- Open Access
Transfection of the mutant MYH9 cDNA reproduces the most typical cellular phenotype of MYH9-related disease in different cell lines
© Panza et al; licensee BioMed Central Ltd. 2008
- Received: 30 May 2008
- Accepted: 01 December 2008
- Published: 01 December 2008
Heterozygous mutations of MYH9, encoding the Non-Muscular Myosin Heavy Chain-IIA (NMMHC-IIA), cause a complex disorder named MYH9-related disease, characterized by a combination of different phenotypic features. At birth, patients present platelet macrocytosis, thrombocytopenia and leukocyte inclusions containing NMMHC-IIA. Moreover, later in life some of them develop the additional features of sensorineural hearing loss, cataracts and/or glomerulonephritis that sometimes leads to end stage renal failure.
To clarify the mechanism by which the mutant NMMHC-IIA could cause phenotypic anomalies at the cellular level, we examined the effect of transfection of the full-length mutated D1424H MYH9 cDNAs. We have observed, by confocal microscopy, abnormal distribution of the protein and formation of rod-like aggregates reminiscent of the leukocyte inclusions found in patients. Co-transfection of differently labeled wild-type and mutant full-length cDNAs showed the simultaneous presence of both forms of the protein in the intracellular aggregates.
These findings suggest that the NMMHC-IIA mutated in position 1424 is able to interact with the WT form in living cells, despite part of the mutant protein precipitates in non-functional aggregates. Transfection of the entire WT or mutant MYH9 in cell lines represents a powerful experimental model to investigate consequences of MYH9 mutations.
- Sensorineural Hearing Loss
- MYH9 Mutation
- Confocal Laser Scanning Microscopy System
- Laser Scanning Microscopy System
- attB2 Recombination Site
Heterozygous mutations in the MYH9 gene, encoding the Non-Muscle Myosin Heavy Chain IIA (NMMHC-IIA), are responsible for the recently defined MYH9-related disease (MYH9-RD) . This entity includes clinical phenotypes previously classified as distinct disorders: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome. All patients present since birth thrombocytopenia and leukocyte inclusions consisting of aggregates of NMMHC-IIA. However, during infancy or adult life many subjects develop the additional features of sensorineural hearing loss, cataracts, and/or progressive nephropathy leading to renal failure .
NMMHC-IIA is a conventional, non-sarcomeric myosin expressed in most cells and tissues, where it is involved in several functions including cytokinesis, cell motility, and maintenance of cell shape . The N-terminal portion of NMMHC-IIA forms the myosin globular head, responsible for ATPase and actin-binding activity, while the C-terminal tail region regulates both dimerization of heavy chains in coiled-coil structures and association of myosin molecules into functional filaments .
The mechanisms by which MYH9 mutations cause MYH9-RD are poorly defined, and both haploinsufficiency and a dominant-negative effect of the mutated protein have been hypothesized [3–6]. In particular, studies on NMMHC-IIA tail fragments demonstrated that differently mutated proteins could interact to a different extent with WT counterparts to exert a dominant-negative biochemical effect . Nevertheless, investigations on megakaryocytes and platelets from patients with MYH9-RD suggested that mutant NMMHC-IIA proteins could not be expressed in living cells, possibly because of their high instability [3, 6]. Difficulties in addressing these issues include the unavailability of the entire NMMHC-IIA , so that experimental approaches were so far limited to in vitro studies on either N-terminal or C-terminal portions of the molecule .
Here we present the results of transfection with the entire NMMHC-IIA molecule both in wild-type (WT) and mutated form (D1424H) in COS-7 and HeLa cell lines.
The full-length 5883 bp MYH9 cDNA was cloned using the Gateway system (Invitrogen). RNA was extracted from a lymphoblastoid cell line from a control individual. Five hundred nanograms of total RNA were specifically retrotranscribed in order to obtain MYH9 cDNA (Transcriptor First Strand cDNA Synthesis Kit, Roche). The resulting cDNA was used for PCR amplification. Primers, which included the attB1 and attB2 recombination sites, were:
Forty nanograms of cDNA were used to amplify the entire MYH9 coding sequence.
The PCR fragment was introduced into plasmid vector pDONOR207 (Invitrogen) via the BP recombination reaction, according to the recommendations of the manufacturer, to generate the entry clone. Control of the resulting cDNA was performed by complete sequencing. Comparison of the sequence in our clone with the cDNA reported in the NCBI database (NM_002473) did not reveal any difference.
Site directed mutagenesis was performed using a commercial kit (Quick Change, Stratagene) to introduce a G to C transversion in position 4270, in order to obtain the D1424H mutant. WT and D1424H constructs were then used to perform LR recombination reactions with the Gateway system compatible expression vector pcDNA3.1/nV5-DEST (Invitrogen) and Gateway converted Flag vector to express N-terminally tagged V5, or Flag fusion proteins, respectively. The integrity of all constructs was confirmed by direct complete DNA sequencing.
COS-7 and HeLa cells were maintained in Dulbecco's modified Eagle's medium supplemented with 10% (v/v) fetal bovine serum (GibcoBRL), 2 mM L-glutamine, 100 U/ml penicillin, 100 μg/ml streptomycin at 37°C in a humidified atmosphere with 5% CO2. Transfections of both cell lines were performed using the Polyfect reagent (Quiagen), according to the manufacturer's instructions, on cells plated at 50–60% confluence and transfected at an estimated 80–90% confluence after 24 h. Cells were harvested 24, 48 and 72 hours after transfection and cytospun onto slides for immunofluorescence staining.
Standard peripheral blood smears were prepared from two patients with MYH9-RD caused by D1424H substitution of NMMHC-IIA. Both patients have been already reported . The institutional review board of Fondazione IRCCS Policlinico San Matteo, University of Pavia, Italy, approved the study and patients gave written informed consent to the study.
The following primary antibodies (Abs) were used: rabbit polyclonal PR-B440P (Covance Research Products Berkeley, CA) recognizing the 12-residues sequence (GKADGAEAKPAE) of the C-terminus of NMMHC-IIA , mouse monoclonal NMG2 to a specific epitope of the N-terminus of NMMHC-IIA (a kind gift of Dr Saverio Sartore, Biomedical Sciences, University of Padua, Italy) ; rabbit polyclonal anti-flag (Sigma, St. Louis, MI), and mouse monoclonal anti-V5 (Invitrogen).
Secondary antibodies were goat anti-mouse or anti-rabbit conjugated with either Alexa Fluor 488 or Alexa Fluor 594 (Invitrogen). Confocal microscopy was performed through the TCS SPII confocal laser scanning microscopy system (Leica, Heidelberg, Germany), equipped with a Leica DM IRBE inverted microscope, as previously described . Confocal optical sections were performed every 500 nm. Conventional fluorescence microscopy was performed through an Axioscope 2 Plus microscope (Carl Zeiss, Gottingen, Germany), as described .
The entire 5883 bp MYH9 cDNAs, both WT and D1424H form, have been transfected in COS-7 or in HeLa cell lines. Immunofluorescence staining showed that COS-7 cells, which constitutively do not express MYH9, expressed the transfected WT or D1424H NMMHC-IIAs, and that the signal of these molecules was stable for at least 72 hours after transfection. No NMMHC-IIA signal has been observed in non-transfected cells or in cells transfected with the vector alone. Transfected COS-7 cells were similarly labeled by antibodies specific either to the N-terminus or to the C-terminus of the protein, demonstrating that the entire WT or mutant NMMHC-IIA were expressed.
These aggregates of mutant NMMHC-IIA were present in most transfected cells, and they were usually evident over a diffuse cytoplasmic staining. When we transfected with the same constructs HeLa cells, which constitutively express NMMHC-IIA, we obtained the same results as in COS-7 (Figure 1C).
Thus, transfection of the entire MYH9 mutant cDNA reproduced in two different cell lines, independently from their endogenous myosin expression, the NMMHC-IIA aggregates that are typical of granulocytic cells in MYH9-RD [1, 4, 10]. Interestingly, a similar distribution of NMMHC-IIA was observed in tubular epithelia cells from the only patient with MYH9-RD whose renal biopsy was investigated by immunohystochemistry , suggesting that this behavior of mutant NMMHC-IIA could be common to different cell types in vivo.
Results of cotransfection similar to those in COS-7 cells were also obtained in HeLa cells (not shown).
These findings suggest that the NMMHC-IIA mutated in position 1424 is able to interact with the WT form in living cells, despite part of the mutant protein precipitates in non-functional aggregates. This observation is consistent with previous studies on an in vitro model, which demonstrated that the D1424N C-terminal fragment of NMMHC-IIA, when mixed with its WT counterpart, is able to form paracrystalline assemblies similar to those of the WT/WT interaction . The fact that NMMHC-IIA mutated in position 1424 retains the ability to interact with WT protein represents the basis for it to exert a dominant-negative biochemical effect on the normal protein.
Transfection of the entire WT or mutant MYH9 in cell lines represents a promising experimental model to investigate consequences of MYH9 mutations in cells.
The research was supported by a grant for Rare Diseases from the Istituto Superiore di Sanità, Ministry of Health, Italy.
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