Mutations in the PCNA-binding site of CDKN1C inhibit cell proliferation by impairing the entry into S phase
© Borges et al.; licensee BioMed Central. 2015
Received: 29 November 2014
Accepted: 16 March 2015
Published: 28 March 2015
CDKN1C (also known as P57 kip2 ) is a cyclin-dependent kinase inhibitor that functions as a negative regulator of cell proliferation through G1 phase cell cycle arrest. Recently, our group described gain-of-function mutations in the PCNA-binding site of CDKN1C that result in an undergrowth syndrome called IMAGe Syndrome (Intrauterine Growth Restriction, Metaphyseal dysplasia, Adrenal hypoplasia, and Genital anomalies), with life-threatening consequences. Loss-of-function mutations in CDKN1C have been identified in 5-10% of individuals with Beckwith-Wiedemann syndrome (BWS), an overgrowth disorder with features that are the opposite of IMAGe syndrome. Here, we investigate the effects of IMAGe-associated mutations on protein stability, cell cycle progression and cell proliferation. Mutations in the PCNA-binding site of CDKN1C significantly increase CDKN1C protein stability and prevent cell cycle progression into the S phase. Overexpression of either wild-type or BWS-mutant CDKN1C inhibited cell proliferation. However, the IMAGe-mutant CDKN1C protein decreased cell growth significantly more than both the wild-type or BWS protein. These findings bring new insights into the molecular events underlying IMAGe syndrome.
KeywordsCell cycle CDK-inhibitor IMAGe syndrome Cyclin Beckwith Wiedemann syndrome Intrauterine growth restriction
CDKN1C (also known as p57kip2) is a cyclin-dependent kinase inhibitor sharing CDKN1B (p27Kip1) and CDKN1A (p21WAF1/Cip1) homology that has a key role in inhibiting cell cycle progression by blocking the cells in G1 phase . It is located on chromosome 11p15.5 and is part of a cluster of imprinted genes. The CDKN1C protein has 316 amino acids (AA) and consists of three structurally distinct domains: the N-terminal domain (AA 1 – 110), necessary for CDK inhibition; a central proline-alanine series of repeats (PAPA-repeats, AA 156 – 213), and a highly conserved C-terminal region (QT domain, AA 214 – 316), where the PCNA binding site is located [2,3]. In nearly all tissues, CDKN1C is expressed from the maternal allele while the paternal allele is silenced [1,2].
Recently, our group identified missense mutations in the PCNA-binding domain of CDKN1C in families with IMAGe syndrome (MIM# 614732), characterized by Intrauterine growth retardation, Metaphyseal dysplasia, Adrenal hypoplasia and Genital anomalies. Interestingly, CDKN1C mutations have previously been identified in Beckwith-Wiedemann Syndrome (BWS; MIM# 130650) and are distributed throughout entire length of the coding sequence of the gene. These BWS-associated mutations are either missense mutations that disrupt the cyclin-dependent kinase binding domain, or nonsense mutations, both of which result in protein loss-of-function [3,4]. CDKN1C mutations have been found in 5–10% of sporadic BWS cases and in approximately 40% of cases with a family history .
We hypothesize that IMAGe syndrome mutations result in loss of PCNA-binding and a gain-of-function of CDKN1C. Previous studies demonstrated that IMAGe-mutant CDKN1C and BWS-mutant CDKN1C have differential effects on cell cycle progression, developmental processes, suggesting that domain-specific mutations act through distinct mechanisms . Early studies have also shown that targeted eye expression of IMAGe-mutant CDKN1C mutations in Drosophila cause severe growth defects compared to wild type CDKN1C. Furthermore, an in vitro assay showed that IMAGe-mutant CDKN1C protein presents alteration in its ubiquitination pattern . Here, we aim to investigate the molecular mechanisms underlying the IMAGe mutations. To address this, we performed functional studies with wild-type, IMAGe-mutant and BWS-mutant CDKN1C proteins. IMAGe-mutant protein consists of a mutation in the PCNA binding domain and an intact cyclin-dependent kinase binding domain whereas CDKN1C BWS-mutant protein contains a mutation in the cyclin-dependent kinase binding domain and a wild-type PCNA binding site. Our results showed that missense mutations in the PCNA-binding site of CDKN1C lead to protein stabilization, impaired entry into S-phase, culminating in decreased cell proliferation. Moreover, IMAGe-mutants displayed different effects relative to BWS-mutants, suggesting that domain-specific mutations have differential effects on cell-cycle progression and cell proliferation.
Loss of PCNA binding in IMAGe-mutant CDKN1C results in increased protein stability and loss of normal oscillation of CDKN1C protein during cell cycle progression
Western blot analysis showed that in cells transfected with either the wild-type or BWS-mutant CDKN1C, the CDKN1C protein levels oscillated, peaking at 3 and 15 hours after the release. On the other hand, protein levels of IMAGe-mutant CDKN1C remained at constant levels throughout the entire 24-hour time course (Figure 2B). These results show that IMAGe mutations result in increased stability and a loss of normal oscillation of CDKN1C protein levels. This is consistent with previous results showing loss of ubiquitination  and indicates that normal progression through the cell cycle is disturbed when the IMAGe-mutant is expressed.
IMAGe-mutant CDKN1C impairs entry into S phase in synchronized cells
In order to understand the effects of CDKN1C on cell cycle progression, we examined cell cycle phase distribution of the cells from the experiment described in Figure 2A. Upon release at G1/S phase, cells transfected with empty plasmid or BWS-mutant CDKN1C progressed synchronously through the entire cell cycle (Figure 2C) whereas a larger proportion of wild-type and IMAGe-mutant CDKN1C transfected cells were unable to progress through the cell cycle and remained in G1 phase after T0 (Figure 2C). These data indicate that IMAGe-mutant CDKN1C protein prevents G1/S phase transition as CDKN1C wild-type protein.
Given the differences observed between wild-type, IMAGe-mutant and BWS-mutant CDKN1C in the G1 and S-phase cell distributions, we also examined levels of cell cycle regulatory protein cyclin-A, a well established S-phase marker . Protein lysates from cells transfected with IMAGe-mutant CDKN1C did not exhibit accumulation of cyclin A as observed in cells transfected with empty vector, wild-type, and BWS-mutant CDKN1C (Figure 3B). This data shows that the loss of S-phase transition occurs in cells transfected with IMAGe-mutant CDKN1C, but not in empty vector, wild-type, or BWS-mutant CDKN1C transfected cells. In accordance with our results, Brioude et al.,  found a higher percentage of cells in G1 phase in asynchronous cells transfected with IMAGe-mutant. Collectively, these findings show that the increased CDKN1C stability conferred by mutations in the PCNA-binding domain mutations leads to impaired entry into S phase.
IMAGe-mutant CDKN1C decreases cell proliferation
To investigate the effects of CDKN1C protein stability on cell proliferation we performed a clonogenic assay with the wild-type, BWS-mutant and IMAGe-mutant CDKN1C in HEK293T and SW13 cell lines. After transfection cell suspensions were split into six-well plates. The cell cultures were incubated for 7 days and the colonies were then rinsed with PBS, fixed with methanol, and stained with Crystal violet stain. Colonies with more than 50 cells were counted. Assays were performed in triplicate.
CDKN1C is a negative regulator of cell proliferation and the effects observed on the wild-type transfected cells may be attributed to a combination of the CDK-inhibitory and PCNA domains of the CDKN1C. Moreover, the remaining effects demonstrated by BWS-mutants probably are associated with the intact PCNA-binding domain of CDKN1C, as described previously . In the IMAGe-mutant transfected cells, the progression through the cell cycle is impaired as cyclical degradation of CDKN1C is lost. The G1-phase cell-cycle inhibition is increased due to increased stability of CDKN1C IMAGe mutants, which maintains an intact cyclin-dependent kinase binding domain, resulting in decreased proliferation and the undergrowth phenotype observed in patients with IMAGe syndrome. Previous reports have described the in vitro effects of variations in CDKN1C levels on cell growth [10,11]. In vivo models have showed that mouse embryonic growth is sensitive to the precise dosage of Cdkn1c and excess of this protein results in dose dependent embryonic growth retardation , a phenotype seen in patients with IMAGe Syndrome.
Further expansion of the phenotypes associated with mutations in CDKN1C’s PCNA binding domain suggests phenotypic heterogeneity. Recently, mutations inducing different missense changes of the arginine at amino acid 279 were found in individuals with IMAGe Syndrome and Silver Russell Syndrome (SRS, MIM #180860), characterized by prenatal and postnatal growth retardation and dysmorphic features. We hypothesize that these differences in amino acid changes (arginine to leucine in SRS versus Arginine to Proline in IMAGe Syndrome) are associated with a both differential loss of binding to PCNA and the effects of modifier genes . In addition to SRS, missense mutations located in the highly conserved PCNA binding domain have also been associated with heterogeneous clinical phenotypes with growth restriction and variable to no adrenal failure or skeletal abnormalities and onset of diabetes in early adulthood [13,14]. There the phenotypic spectrum associated with missense mutations in the CDKN1C PCNA binding domain suggests the importance of genetic modifiers in disease manifestation.
Our data suggests that mutations in the PCNA-binding domain of CDKN1C leads to increased protein stability, a block in the G1 phase and impaired S-phase entry, and decreased cell proliferation. Our findings demonstrate that domain-specific mutations affect different aspects of cell-cycle progression and cell proliferation, which give rise to the two opposing phenotypes: BWS and IMAGe syndrome. The data presented here give the further direct evidence of how the PCNA-binding site mutations in CDKN1C affect the cell cycle and cause IMAGe syndrome.
Intrauterine growth restriction, methaphyseal dysplasia, adrenal hypoplasia congenital and genital anomalies
Cyclin-dependent kinase inhibitor 1C
Cyclin dependent kinase, BWS, Beckwith Wiedemann syndrome
This work was supported by NIH grants HD044513 to EV and F31HD068136 and UCLA Institutional funds to VAA and fellowship from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP process number 2012/09391-0) to KSB.
- Matsuoka S, Edwards MC, Bai C, Parker S, Zhang P, Baldini A, et al. p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. Genes Dev. 1995;9:650–62.View ArticlePubMedGoogle Scholar
- Matsuoka S, Thompson JS, Edwards MC, Bartletta JM, Grundy P, Kalikin LM, et al. Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15. Proc Natl Acad Sci U S A. 1996;93:3026–30.View ArticlePubMed CentralPubMedGoogle Scholar
- Romanelli V, Belinchón A, Benito-Sanz S, Martínez-Glez V, Gracia-Bouthelier R, Heath KE, et al. CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms. Am J Med Genet A. 2010;152A:1390–7.PubMedGoogle Scholar
- Arboleda VA, Lee H, Parnaik R, Fleming A, Banerjee A, Ferraz-de-Souza B, et al. Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome. Nat Genet. 2012;44:788–92.View ArticlePubMed CentralPubMedGoogle Scholar
- Nishitani H, Shiomi Y, Iida H, Michishita M, Takami T, Tsurimoto T. CDK inhibitor p21 is degraded by a proliferating cell nuclear antigen-coupled Cul4-DDB1Cdt2 pathway during S phase and after UV irradiation. J Biol Chem. 2008;283:29045–52.View ArticlePubMed CentralPubMedGoogle Scholar
- Brioude F, Oliver-Petit I, Blaise A, Praz F, Rossignol S, Jule ML, et al. CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome. J Med Genet. 2013;50:823–30.View ArticlePubMedGoogle Scholar
- Hamajima N, Johmura Y, Suzuki S, Nakanishi M, Saitoh S. Increased protein stability of CDKN1C causes a gain-of-function phenotype in patients with IMAGe syndrome. PLoS One. 2013;8:e75137.View ArticlePubMed CentralPubMedGoogle Scholar
- Girard F, Strausfeld U, Fernandez A, Lamb NJ. Cyclin A is required for the onset of DNA replication in mammalian fibroblasts. Cell. 1991;67:1169–79.View ArticlePubMedGoogle Scholar
- Watanabe H, Pan ZQ, Schreiber-Agus N, DePinho RA, Hurwitz J, Xiong Y. Suppression of cell transformation by the cyclin-dependent kinase inhibitor p57KIP2 requires binding to proliferating cell nuclear antigen. Proc Natl Acad Sci U S A. 1998;95:1392–7.View ArticlePubMed CentralPubMedGoogle Scholar
- Chen B, Zhao R, Su CH, Linan M, Tseng C, Phan L, et al. CDK inhibitor p57 (Kip2) is negatively regulated by COP9 signalosome subunit 6. Cell Cycle. 2012;11:4633–41.View ArticlePubMed CentralPubMedGoogle Scholar
- Zhao R, Yang HY, Shin J, Phan L, Fang L, Che TF, et al. CDK inhibitor p57 (Kip2) is downregulated by Akt during HER2-mediated tumorigenicity. Cell Cycle. 2013;12:935–43.View ArticlePubMed CentralPubMedGoogle Scholar
- Andrews SC, Wood MD, Tunster SJ, Barton SC, Surani MA, John RM. Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. BMC Dev Biol. 2007;21(7):53.View ArticleGoogle Scholar
- Kato F, Hamajima T, Hasegawa T, Amano N, Horikawa R, Nishimura G, et al. IMAGe syndrome: clinical and genetic implications based on investigations in three Japanese patients. Clin Endocrinol. 2014;80:706–13.View ArticleGoogle Scholar
- Kerns SL, Guevara-Aguirre J, Andrew S, Geng J, Guevara C, Guevara-Aguirre M, et al. A novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes. J Clin Endocrinol Metab. 2014;99:2117–22.View ArticleGoogle Scholar
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.