Cyclic stretch increases splicing noise rate in cultured human fibroblasts
© Kaufmann et al; licensee BioMed Central Ltd. 2011
Received: 18 July 2011
Accepted: 31 October 2011
Published: 31 October 2011
Mechanical forces are known to alter the expression of genes, but it has so far not been reported whether they may influence the fidelity of nucleus-based processes. One experimental approach permitting to address this question is the application of cyclic stretch to cultured human fibroblasts. As a marker for the precision of nucleus-based processes, the number of errors that occur during co-transcriptional splicing can then be measured. This so-called splicing noise is found at low frequency in pre-mRNA splicing.
The amount of splicing noise was measured by RT-qPCR of seven exon skips from the test genes AATF, MAP3K11, NF1, PCGF2, POLR2A and RABAC1. In cells treated by altered uniaxial cyclic stretching for 18 h, a uniform and significant increase of splicing noise was found for all detectable exon skips.
Our data demonstrate that application of cyclic stretch to cultured fibroblasts correlates with a reduced transcriptional fidelity caused by increasing splicing noise.
Eukaryotic cells sense the physical properties of their microenvironment by translating mechanical forces into biochemical signals. This mechanotransduction and its triggered biological responses are crucial for the regulation of many important cellular functions [1–4]. Mechanical forces are also transmitted to the nucleus through the cytoskeleton by extra- or intracellular force generation [5–7]. Even though the nucleus is suggested to be stiffer than the surrounding cytoskeleton [8, 9], extracellular forces and strain result in clearly detectable deformations of the nucleus [5, 10] that can in turn induce conformational changes in chromatin organization and transcriptional regulation [11–14].
A common experimental approach permitting to investigate the effects of mechanical forces on cells in vitro is cyclic stretching of cultured cells plated on an expandable elastomeric substrate coated with extracellular matrix components such as fibronectin. The cells dynamically align their cell bodies and cytoskeletons in a direction perpendicular to the strain . The mean cell orientation changes exponentially with a frequency-dependent characteristic time from 1 to 5 h . Mechanisms involved in force-induced cellular reorganisation are focal-adhesion sliding, RhoA activation and the actomyosin machinery, whereas the process seems to be largely independent of the dynamic microtubule network [17, 18]. Together with the cells, their nuclei also become deformed [16, 19]. Numerous in vitro studies have shown that cyclic stretching alters the expression of several genes depending on the type of mechanical loading, stretching magnitude, frequency and duration . However, it is yet unknown whether the precision of nucleus-based processes is also influenced by cyclic stretching.
One method to determine the precision of nucleus-based processes is the detection of errors that occur during splicing (termed splicing noise) . A critical step in co-transcriptional splicing is the recognition and correct pairing of the 5' and 3' splice sites of the pre-mRNA by the spliceosome. The co-transcriptional assembly of the spliceosome in a stepwise manner around the splice site junctions requires the activity of several protein factors as well as five snRNAs [21, 22]. Splicing noise occurs if this process is disturbed, resulting for example in transcripts lacking one or more cassette exons. It was first detected in selected genes [22–26] and later suggested to be a more general process . More recently, it was shown in a genome-wide approach to occur at low frequency in almost all genes, with splicing noise rates of approximately 0.7% for the average intron . In vitro, splicing noise rates can be increased artificially by inhibiting the nonsense-mediated mRNA decay (NMD) or by culturing the cells at 20°C (cold shock) [22–24, 26].
In this work, splicing noise rates were investigated in cultured primary human fibroblasts exposed to uniaxial cyclic tensile strain with periodic alternation of the stretch direction every two hours. In the following, this condition was termed altered uniaxial cyclic stretch leading to continuous mechanical deformations of the cells. The amplitude and frequency of the cyclic stretch is related to the periodic strain induced by the pulsatile deformation of blood vessels .
A reliable and established method to measure splicing noise rates is the relative quantification of erroneous splice variants, such as variants lacking one cassette exon, compared to the wildtype product by RT-qPCR [22, 25]. Seven exon skip variants which have been found to be expressed in human fibroblasts were chosen out of several test genes: AATF (exon 3), MAP3K11 (exon 9), NF1 (exons 38 and 39), PCGF2 (exon 10), POLR2A (exon 23) and RABAC1 (exon 4). The detection method was validated by measuring increased splicing noise rate in cultured fibroblasts treated with cold shock.
Our study demonstrates that cyclic stretching in human fibroblasts is correlated to a reduced fidelity of a nucleus-based process by increasing the splicing noise rate in several genes.
Cell culture and preparation of the substrates
Tissue processing and preparation of human fibroblasts was performed as described . Biopsies from two healthy Caucasian male donors, K14 and K15 aged 11 and 9 years, were obtained from the prepuce. The research was carried out in compliance with the Helsinki Declaration, obtained written ethics approval from the ethics committee (Ethikkommission Universität Ulm, A 185/09) and written informal consent from all participants and their parents. Fibroblasts of early passages were cultured in Dulbecco's modified eagle medium with 10% fetal bovine serum at 37°C and 5% CO2 on cell culture flasks or polydimethylsiloxane (PDMS) substrates (Sylgard 184, Dow Corning, Midland Michigan, USA). The proliferation of cells was measured as described . For cold shock, fibroblasts were cultured for 24 h at 20°C . In the stretching and control experiments, the cells were cultured on PDMS substrates with an elastic modulus of about 1 MPa (data not shown). The chamber-like formed substrates with an adhesion surface of 20 × 20 mm were produced as described . In order to improve adhesion of the cells to the hydrophobic PDMS gel, chamber surfaces were treated with 70% Ethanol, washed with phosphate buffered saline and then coated with fetal bovine serum for 1 h at 37°C. Followed by two wash steps with phosphate buffered saline, the chambers were filled with cell culture medium prior to the seeding of the cells. Seeding was performed 48 h before the stretching experiment with a constant number of cells (n = 40 000 per chamber). The adhesion and distribution of the cells was examined 12 h later via light microscopy. Chambers with equally distributed cells were selected for cyclic stretching experiments to minimize effects of various cell densities.
Altered uniaxial cyclic stretching of cells
Uniaxial strain was applied with 8% amplitude and a frequency of 1 Hz with a change in stretch direction from x- to y-direction every two hours. The mechanical stimulation was performed by a customized stretching device equipped with two brushless servomotors (Faulhaber, Schoenaich, Germany) in an incubator at 37°C and 5% CO2. Stretching of the cells was performed overnight (18 hours) with the motors connected to a personal computer and controlled by Faulhaber Motion Manager 4 and Image Pro Plus 6 software (Media Cybernetics, Bethesda, USA) respectively. These conditions have previously been shown to be tolerable and non-toxic for human fibroblasts . Cells cultured on an unstretched PDMS substrate were used as control in the same incubator until the end of the experiment. Immediate RNA isolation out of the stretched cells and unstretched control cells followed.
RNA isolation and cDNA synthesis
Isolation of total RNA was accomplished using the RNeasy Mini Kit (Qiagen, Hilden, Germany) according to suggestions of minimum standards guidelines for fluorescence based qPCR experiments . Both the stretched substrate and the control substrate were put on ice immediately after the stretching experiment was stopped, and the cells were lysed through incubation with the kit's lysis buffer containing 1% 2-mercaptoethanol for 2 minutes. After using a cell scraper to scratch the lysed cells off the PDMS surface, the lysate was transferred to a Qiashredder spin column according to the manufacturer's protocol. Amount of RNA was determined by Nanodrop. The quality of RNA isolation was assessed by gel-electrophoretic separation of RNA samples and PCR on RNA to detect DNA contaminations using intronic NF1 primers. Reverse transcription of RNA to produce cDNA was performed using random hexamers together with the Superscript III Kit (Invitrogen, Karlsruhe, Germany).
Tested erroneous splice products
Structural data of the investigated transcripts.
AATF exon 3
MAP3K11 exon 9
NF1 exon 38
NF1 exon 39
PCGF2 exon 10
POLR2A exon 23
RABAC1 exon 4
Measuring splicing noise rates in qPCR
Primers used to detect skip and wildtype transcripts.
AATF S3 H
AATF S3 R
AATF WT H
AATF WT R
MAP3K11 S9 H1
MAP3K11 S9 R
MAP3K11 WT H
MAP3K11 WT R
NF1 S38 H
NF1 S38 R
NF1 S39 H
NF1 S39 R
NF1 WT H
NF1 WT R
PCGF2 S10 H1
PCGF2 S10 R1
PCGF2 WT H
PCGF2 WT R
POLR2A S23 H
POLR2A S23 R
POLR2A WT H
POLR2A WT R
RABAC1 S4 H
RABAC1 S4 R2
RABAC1 WT H1
RABAC1 WT R1
Reliable measuring of splicing noise rates in RT-qPCR
Relative occurrence of the exon skip transcripts (ΔCT) in cultured fibroblasts.
23.022 ± 0.130
39.630 ± 1.041
16.607 ± 1.049
24.228 ± 0.095
37.384 ± 0.041
13.156 ± 0.103
23.221 ± 0.083
27.377 ± 0.096
4.156 ± 0.127
22.615 ± 0.045
34.883 ± 0.220
12.267 ± 0.225
23.214 ± 0.201
38.793 ± 1.311
15.579 ± 1.326
24.408 ± 0.205
39.826 ± 0.350
15.419 ± 0.405
22.304 ± 0.131
29.750 ± 0.123
7.446 ± 0.180
Cyclic stretching of primary fibroblasts
The viability of the primary fibroblasts plated on the PDMS surface was observed by comparing the proliferation rates on both the PDMS surface and the culture flask surface showing no alteration. The cellular response to cyclic stretching was controlled by applying uniaxial cyclic strain (5 h, stretching frequency 1 s-1, amplitude 8%) whilst observing the cells by phase contrast light microscopy. A perpendicular orientation of cells relative to the stretching direction was observed. In unilaterally stretched cells the nuclei were deformed by about 4.8% as determined by measuring the circularities and the aspect ratios of the marked nuclei (data not shown). To test whether altered unilateral cyclic stretching with the applied parameters was tolerated by the primary fibroblasts, the RNA content of stretched cells and unstretched controls was compared. As a result, the total yield of RNA was within 1.6 and 4.1 μg/105 cells for both conditions, indicating that the applied stretching is a tolerable condition.
Increased splicing noise rates in altered uniaxial cyclically stretched cells
In this study, a uniform and significant increase in splicing noise was found for all detectable exon skips in fibroblasts treated by cyclic stretching. Similarly doubled splicing noise rates were found previously in spinal muscle atrophy (SMA) patient fibroblasts compared to control fibroblasts . SMA is commonly caused by the deletion of one of the two copies of the SMN gene, resulting in an insufficient expression of SMN, which is involved in the assembly of spliceosomal components, explaining the observed uniform increase in splicing noise rates. Therefore, it has to be assumed that consistently doubled splicing noise rates indeed exert an in vivo effect with presumable clinical relevance. Given a certain basic error rate per splicing reaction, it can further be assumed that genes with a higher number of introns bear less functional wild type transcripts and therefore should be more affected by uniformly increased splicing noise rates. This could be especially meaningful if a tightly balanced gene dose is inevitable, such as for tumor suppressor genes . On the other hand, several proteins involved in the RNA surveillance mechanism NMD which has to cope with splicing noise also play roles in cell cycle progression or telomerase maintenance, and NMD is becoming more and more understood as a regulated process which additionally alters the expression of alternatively spliced isoforms as well as being involved in tumorigenesis . It could thus be interesting to investigate the influences of increased splicing noise rates on NMD in future studies.
Most human cells in vivo are continuously exposed to external forces as per those due to the periodic strain induced by the pulsatile deformation of blood vessels. Cyclic stretching of cultured fibroblasts on PDMS substrates can be one experimental approach to investigate cellular responses to such periodic forces and has been applied in various studies investigating the mechanoregulation of gene expression . Nuclear deformations can influence transcriptional regulation [12, 33]. However, the mechanism by which nucleus deformation induces altered gene expression is still unknown. It has been suggested that nucleus deformation influences the positioning of chromosomes mechanically linked to components of the inner nuclear membrane . Mechanical forces thus may also influence chromatin structure and in particular nucleosome positioning . Varying stretching amplitudes and frequencies have been observed in a previous study concerning the cell's dynamic reorientation behaviour . In this regard, it would be interesting in a follow-up study to check whether variations of the applied stretching parameters correlate with the resulting amount of splicing noise. Moreover, the recent identification of the two transcriptional regulators YAP and TAZ should give additional molecular insight because of their involvement in mediating biological responses to mechanical inputs such as variations of extracellular stiffness or changes in cell shape .
Here we chose to investigate a different effect of cyclic stretching on nuclear function, namely the precision of a nucleus-based process. We analysed the error rates in co-transcriptional splicing of several test genes as detected by RT-qPCR. This approach was proved to be a sensitive and reliable method for detecting differences in splicing noise rates in small amounts of primary cells [22, 31]. As demonstrated recently in a genome wide approach, splicing noise is a general process . Therefore, test genes and exons could be selected more or less stochastically.
The quite uniform increase in splicing noise we found in these few genes most probably represents a general trend. However, a more systematic and expensive approach will be helpful to further confirm the effects of cyclic stretching on splicing noise rates such as a genome wide deep cDNA sequencing.
As to the cause of the increased splicing noise rates in cyclically stretched cells, a possible direct effect influenced by the mechanical deformation of the nucleus still has to be further validated in the following. One possible strategy to support this idea would be to disrupt cytoskeletal structures physically linking the nucleus to the periphery. In addition, it would be informative to find out whether the observed effects on transcription fidelity are related to the activation of some heat shock proteins such as hsp-72 or hsp-90 [37, 38] or to the expression of YAP or TAZ . Until now, there are no evidences that the expression of these genes influences splicing noise rates. Finally, the observed general increase in splicing noise rates in cyclically stretched cultured fibroblasts raises the question of its physiological relevance. Minding the fact that some body cells are subjected to the periodic strain, the described experimental conditions could indeed resemble the cell's physiological environment better than standard cell culture conditions. Hence, further observation of splicing noise rates in other cell types such as endothelial cells, could give greater insight into co-transcriptional fidelity in different cell types or even tissues.
In summary, the described work represents the first examination on the effects of cyclic stretching of cultured cells on splicing noise rates. In the selected genes, a uniform significant increase was found in cultured human fibroblasts.
The technical support of A. Schwandt is gratefully acknowledged. We thank S. Biewener for the contribution in discussing the topic, J. Hoegel for statistical investigations, K. Kaempchen for correcting the manuscript and M. Kalafat, T. Busch for their continuous and friendly support.
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