To the Editor:
Chronic lymphocytic leukemia (CLL) has focused a strong research effort over the last
years due to its high incidence, that will likely increase due to the progressive
ageing of the population, and the lack of truly curative therapies. Genome-wide screenings
in CLL patients revealed a group of mutations in genes covering divergent cellular
pathways [1]. Unfortunately, the mutations found did not affect to more than 13% of
the patients at its best. New genome-wide studies widen the search of mutations to
cover untranslated and regulatory regions of the genome [2].
At the sight of all of these absolutely necessary but enormously dispersed genomic
and gene expression data, some researchers have started to point to post-translational
mechanisms as the unifying defect explaining the common cellular characteristics of
CLL. Noteworthy, several preclinical studies have tested the use of inhibitors of
some of these post-translational modifications. This is the case of MLN4924-pevonedistat,
an investigational inhibitor of protein NEDDylation that is being tested in clinical
trials for the treatment of different neoplasias (https://clinicaltrials.gov/ct2/results?term=MLN4924&Search=Search).
We wanted to investigate the real extension of the NEDDylation-related alterations
in B-CLL cells. Our hypothesis is that a transversal process like this post-translational
modification may be able to provide a unifying explanation to the wide array of alterations
related to the development of CLL, thus providing molecular support to the use of
NEDDylation inhibitors in the treatment of this disease.
Current whole-cell profiling techniques do not allow the specific identification of
NEDDylated proteins, so we used a method of immunoaffinity enrichment of proteins
containing a K-GG remnant left by ubiquitin or ubiquitin-like (UBL) peptides after
digestion with trypsin. The peptides thus purified were then identified by mass spectrometry.
The application of this method over samples of B-CLL cells and CD19+ cells obtained
from healthy donors allowed us to have a wide view of the differentially ubiquitin
or UBL-modified proteins in this pathology. However, the diGly remnant left on ubiquitinated
peptides after tryptic digestion is shared by ubiquitin, NEDD8 and ISG15 modifications.
In order to discriminate those peptides originally conjugated to NEDD8 from those
modified by ubiquitination or other UBLs, we analyzed the same B-CLL samples but treated
with the NEDDylation inhibitor MLN4924.
The procedure identified a total of 3384 differentially modified peptides in CLL corresponding
to 1746 proteins. 651 site modifications were unreported at the date of the screening.
Of those K-GG remnant modifications, 2142 (63%) corresponded to a ≥2.5-fold increase
in B-CLL cells with respect to the healthy controls, while only 401 (12%) were reduced
≥2.5-fold. Of those 2142 augmented modifications, 353 were notably reverted by the
incubation with MLN4924 (threshold 2.5-fold) (Fig. 1). Noteworthy, 76% of these sites
were not detected by the UbiSite antibody in the work by Akimov et al. [3].
Fig. 1
List of the 353 over-modified and MLN4924-sensitive lysines found in CLL B cells.
On the left, the heatmap shows the fold change in the modification state of the lysines
in CLL B cells compared to healthy donor cells at basal state and after treatment
with 0.25 µM MLN4924. The sites are sorted by their sensitivity to MLN4924, expressed
as the difference in the fold change between the basal and MLN4924 conditions.
Overall, MLN4924 affected the amount of the K-GG remnant in 1666 sites of 1008 proteins
(threshold 2.5-fold); post-translational modifications induced by MLN4924 were found
in 609 proteins, while modifications impaired by the inhibitor were found in 399 proteins.
Interestingly, 37 proteins displayed modifications of both types.
Although these data suggest an increment of NEDDylated proteins in CLL, we found no
differences in the NEDD8 present in the serum of a group of patients when compared
to that of healthy donors (Supplementary figure 1). However, the expression of the
genes coding for the E1 (NAE1) and the two E2’s (UBE3F and UBE2M) specific of the
NEDDylation pathway were higher in peripheral mononuclear cells from the patients
(Supplemental Fig. 2).
Our screening showed that the modification status of several members of the NEDDylation
cascade were increased in CLL and sensitive to the action of the NEDDylation inhibitor
(Supplementary Table 1). It also unveiled the altered post-translational modification
of a group of proteins related to the ubiquitination machinery, many of them sensitive
to the action of MLN4924 (Supplementary Table 2). We found alterations in the post-translational
modification of many proteins involved in pathways previously described as relevant
to the pathogenesis of CLL (Supplementary Tables 3–7). These pathways include DNA
repair, RNA processing, and the NF-kB pathways, previously reported to be modulated
by post-translational modifications, although our screening unveiled novel proteins
and lysine targets, as well as a their sensitivity to MLN4924 treatment. This is the
case of the NF-kB pathway where, surprisingly, no change in IkB modification was detected
in our screening [4, 5]. Rather, upstream regulatory members of the pathway showed
these kind of changes (see Supplementary Table 7). Among them, TANK stood out for
the over-modification of three of its lysines in CLL, that could be partially reverted
by MLN4924.
Structural proteins associated with phenotypical changes in CLL cells also were aberrantly
modified. This is the case of proteins of the chromatin and the cytoskeleton (Supplementary
Tables 4 and 5). Vimentin levels in CLL B cells have been inversely associated with
the apparition of smudge cell in peripheral blood smear preparations [6, 7] and with
a worse prognosis [8]. Our screening unveiled an increase in post-translational modifications
of vimentin and other cytosqueleton proteins and treatment with MLN4924 reverted those
modifications along with a reduction in the amount of smudge cells (Supplemental Fig. 3).
Although a more profound study is needed, these results suggest a negative effect
of NEDDylation over the function of vimentin, and a role of post-translational modifications
in the molecular basis of a characteristic cellular manifestation of CLL.
Post-translational modifications of p53 play a key role in its function as tumor supressor
and many of them have been described [9, 10]. Our screening did not detect modifications
in the C-terminal lysines 370, 372, and 373 of p53 in CLL. By contrast, we found a
strong modification of lysine 120, that was sensitive to the treatment with MLN4924
(Supplementary Table 8). Ubiquitination and acetylation of this lysine have been previously
described [11, 12]. To test whether this residue of p53 could also be NEDDylated,
we generated the mutant K120R and cotransfected it in cells along with MDM2 and NEDD8.
Compared to wild-type p53, this mutant showed a reduced sensitivity to NUB1L, a protein
that specifically targets NEDDylated proteins to the proteasome [13], suggesting a
reduction in its NEDDylation level (Supplementary Fig. 4).
We then investigated the role of NEDDylation of lysine 120 on the function of p53.
To this end, we used the LLC cell line MEC1 that is defective in p53. Transfection
of wild-type p53 in MEC1 cells induced a reduction in viability that was partially
reverted by cotransfection with MDM2 and NEDD8. K120R mutant also induced a reduction
in MEC1 cells viability, although NEDD8 cotransfection did not revert it (Fig. 2A).
These experiments suggest that p53 NEDDylation in lysine 120 reduces its capacity
to act as a tumor suppressor.
Fig. 2
Molecular study of the effect of K120 NEDDylation over p53 function as tumor suppressor.
A NEDDylation of p53 at lysine 120 affects its transactivation potential and the cell
viability. XTT cell viability assay of MEC1 cells nucleofected with p53 wt or p53
K120R in the presence or absence of MDM2 and NEDD8. The effect of fludarabine in MEC1
viability in each condition is also depicted. B The luciferase reporter vector pG13Luc
was used to measure the transactivation potential of p53 wt or the K120R mutant in
the presence or absence of NEDD8. C NEDD8 interferes with the acetylation of p53 at
lysine 120. Luciferase assay of pG13Luc cotransfected with p53 wt or the K120R mutant
along with MDM2, the acetylase TIP60 and increasing amounts of NEDD8. D Analysis by
RT-qPCR or the expression of four p53 target genes in HEK293T cells transfected with
expression plasmids for the indicated proteins. E Western blot analysis of the acetylation
of p53 at lysine 120 in HEK293T cells transfected with expression plasmids for the
indicated proteins. F NEDDylation impairs p53 interaction with Bcl-2. Coimmunoprecipitation
of FLAG-tagged p53 wt or K120R mutant with Bcl-2 in the presence of increasing amounts
of NEDD8. Whole-cell extracts of p53 wt- or K120R mutant-transfected HEK293T cells
were precipitated with an anti-FLAG antibody and the associated Bcl-2 was revealed
by western blot.
We next investigated the molecular basis of this impairment of p53 function. First,
we tested the effect of lysine 120 NEDDylation on the transactivation potential of
p53. In our transient transfection experiments, K120R mutation did not significantly
affect p53 transactivation capacity but rather incremented it. However, when NEDDylation
was induced by MDM2 and NEDD8 overexpression, p53 experimented a strong reduction
in its transactivation potential while for p53K120R the inhibition was milder (Fig. 2B).
Acetylation of lysine 120 has been demonstrated to be essential for p53 to develop
its full transactivation potential. Indeed, cotransfection of TIP60, one of the acetylases
known to modify lysine 120 of p53, induced an increase in the activation of a p53
reporter construct (Fig. 2C), as well as in the expression of p53 target genes (Fig. 2D).
We then wanted to study whether NEDDylation could be interfering with lysine 120 acetylation.
Cotransfection of MDM2 and NEDD8 impaired TIP60 enhancement of p53 transactivation
potential strongly when lysine 120 was intact (Fig. 2C, D). A western blot analysis
with an antibody specific for K120-acetylated p53 demonstrated that NEDDylation reduced
the acetylation of lysine 120 (Fig. 2E).
Forced ubiquitination of both p53 forms induced a similar reduction in their transactivation
capacity (Supplementary Fig. 5A). However, this reduction in p53 transactivation activity
was due to a destabilization of the protein that does not occur with its NEDDylation
(Supplementary Fig. 5B).
Acetylation of lysine 120 has also been related to the transcriptional-independent
induction of apoptosis by p53, through the modulation of its interaction with Bcl-2
[14, 15]. When overexpressed in HEK293 cells, p53 interacted with Bcl-2, as we could
demonstrate in coimmunoprecipitation experiments. However, the amount of Bcl-2 pulled
down by p53 was reduced in a dose dependent manner when MDM2 and NEDD8 were transfected
along (Fig. 2F). Accordingly, K120R mutation of p53 greatly impaired its interaction
with Bcl-2.
This work provides an overall view of the UBL modifications in chronic lymphocytic
leukemia, that brings the idea that an alteration in such transversal processes could
be an underlying link among the variety of pathways involved in this pathology, giving
rationale for the use of MLN4924 in its treatment.
Supplementary information
Supplemental figures
Supplemental tables