Ku86 exists as both a full-length and a protease-sensitive natural variant in multiple myeloma cells
© Gullo et al; licensee BioMed Central Ltd. 2008
Received: 16 November 2007
Accepted: 29 April 2008
Published: 29 April 2008
Truncated variants of Ku86 protein have previously been detected in 86% to 100% of freshly isolated patient multiple myeloma (MM) cells. Since, the Ku70/Ku86 heterodimer functions as the regulatory subunit of the DNA repair enzyme, DNA-dependent protein kinase, we have been interested in the altered expression and function of Ku86 variant (Ku86v) proteins in genome maintenance of MM.
Although, a number of studies have suggested that truncated forms of Ku proteins could be artificially generated by proteolytic degradation in vitro in human lymphocytes, we now show using whole cell immunoblotting that the RPMI-8226 and SGH-MM5 human MM cell lines consistently express full-length Ku86 as well as a 69-kDa Ku86v; a C-terminus truncated 69-kDa variant Ku86 protein. In contrast, Ku86v proteins were not detected in the freshly isolated lymphocytes as was previously reported. Data also indicates that the Ku86v was not generated as a result of carbohydrate modification but that serine proteases may act on the full-length form of the protein.
These data confirm that MM cells contain bona fide Ku86v proteins that were generated intracellularly by a post-transcriptional mechanism, which required proteolytic processing.
Ku80 and Ku70 are two important related family members involved in the facilitation of DNA double strand break repair (DSBR) in association with the DNA repair enzyme, the catalytic subunit of DNA-dependent protein kinase catalytic (DNA-PKcs), XRCC4, DNA ligase IV and a host of other enzymes. Although present in most cells, Ku86 has been extensively studied in B and T cells due to its proposed role in the CD40-induced immunoglobulin (Ig) class switch recombination (CSR) and V(D)J lymphocyte antigen recognition/recombination events, both of which generate transient DNA double-strand breaks. The importance of this protein in lymphocyte development was most notable in Ku86 knockout mice, which failed to develop mature lymphocytes . There has also been a strong association with Ku-dependent DNA DSBR and/or protection from ionizing irradiation-induced DNA damage [2–6]. Besides its well known role in DNA repair, numerous reports have implicated Ku proteins in numerous other cellular processes, including the maintenance of telomere length, regulation of G2 and M phases of the cell cycle, regulation of apoptosis and specific gene transcription, and regulation of heat shock-induced responses [7, 8].
Although Ku86 and Ku70 are predominantly localized to the nucleus and the nuclear matrix, it has been found in other subcellular compartments including the cytoplasm  and cell membranes of numerous cell types [10, 11]. The identification of Ku proteins in various compartments of the cell has led to the identification of putative novel functions of both Ku86 and Ku70. For example, in multiple myeloma (MM) cells, CD40-induced Ku86 surface expression resulted in increased cellular adhesion to fibronectin and bone marrow stromal cells  Other reports indicate that Ku70/Ku86 is found in the cytoplasm during mitosis and it returns to the nucleus as the cell enters the G1 phase of the cell cycle [13, 14]. Finally, in colonic tumor cells, translocation of Ku86 from the cytoplasm to the nucleus occurs via interactions with a growth inhibitory tetradecapeptide and thus, Ku86 acts as a putative somatostatin receptor . Therefore, location of Ku86 and other members of the DNA repair machinery in various compartments of mammalian cells may lead to numerous downstream functional consequences.
There have been a number of reports that indicate Ku86 exists in two forms, an 86 kDa full-length form and a C-terminal truncated variant form of approximately 69-kDa, in B cells from the peripheral blood (PB) , the acute promyelocytic leukemia (APL) cell line HL-60 , MM cells , as well as senescent fibroblasts . It is unlikely that the variant protein is a product of alternative splicing of the Ku86 full length transcripts since shorter mRNAs have not been found by northern blot analysis [16, 17]. Consistent with these findings, a 69-kDa variant of Ku86 was also found in the mitochondria of mammalian cells . Furthermore, in the above reports, the variant of Ku86 was still able to bind DNA and associate with Ku70 consistent with the retention of the domains that are associated with those functions. Therefore, it is currently thought that variants of Ku86 are formed as a result of post-translational modification. It is the nature of this modification, which has resulted in some controversial issues regarding the physiological existence of this variant. Several recent studies have suggested that the Ku86 variant seen in lymphocytes may be due to cleavage by proteases induced during biochemical isolation [20–22]. Considering the increased amount of genomic instability seen in MM, the disregulated CD40/interleukin-4 (IL-4) pathway in MM cells , and the role of Ku in DNA DSBR and non-homologous end-joining (NHEJ), we investigated the presence of Ku86 and its variants in MM cells, and compared them to T lymphocytes and other cell lines. We found that unlike human T lymphocytes, the detection of 69-kDa Ku86 (Ku86v-N) variant is not likely due to in vitro generated protease cleavage. Moreover, we demonstrate that the full-length, as well as the truncated form of Ku86 are found in the nucleus, membrane and cytosolic fractions of resting and CD40-stimulated MM cells. Finally, we show that intracellular protease inhibition can prevent the appearance of the Ku86 variant and that the protease responsible is likely to be a serine protease. The implications for these findings are discussed.
RPMI 8226 MM, CESS Epstein-Barr virus (EBV)-transformed normal B cells, K562 chronic myeloid leukemia (CML), and HL-60 APL human cell lines were all purchased from the American Type Culture Collection (ATCC, Rockville, MD). The EBV-negative SGH-MM5 human MM cell line (CD10+ CD19- CD20- CD38+ CD40+ CD45+ CD56+ CD138+) was developed in our laboratory under the Singapore General Hospital (SGH) Institutional Review Board (IRB) good research practice guidelines, from a patient with MM using a modified Dexter-type long-term tissue culture system, which was previously described . All cell lines were cultured in RPMI 1640 medium (Invitrogen, Gibco, Grand Island, NY) supplemented with 10% fetal calf serum (FCS) at 37°C and 5% CO2. Normal PB human T cells were isolated from buffy coat preparations from healthy donors (after informed consents were obtained) using Ficoll Hypaque density gradient centrifugation and CD3 positive magnetic bead immunoseparation (MACS columns, Miltenyi Biotec, GmbH, Gladbach, Germany). For CD40 stimulation conditions, MM cells were optimally stimulated with soluble CD40 ligand (sCD40L) (Peprotech Inc., Rocky Hill, NJ) for 4 hrs at 5.0 ng/mL .
Cell extract preparation
Fresh whole cell extracts
Cells were washed in phosphate buffered saline (PBS), pelleted, resuspended in 2× sodium dodecyl-sulfate (SDS) loading buffer (120 mM Tris HCl pH 7.0, 4% SDS, 720 mM 2-mercaptoethanol (2-ME), 0.01% bromophenol blue and 20% glycerol), and directly boiled for 10 mins to inactivate proteases  as previously described. Whole cell extracts were then recovered by centrifugation at 12,000 g for 10 mins and loaded equally and immediately onto SDS polyacrylamide gel electrophoresis (PAGE) gels.
Conventional whole cell extracts
Cells were lysed in EBC1 lysis buffer (50 mM Tris HCl, pH 8.0, 150 mM NaCl, 0.1% NP-40, 50 mM NaF, 1 mM Na3VO4, 0.5 μg/ml phenylmethylsulphonylfluoride (PMSF), and 1 freshly added tablet of protease inhibitor mixture per 50 ml of buffer (Complete™ protease inhibitor tablets; Boehringer Mannheim, Roche Diagnostics GmbH, Mannheim, Germany). The mixture was then boiled in SDS sample buffer for 3 to 5 mins before loading onto SDS-PAGE gels.
Conventional cytosolic protein extracts
Cells were first washed in PBS and lysed in 10 volumes of the lysis buffer (10 mM Tris HCl pH 7.6, 1.5 mM MgCl2, 10 mM KCl, 0.5% NP-40, 1 mM dithiotretinol (DTT), and 1 freshly added Complete™ protease inhibitor tablet). Cytosolic protein extracts were recovered by centrifugation at 1,000 g for 15 mins .
Conventional nuclear protein extracts
From the above pellet, cell nuclei were next lysed in 5 volumes of a low-salt buffer (20 mM HEPES pH 7.9, 25% glycerol, 1.5 mM MgCl2, 10 mM KCl, 0.5 mM ethylenediaminetetraacetic acid (EDTA), and 1 freshly added Complete™ protease inhibitor tablet). Next, an equal volume of a high-salt buffer (i.e. low-salt buffer plus 0.8 M NaCl) was added, and the mixture left to stand on ice for 15 mins. . Nuclear protein extracts were recovered by centrifugation at 16,000 g for 15 mins.
Membrane protein extracts
Cells were washed three times with ice-cold PBS, centrifuged at 3,000 g for 5 mins, and the pellet resuspended in 0.5 ml of TEM A lysis buffer (20 mM Tris HCl pH 8.0, 0.5 mM EDTA, 0.5 mM EGTA, 10 mM 2-ME, and 1 freshly added Complete™ protease inhibitor tablet), incubated on ice for 5 mins, and then sonicated. Membrane protein extracts were obtained by double sequential centrifugation of the lysis mixture, first at 1,000 g for 5 mins, then at 100,000 g for 30 mins for 250 μL of the supernatant. For all the assays above, Bradford's assay (Bio-Rad, Hercules, CA) was used to quantify protein concentrations in all samples.
Cell lysates (20.0 μg of protein/sample) were first resolved on a 12.5% SDS-PAGE gel, transferred onto polyvinylidene difluoride (PVDF) membranes (Millipore Corporation, Billerica, MA) and then blocked using Tris buffered saline Tween-20 (TBST) buffer containing 5% non-fat milk. Membranes were next hybridized overnight in the cold room using various murine monoclonal antibodies (mAb) – i.e. S10B1 anti-Ku86 N-terminus (amino acid (aa) residues 8–221; NeoMarkers, Fremont, CA); anti-heavy chain of the human major histocompatibility complex (MHC) mAb (clone 22.63.4, Accurate Chemical and Scientific Co., Westbuty, NY; a kind gift from P. Macary, from the National University of Singapore); and anti-actin (Santa Cruz Biotechnology, Santa Cruz, CA) mAbs; washed three times in ice cold TBS-T; and then incubated with horseradish peroxidase (hrp) conjugated anti-mouse IgG mAb (1:2,000; Santa Cruz) for 1 hr. The reaction was detected using the ChemiGlow chemiluminescence reagents (Alpha Innotech, San Leandra, CA). Image spot densitometry was performed on the Alpha Imager (Alpha Innotech).
Electrophoretic mobility shift assay (EMSA)
Two 25-mer oligonucleotides; 5'-ACTTGATTAGTTACGTAACGTTATG-3' and 5'-CATAACGTTACGTAACTAATCAAGT-3', with or without biotin labels at the 5' ends (1st Base Pte Ltd., Singapore), were first annealed together (see Pierce Technical Resource, TR0045.0, Pierce, Rockford, IL). Standard EMSA reactions (Lightshift Chemiluminescent EMSA kit, Pierce) incorporated 4.0 μg of cell extract and 20.0 fmol of biotin end-labeled DNA in a 20.0 μL volume binding reaction in the presence of 2.5% glycerol, 5 mM MgCl2, 50 ng/μL of poly(dI·dC), and 0.05% NP-40. Unlabeled target DNA (4.0 pmol) was added per 20.0 μL of binding reaction where indicated. Reactions were incubated at room temperature for 30 mins and terminated by adding 2.0 μL of 10× loading buffer (0.2% (w/v) bromophenol blue and 0.2% xylene cyanol containing 10% (v/v) glycerol). Assays were loaded onto native 5% polyacrylamide gels that were pre-electrophoresed for 60 mins in 0.5× Tris borate/EDTA buffer, resolved at 100 V, and transferred onto nylon membranes (Hybond™-N+, Amersham) in 0.5× Tris borate/EDTA buffer at 100 V for 30 mins. DNA was cross-linked (120 mJ/cm2) and detected using hrp-conjugated streptavidin chemiluminescence. Image spot densitometry was performed on the Alpha Imager (Alpha Innotech).
Endoglycosidase H (EndoH) digestion
Endoglycosidase H resistance was assayed using the EndoH digestion system (New England Biolabs, Ipswich, MA) and performed according to the manufacturer's recommendations. Briefly, 30.0 μg of whole cell extracts were denatured at 100°C for 10 mins using 1× glycoprotein denaturing buffer, followed by addition of 1× G5 buffer and 1.0 μL (500 units) of EndoH. The reaction mix was incubated at 37°C; and at various time points, aliquots were removed and resolved in a 12.5% SDS-PAGE gel for carbohydrate (CHO) release.
Intracellular inhibition of protease digestion
In order to inhibit intracellular protease activity, 5 × 106 cells/sample were treated with: Complete™ protease inhibitor tablets; either 1× (1 tablet for every 50 mL of media) or 2× (2 tablets for every 50 mL of media); or treated with antipain (2.0 μg/mL) plus leupeptin (2.0 μg/mL) (both from Sigma-Aldrich, St Louis, MO, USA) for cysteine protease inhibition; or aprotinin (2.0 μg/mL) plus PMSF (100 μg/mL) (both from Sigma-Aldrich) for serine protease inhibition; for to 24 hrs. Cell viability was assessed by standard trypan-blue exclusion assays. Image spot densitometry was performed on the Alpha Imager (Alpha Innotech).
Cloning of Human Ku86 from RPMI cells
Full-length 2.4 kb Ku86 cDNA was obtained from total RNA of RPMI 8226 MM cell lines by RT-PCR (Qiagen Inc., Valencia CA, USA). The primers used to amplify the Ku86 message were forward primer: 5' -TGTATGGACGTGGGCTTTACCAT-3' and reverse primer: 5' -TCCACAGAGAATTAGATGATCCGCC-3'. Purified Ku86 cDNA (2.4 kb) was then cloned into Topo-vector (Invitrogen) and transformed into E. coli. The cloned Ku86 gene was fully sequenced to confirm the insertion of full length 2.4 kb Ku86 into the clone without any detected mutations (BigDye™ Cycle Sequencing Kit, Applied Biosystems, Foster City, CA USA). In order to subclone the construct into an mammalian expression system, two restriction enzyme sites were engineered to the ends of cloned Ku86 gene (Hin dIII at 5' end and Xba I at 3' end) by PCR of the clone using high fidelity PWO SuperYield™ DNA polymerase (Roche Diagnostics) and the following oligo's: Forward oligo: 5'-ATTAAAGCTTCCGGCAACATGGTGCGGTCGGGGAATAAGGCAGCTGTTGTGCTGTGTATGGACGTGGGC-3' and Reverse oligo: 5'ATTATCTAGACTTATCATGTCCAATA AATC-3'. The engineered Ku86 was then subcloned into the transient mammalian expression vector, pcDNA3.1/myc-His B (Invitrogen). The purified plasmid (Ku86+ pcDNA3.1/myc-His B) was then transfected into mammalian cell line (COS-7) for transient expression of Ku86 recombinant protein, using the Lipofectamine 2000™ reagent (Invitrogen). Finally, the Ku86 recombinant proteins were purified using ProBond™ Nickel-Chelating Resin column (Invitrogen) and detected using western Immunblotting with anti-myc-HRP (Invitrogen) and/or anti-Ku86 antibody (Neomarker).
Trypsin digestion of recombinant human Ku86 (rhKu86) protein
Full-length rhKu86 was first expressed and purified from COS cells and digested (6.5 μg/sample or 13.0 μg/sample) using trypsin (0.065 μg of Trypsin Gold/reaction, Promega Corp. Madison, WI); at 100:1 protease:protein ratio, in 50 nM acetic acid, pH 8.0, and 37°C, as recommended at by the manufacturer (Promega Technical Bulletin, 309). The reaction was stopped by rapid freezing on ice, and analyzed using SDS-PAGE and western immunoblotting.
Results and Discussion
Ku86 truncation is not the result of in vitro generated proteolysis in MM cell lines
In order to demonstrate in vitro proteolysis of Ku86, we next analyzed protein extracts prepared using conventional methods from previously frozen and stored cells (Fig. 1B). Specifically, human T cells (samples from patients 2 and 3), CESS and the K562 cell lines, that lack 69-kDa Ku86v expression (Fig. 1B, lanes 1 to 4); were compared with the HL-60 cell line, which is known to express 69-kDa Ku86v, RPMI 8226, and SGH-MM5 MM cell lines (Fig. 1B, lanes 5 to 7). In this experiment, both human T cells, as well as the CESS and K562 cell lines not only contained 69-kDa Ku86v, but also various other fragments of Ku86. Moreover, even HL-60, RPMI 8226 and SGH-MM5 cell lines, that constitutively express 69-kDa Ku86v, also contained numerous Ku86 fragments. These data suggest that freezing and storage of cells leads to extensive in vitro proteolysis of cellular proteins. Furthermore, whole cell extracts from the RPMI 8226 cell line, which were made in a protease-free extraction buffer, i.e. either extraction buffer plus 1× Complete™ tablet (Roche Diagnostics) and 1× PMSF, or extraction buffer plus 2× Complete™ tablets and 2× PMSF, demonstrated no change in the expression of the Ku86 variant or its full-length form (data not shown). Collectively, these data confirm that although proteases released during isolation procedures can lead to extensive Ku86 degradation in vitro, truncated forms of Ku86 in RPMI 8226 and SGH-MM5 MM cell lines are more likely to have been generated in vivo and constitutively.
The 69-kDa Ku86v in MM cell lines are present in the cytosolic, nuclear and membrane fractions and binds DNA
Surprisingly, triggering of MM cells via CD40 had no effect on the amount of 86-kDa Ku86 protein bound to DNA in all cellular subfractions (Fig. 2B, band position I) isolated from RPMI 8226 cells and well as SGH-MM5 MM cell line (data not shown). By contrast, binding of 69-kDa Ku86v to DNA was constitutively greater in the cytosol and cell membrane, but not in the nucleus (Fig. 2B, band position II); suggesting that 69-kDa Ku86v could be functionally different in different cellular compartments. Binding of DNA to 69-kDa Ku86v in both the cytosol and cell membrane is increased following CD40 triggering of RPMI 8226 MM cell lines; suggesting that CD40 triggering could induce the DNA-binding activity of Ku86v. This increased binding following CD40 triggering is not accompanied by increased amount of Ku86v expression in the nuclear fraction, as the levels are similar before and after CD40 triggering (Fig. 2A). Whereas this appears to be true for cell membrane Ku86v, expression of 69-kDa Ku86v in the cytosol is increased by approximately 2.5-fold after CD40 triggering (Fig. 2A), suggesting that increased sequestration or recruitment of 69-kDa Ku86v to the cytosol, rather than an increase in the DNA-binding activity of Ku86v, could be the more probable reason for these observations. This data is in contrast to a previously published report that shows a predominant Ku86 variant DNA-binding complex in nuclear extracts of human lymphocytes  and suggests that MM cells have a unique pattern of Ku86 distribution.
69-kDa Ku86v in MM cell lines is not the result of alternative splicing of RNA or post-translational modification by N-linked deglycosylation
Proteolysis plays an important role in the intracellular generation of 69-kDa Ku86v in MM cell lines
Trypsin generates a 69-kDa Ku86 variant protein from a full-length cloned human MM Ku86 protein (rhKu86) in vitro
Karyotypic analysis of tumor cells from patients with MM, as well as MM cell lines, frequently demonstrates numerous complex chromosomal abnormalities. Moreover, new chromosomal translocations into the switch region of the immunoglobulin heavy chain (IgH) gene (chromosome 14q32) often heralds transformation to more aggressive MM  Since DNA DSBR is important in mediating these processes, this suggests that abnormalities in DSBR could ultimately lead to genomic instability, clonal evolution and disease progression in MM. Truncated variants of Ku86 protein (i.e. Ku86v) have previously been detected in 86% to 100% of freshly isolated patient MM cells . However, since the expression of an altered form of the Ku86 protein in B cells  has been recently challenged . as perhaps being non-physiological, we carefully investigated the presence of truncated forms of Ku86. The presence of the 69-kDa truncated form of Ku86 detected by antibodies directed against the N-terminus part of the protein was confirmed in both traditional western blots as well as direct lysate fresh whole cell western immunoblotting.
In agreement with previously published data that the C-terminus truncated Ku86 variant from MM cells binds double stranded DNA ends , we show DNA end-binding (DEB) activity with both the full-length and truncated variant of Ku86 in all cellular subfractions tested. This is consistent with the 69-kDa variant of Ku86 that was found in mammalian mitochondria that still associates with DNA and is found in a complex with Ku70 . Since the DNA binding motifs of Ku86 are located in the N-terminus, and the functional domains are located in the C-terminus, these data support the notion that while Ku86v-C binds DNA, it is in fact incapable of regulating DNA repair. This is further supported by published data that demonstrated the heteroduplex of Ku70 and Ku86 variant bind DNA-PKcs less well than those containing full-length Ku86  and are deficient in DNA-PK activity . The link between the defective DNA-PK activity as a result of Ku86 variant and Ku70 heteroduplex formation and genomic instability in MM has not been proven thus far, although cells expressing Ku86 variants do display increased sensitivity to DNA damage [5, 16, 17]. The ability of multiple myeloma-specific Ku86 variant protein to bind Ku70 or itself and to activate DNA-PK and its overall effect on DNA repair in MM cells is the subject of ongoing work.
Since protease digestion of DNA-PK and Ku proteins are enhanced by proteasome inhibition (i.e. bortezomib treatment) in MM cell lines  these data taken in aggregate further suggest that proteolytic enzymes that are capable of digesting Ku proteins are constitutively activated, and possibly accumulate and/or become further activated under proteasome inhibition in MM cells. Thus, the observed trypsin-like serine protease-dependent cleavage of Ku86 during the isolation procedures  may in fact operate naturally in intact MM cells. These findings, as well as those that found that modification of Ku86 can occur with viral infections, phorbyl ester, and calcium phosphate treatment in CV1 cells , suggest that under certain conditions or in certain cells lines Ku86 truncation may occur in a non-inducible proteolytic-dependent fashion. Our data suggests that these potential proteases may be acting in the cell naturally and perhaps in a constitutive fashion in MM cells. Serine protease inhibition is much more effective than cysteine protease inhibition in reducing the appearance of the Ku86 variant in whole RPMI cells (Fig. 4B). Using rhKu86 and in vitro limited digestion, one likely candidate may be trypsin (Fig. 5). In fact, by looking at the sequence of Ku86 and using bioinformatics approach we were able to narrow down potential digestion of Ku86 into 20 different proteases (using the Peptide Cutter Peptide Characterization software- ExPASy, Swiss Institute for Bioinformatics). Trypsin, chymotrypsin and other serine proteases putatively cleave Ku86 in multiple locations. However, finding the exact physiologically relevant protease that generates the variant in vivo will require more detailed analysis. We have only partially attempted to address this by using protease inhibitor in living cells. At the doses used, antipain and leupeptin are more selective towards cysteine inhibition than towards inhibition of serine proteases and aprotinin and PMSF are powerful serine protease inhibitors. However, it is important to note that there is likely to be some cross-inhibition. Thus, other studies using various single and multiple cysteine and serine protease inhibitors as well as mettaloproteinase inhibitors such as TIMP-2, will be needed to more closely address this issue. However, this study as well as two others, [18, 22] suggest that serine proteases are likely to be important for the generation of the 69-kDa form of Ku86. However, our studies as well as others investigate Ku86 and its variant in conditions that do not allow for the association with Ku70. It is well known that Ku86 is most effective in binding DNA and recruiting DNA repair enzymes when it is heterodimerized with Ku70 which occurs via the C-terminus of both proteins . We are interested in determining the naturally occurring proteolytic cleavage site of Ku86 and to examine how it affects hetero-complex formation. We hypothesize that a fraction of newly synthesized Ku86 protein is immediately and constitutively cleaved by proteases into a Ku86 69-kDa form that would prevent it from tight association with Ku70.
The localization of Ku86 within different compartments within the cell is likely to be of significant importance in B cell DNA repair and perhaps in the regulation of genomic stability of MM cells. In fact, the intracellular trafficking of Ku protein to extranuclear sites has been suggested to play important role in numerous non-DNA repair Ku-associated functions [7, 13] Importantly, the localization of Ku to the membranes of MM cells following sCD40L treatment leads to increased adhesion to bone marrow stromal cells and interneukin-6 (IL-6) production . These and other studies prompted us to thoroughly examine the localization of Ku86 and Ku86 variant in the nucleus, cytosol and membrane of MM cells before and after CD40 stimulation. Unexpectedly, there were little differences observed in each of the cellular fractions for the full-length Ku86 protein levels in MM cells. Contrary to previously published data that shows increased Ku86 truncation variant in the nuclear fraction of human PBMC , we found equal levels of the Ku86v in the membrane, nuclear and cytosolic fractions in unstimulated MM cells. Yet, when the cells were stimulated with sCD40L, we did observe an increased amount of Ku86 variant in the cytosol accompanied by an increase in the DNA binding activity of Ku86v in the cytoplasm and not in the nucleus. These findings may be due to the cell type or to the fact that there appears to be little to no in vitro generated protease cleavage of Ku86 occurring during our biochemical preparations. However, the nature of the truncation is still unknown and unlikely due to post-transcriptional modification or carbohydrate modification. We are currently using more sensitive techniques of isolating various cellular fraction, performing 2-dimensional gel electrophoresis, and mass spectrometry, as well as Edmund degradation to try and determine the exact nature of this MM-specific Ku86 truncation variant. We are also currently performing studies to determine the biological function of the variant and how it might interact or disrupt the normal Ku86/Ku70/DNA-PKcs holoenzyme. Finally, we routinely see both the full-length and the truncation variant in all of our cell fractions and have not seen a time-dependent reduction in the amount of full-length Ku86 nor an increase in the variant Ku86 under any conditions. We therefore believe that the variant seen in MM cell lines is regulated in a distinct fashion from the Ku86 truncation variant that is seen in PBMCs.
Class switch recombination
DNA-dependent Protein Kinase catalytic subunit
DNA Double Stranded Break Repair
- Endo H:
Non Homologous End Joining.
This work was supported by research grants from the National Medical Research Council (NMRC), Singapore (grant #s NMRC/0489/2000 and NMRC/0734/2003); SingHealth (SU106/2004); the Department of Clinical Research, SGH; and the Singapore Cancer Syndicate (grant # SCS TS0026).
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