes), and their drug-induced contraction.
The main limitation of our model is probably cell proliferation induced by an infecting virus. Indeed, as recently demonstrated in HD patients, mutation length gains of CAG repeats may even occur in somatic cells or neurons well after these cells are terminally differentiated and mitotic replication has ceased. The fact that our proliferating cell model mostly disclosed small contraction/expansion changes in few triplets nevertheless theoretically offers further strength and support to evidence that repeat length gains may occur independently of replication, as demonstrated in the striatal neuronal population [13, 14, 26]. An additional limitation of our work may depend on the limited (two) repetitions of the experiments. This was due to the relatively large number of cell lines cultured for long times (at least six months) with a relevant number of PCR assays required and performed each week (see Methods and Additional file 1). Therefore, the inter-experimental reproducibility is unknown as statistical significance could not be determined from the limited (two) repetitions of the experiments. Despite the potential limitations of this and other studies [15, 16, 27–29, 34], i.e. the biological influence of the infecting virus on immortalised cells and the inter-experimental reproducibility, our study may offer an in vitro approach to human cells in the attempt to provide a new experimental model system for mechanistic studies of triplet expansion (mitotic vs repair synthesis or other mechanisms so far reported) and clinical treatments for HD.
Our study offers further relevance to the hypothesis that the repeat mutability depends quantitatively on CAG triplet expansion size. The longest triplet expansions show wide somatic variations and may offer a mechanistic model to study triplet drug-controlled instability. Replication does not affect somatic variability in most of the cell lines whose CAG expansion size ranges in the usual mutation penetrance confirming that cell-division related events contribute minimally to HD instability, in agreement with the findings concerning CAG repeat changes mainly occurring in terminally differentiating nondividing neurons. Instead, large repeat expansions causing JHD tend to expand during replication supporting the hypothesis that mechanisms affecting CAG mosaicism and mutability may differ in dependence on the mutation length, in certain tissues, and as the disease progresses. In our experiments certain drugs controlled triplet expansion in prone-to-expand HD cell lines carrying large CAG mutations. Finally, we found no influence on instability of the analysed factors potentially acting either in cis or in trans with the mutation, including the CAAΔCAG mutation in the 12 bp region between the CAG and CCG repeats.
We thank the European Huntington's Disease Network, all patients and their families (Associazione Italiana Corea di Huntington-Neuromed), the Italian Health Ministry and Siena Biotech (FS, COFIN 2006), for their kind cooperation and support. The financial support of Telethon – Italy to FS (Grant no. GGP06181), is gratefully acknowledged.
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