- Research Article
- Open Access
Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development
- Jianjun Liu1Email author,
- Kartiki Vasant Desai2,
- Yuqing Li1,
- Shakeela Banu2,
- Yew Kok Lee2,
- Dianbo Qu1,
- Tuomas Heikkinen3,
- Kirsimari Aaltonen3, 4,
- Taru A. Muranen3,
- Tasneem Shabbir Kajiji1,
- Carine Bonnard1,
- Kristiina Aittomäki5,
- Karl von Smitten6,
- Carl Blomqvist4, 8,
- John L. Hopper9,
- Melissa C. Southey9,
- Hiltrud Brauch10,
- The GENICA Consortium,
- Georgia Chenevix-Trench11,
- Jonathan Beesley11,
- Amanda B. Spurdle11,
- Xiaoqing Chen11,
- Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer12,
- Australian Ovarian Cancer Study Group11, 12,
- Kamila Czene7,
- Per Hall7,
- Heli Nevanlinna3 and
- Edison T. Liu2Email author
© Springer Science+Business Media B.V. 2010
- Received: 2 December 2009
- Accepted: 16 March 2010
- Published: 13 April 2010
Multiple lines of evidence suggest regulatory variation to play an important role in phenotypic evolution and disease development, but few regulatory polymorphisms have been characterized genetically and molecularly. Recent technological advances have made it possible to identify bona fide regulatory sequences experimentally on a genome-wide scale and opened the window for the biological interrogation of germ-line polymorphisms within these sequences. In this study, through a forward genetic analysis of bona fide p53 binding sites identified by a genome-wide chromatin immunoprecipitation and sequence analysis, we discovered a SNP (rs1860746) within the motif sequence of a p53 binding site where p53 can function as a regulator of transcription. We found that the minor allele (T) binds p53 poorly and has low transcriptional regulation activity as compared to the major allele (G). Significantly, the homozygosity of the minor allele was found to be associated with an increased risk of ER negative breast cancer (OR = 1.47, P = 0.038) from the analysis of five independent breast cancer samples of European origin consisting of 6,127 breast cancer patients and 5,197 controls. rs1860746 resides in the third intron of the PRKAG2 gene that encodes the γ subunit of the AMPK protein, a major sensor of metabolic stress and a modulator of p53 action. However, this gene does not appear to be regulated by p53 in lymphoblastoid cell lines nor in a cancer cell line. These results suggest that either the rs1860746 locus regulates another gene through distant interactions, or that this locus is in linkage disequilibrium with a second causal mutation. This study shows the feasibility of using genomic scale molecular data to uncover disease associated SNPs, but underscores the complexity of determining the function of regulatory variants in human populations.
- p53 binding sites
- PRKAG2 gene
- ER negative tumors
- Breast cancer susceptibility
There is a great interest in the role of regulatory variation in phenotypic evaluation and disease development. Early evolutionary biologists suggested that genetic variation within regulatory sequences is the main driving force behind phenotypic evolution (Wray 2007). Based largely on the observation that coding sequences usually show limited divergence between closely related species such as human and chimpanzees (King and Wilson 1975), it was argued that such moderate divergence of coding sequences cannot account for the profound phenotypic difference between species and it was proposed that regulatory mutations within non-coding sequences (regulatory variation) constitutes the main genetic basis of phenotypic evolution. This interest on regulatory variation is also motivated by the discovery of several regulatory variants that underline complex disease traits (Knight 2005) and further augmented by the recent findings that gene expression shows substantial variation in human and many model organisms, and that such expression variation is, at least partially, due to germ-line genetic variation (Sladek and Hudson 2006).
Despite this great interest, only few regulatory polymorphisms have been characterized molecularly and linked to disease development. For example, a T/G polymorphism within the intronic promoter of MDM2, a strong negative regulator of p53 protein activity, was shown to influence the binding affinity of transcription activator Sp1 and thus the expression level of MDM2, which in turn resulted in decreased levels of p53 protein, leading to accelerated tumor formation (Bond et al. 2004). Recently, the meta-analysis of all the 21 subsequent association studies of the polymorphism showed a convincing association of the homozygous genotype of the minor allele with an increased risk for cancer development, especially in lung cancer and smoking-related cancers (Hu et al. 2007). The limited progress made on identifying disease-related regulatory variants is largely due to a difficulty in delineating regulatory sequences and thus their germ-line polymorphisms. The identification of regulatory sequences has been pursued by using a comparative genomics approach where the conservation analysis of non-coding sequences between closely related species is used as a primary tool for inferring regulatory sequences. Such an approach is prone to high false discoveries and is confounded by the fact that many functional transcription factor binding sites reside on species specific repetitive sequences (Bourque et al. 2008). Using eQTL strategies, recent efforts attempted to map regulatory variation to particular genomic regions (Pastinen and Hudson 2004), but the extensive linkage disequilibrium in human and model organism genomes limits the mapping resolution of such genetical genomic analyses. Recent advances on technologies like chromatin immunoprecipitation (ChIP) followed by hybridization to an array chip (ChIP-Chip) (Cawley et al. 2004) or by shotgun sequencing of ChIP pull-down DNA fragments (ChIP-seq or ChIP-PET) (Cawley et al. 2004; Wei et al. 2006) have made it possible to identify bona fide regulatory sequences on a genome-wide scale. These binding sites can then be subjected to functional interrogation of germ-line polymorphisms within the binding sequences.
In this study, we performed a forward genetic study of a group of the p53 binding sites that were identified through a genome-wide ChIP-PET analysis (Wei et al. 2006). By the identification of known single nucleotide polymorphisms (SNPs) within p53 binding motif sequences and subsequently the molecular and genetic characterization of such polymorphisms, we found a common SNP within an intronic p53 binding motif that could influence p53 protein binding, transcription regulation and breast cancer development.
Summary of the samples from the five breast cancer studies of European population
The SASBAC study consisted of 1,596 breast cancer patients that were randomly selected from a population-based Swedish cohort that included all Swedish-born breast cancer patients between 50 and 74 years of age and resident in Sweden between October 1993 and March 1995. A total of 1,730 age-matched controls were randomly selected from the Swedish Registry of Total Population. A total of 1,290 cases and 1,483 controls of the SASBAC study provided DNA and were successfully genotyped in the current study. Finnish breast cancer cases consisted of two series of unselected breast cancer patients and additional familial cases ascertained at the Helsinki University Central Hospital. The first series of 884 patients was collected in 1997–1998 and 2000 and covers 79% of all consecutive, newly diagnosed cases during the collection periods. And the second series, containing 986 consecutive newly diagnosed patients, was collected in 2001–2004 and covers 87% of all such patients treated at the hospital during the collection period. An additional 538 familial breast cancer cases were collected at the same hospital. A total of 1,287 anonymous, healthy female population controls were collected from the same geographical regions in Southern Finland as the cases. A total of 2,222 cases and 1,256 controls of the HEBCS study were successfully genotyped in the current study. The ABCFS study is a population based case–control-family study. Briefly, 1,610 cases were composed of three age-groups of patients from two metropolitan areas selected in 1992–1999 in Melbourne and 1993–1998 in Sydney, Australia. A total of 1,077 controls were identified from the electoral rolls from the same geography areas with 5-year age frequency matched. A total of 1,117 cases and 601 controls of the ABCFS study provided DNA and were successfully genotyped in the current study. The GENICA study consisted of 1,021 incident breast cancer cases and 1,015 age matched controls enrolled between 2000 and 2004 from the Greater Bonn area, Germany. The controls were randomly selected from population registries for 31 communities in the greater Bonn area who matched to cases in 5-year age classes. Both cases and controls were of Caucasian ethnicity and below 80 years of age. A total of 1,015 cases and 1,002 controls of the GENICA study were successfully genotyped in the current study. The sample of the kConFab study consisted of 640 cases from multiple-case breast and breast-ovarian families recruited though family cancer clinics across Australia and New Zealand from 1998 to the present. A total of 1,009 controls were ascertained by the Australian Ovarian Cancer Study identified from the electoral rolls from all over Australia from 2002 to 2006. From these studies, 483 patients with no family history of mutations in BRCA1 and BRCA2, or who were the index for the family, and the youngest breast cancer affected family member, and 855 controls provided DNA and were successfully genotyped in the current study. All the samples of the five studies were used in several previous genetic association studies (Easton et al. 2007; Ahmed et al. 2009; Dunning et al. 2009). In total, 6,127 breast cancer cases and 5,197 controls were analyzed in the current study.
All the samples were recruited with informed consent, and this study was approved by local Institutional Review Boards.
Genotyping analysis of SNPs was performed by using the MALDI-TOF mass spectrometry-based MassARRAY™ system from the Sequenom (San Diego, CA, US) (the samples of SASBAC, ABCFS, GENICA, and KONFAB) as well as the TaqMan assays from the AppliedBiosystesm (ABI) (Foster City, CA, US) (HSBCA). All genotyping plates included positive and negative controls, DNA samples were randomly assigned to the plates, and all genotyping results were generated and checked by laboratory staff unaware of case–control status. The genotype frequency was in Hardy–Weinberg equilibrium in each of the five samples.
Lymphoblatoid cell lines and culture
Lymphoblastoid cell lines (LCLs) used in this study were obtained from the Coriell depository (http://www.coriell.org/). Cells were cultured in RPMI medium supplemented with 20% fetal bovine serum. For ChIP, real-time qPCR and western blot analyses, cells were treated with 5FU at the concentration of 375 µM for various numbers of hours. All the drug treatments were done during the log phase of cell growth (about 1–1.5 millions of cells per ml). Cells were harvested after culture with or without drug treatment(s) and stored at −80 degrees. 5FU was obtained from the Sigma.
ChIP assays were performed in LCLs using the protocol described previously (Weinmann and Farnham 2002; Wells and Farnham 2002). The DO1 monoclonal antibody for p53 (Santa Crux Biotechnology, Santa Cruz, CA) was used for immunoprecipitation, and real-time quantitative PCR analyses were performed in triplicate using the PRISM 7,900 Sequence Detection System and the SYBR protocol as described (Wei et al. 2006). The real-time PCR analysis was performed using the following primers: CCATCCTGCCTGAGCATGTCTGAAC (forward) and CCGGCTTTGCCAGACAATTGG (reverse) (For PRKAG2); CAGGCTGTGGCTCTGATTGGCTTTC (forward) and GCTGGCAGATCACATACCCTGTTCAGAGTA (reverse) (For CDKN1A); ACCCACACTGTGCCCATCTACGAG (forward) and TCTCCTTAATGTCACGCACGATTTCC (reverse) (For Actin). Relative occupancy was calculated by determining the immunoprecipitation efficiency (ratios of the amount of immunoprecipitated DNA over that of the input sample) and normalized to the level observed at a control region, which was defined as 1.0. The control region was a distal site around the binding site for Actin and not enriched by the immunoprecipitation.
Allele enrichment analysis of ChIP pull-down DNAs by real-time PCR
The allele enrichment analysis of the ChIP input and pull-down DNAs from heterozygous cell lines was performed in triplicate by real-time quantitative PCR using a made-to-order TaqMan SNP assay for rs1804674 from the ABI. The quality of the TaqMan SNP assay was first verified by genotyping 30 CEPH DNA samples, and all the genotype results are consistent with the ones from the HAPMAP project (data not shown). For real-time PCR analysis, the Ct value difference (∆Ct) between G and T alleles of a ChIP pull-down DNA was normalized by the ∆Ct value of the corresponding input DNA (reflecting the equal numbers of G and T alleles in normal genomic DNAs from the heterozygous cell lines). The normalized ∆Ct value (∆∆Ct) was then used to calculate the enrichments (Fold Change using the formula of 2∆∆Ct) of the wild-type G allele over the mutant T allele in the ChIP pull-down DNA.
Expression analysis by real-time PCR
We studied the induction of p53 in LCLs using 50, 100, 150, and 375 μM 5FU. We achieved maximal response at 100 μM 5FU with minimal cell death over 48 h of treatment (data not shown). To determine gene expressions changes, cells were plated at 0.3 million cells per ml and treated with 100 µM 5FU or DMSO (vehicle) for 4, 8, and 24 h. For each time point, cells were harvested and total RNA was extracted using QIAGEN RNeasy Kit. The SuperScript III First-Strand Synthesis System (Invitrogen, CA, USA) was used to reverse transcribe 2 µg of total RNA to 20 µl cDNA. cDNA was diluted to 80 and 2 µl was used as template for real-time PCR.
Real-time PCR analysis was done in the ABI Prism 7700 sequence detection system using SYBR Green from ABI. Primers were designed using the online Primer 3 program. Primer sequences are as follows: PRKAG2: CCCTATCAGTGGGAATGCAC (forward), GCTCATCCAGGTTCTGCTTC (reverse); CDKN1A: TTAGCAGCGGAACAAGGAGT (forward), CAACTACTCCCAGCCCCATA (reverse); Beta-ACTIN: TCCCTGGAGAAGAGCTACGA (forward), AGGAAGGAAGGCTGGAAGAG (reverse). Ct values obtained for PRKAG2 and CDKN1A were normalized to Beta-ACTIN Ct values. The normalized Ct (ΔCt) values were then used to calculate the difference (ΔΔCt) between 5FU and DMSO treated samples for each timepoint. Fold change of PRKAG2 and CDKN1A at each timepoint was then calculated as 2−ΔΔCt.
Primers for PRKAG2 isoforms
Since we did not observe change in PRKAG2 expression using primers that detect all isoforms, we hypothesized that p53 may differentially regulate them. Primers were designed using the online NCBI Primer-BLAST program, ensuring specificity of primer pairs to the intended template. Primer sequences are as follows: PRKAG2 isoform ‘a’ (NM_016203.3): CGCGTGCACATTCCGGACCT (forward), GCCGAAGGGGCTGTCCACCT (reverse) PRKAG2 isoform ‘b’ (NM_024429.1): CCTCCTCCTCCCCCTCAGGC (forward), TGAGTCTTCTACTGCTTCGTCCTCG (reverse) PRKAG2 isoform ‘c’ (NM_001040633.1): CCAGGACCCCTTGGGGCTGA (forward), CCGAAGGGGCTGTCCACCTTT (reverse). However, none of these isoforms were changed following 5FU treatment (data not shown).
Promoter assay analysis
A 226 bp region encompassing the intronic p53 binding site within PRKAG2 was amplified using hotstart PCR with forward primer 5′-TAGGAGACCTGGGGGACTTT-3′ and reverse primer 5′-CAGGCATCTCGAAGAGATCA-3′ and 50 ng of genomic DNAs isolated from the individuals carrying either the wild-type (WT) G or mutant (MUT) A allele. The PCR conditions were; 94°C for 15 min, followed by 35 cycles of denaturation at 94°C for 45 s, annealing 55°C for 45 s, and extension at 72°C for 45 s. The resultant PCR products of 226 bp were purified from agarose gels and cloned using TOPO-TA cloning system (Invitrogen, Calsbad, CA). The genotypes of the cloned DNA fragments were confirmed by DNA sequencing. Subsequently, the DNA fragments were subcloned into the upstream of TATA-luciferase (fire-fly) containing pGL4 vector (Promega) using Kpn I and Xho I restriction enzymes (New England Biolabs).
Reporter assay analysis was performed by using both HCT116 wild type and null for p53 cells (provided by Dr Bert Vogelstein’s lab at the Johns Hopkins School of Medicine) that were maintained in DMEM containing 10% fetal bovine serum. 5 × 104 cells were plated in triplicate in 24-well plates and transfected next day with 250 ng of either parent TATA-luc, WT-TATA-luc or MUT-TATA-luc plasmid DNAs under serum free conditions using 1 μg per well of Lipofectamine 2000 (Invitrogen, Calsbad, CA). 2.5 ng of pRL-CMV vector containing renilla luciferase was co-transfected in each well to normalize transfection efficiency across wells. After 8 h the cells were recovered for 3 h in serum containing medium, following which the cells were treated for 12 h with 375 μM 5-Fluorouracil or DMSO. The cells were lysed in passive lysis buffer and promoter assays were carried out as per manufacturer’s instructions using Promega Dual-luciferase assay system. The values obtained for each construct were normalized as fold-change to that of the activity of parental TATA-luc vector in HCT116 WT cells (designated as 1).
Hardy–Weinberg Equilibrium (HWE) test was performed in the five control samples separately, and no evidence for deviation from HWE was found. Association analysis was performed using the χ2 test under a recessive model of inheritance. For the joint association analyses of the combined samples, the Mantel–Haenszel method for meta-analysis was used by assuming fixed effect. All statistical analyses were performed by using the StataSE8 system.
Identification of p53 binding site SNPs
Of 542 high confidence p53 binding sites identified in HCT116 cell line by our genome-wide ChIP-PET mapping analysis (Wei et al. 2006), we selected 235 sites for SNP mining where an unequivocal p53 consensus binding motif sequence (5′-RRRCWWGYYYRRRCWWGYYY-3′) can be found (see Supplementary Fig. 1 for the position weighted matrix presentation of the consensus sequence). The sequences of the 235 binding sites were blasted against the dbSNP database (version 115), and 14 SNPs were identified to be directly located within the binding motifs. Of the 14 SNPs, 12 SNPs were successfully genotyped in 76 anonymous germ-line DNA samples in Caucasian population, and six SNPs were confirmed to be polymorphic with a minor allele frequency (MAF) above 1%.
Of the six confirmed p53 binding motif germ-line polymorphisms, rs1860746 was found to be located within the consensus motif sequence of an p53 binding site in the third intron of the PRKAG2 gene where high p53 protein occupancy was observed (Wei et al. 2006). rs1860746 (a G/T substitution) is located at one of the highly conserved bases of p53 motif sequence, and its minor allele T causes a mismatch to the p53 consensus motif sequence: 5′-RRRCWWGYYYRRRCWW[G/T]YYY-3′. According to the data from the HapMap project, the SNP is common in African and Caucasian populations (MAF = 20%, confirmed by our genotyping analysis), but extremely rare in Asian populations (Chinese and Japanese) (MAF = 1%).
PRKAG2 encodes the gamma two noncatalytic subunit of the AMPK protein complex, a central sensor of energy stress. The known involvement of AMPK and p53 in cancer development and its interesting frequency pattern in different populations encouraged us to characterize the molecular function of this germ-line p53 binding motif polymorphism in cancer development.
Functional characterization of the binding site and its germ-line polymorphism (rs1860746)
To characterize the molecular function of this p53 binding site and its polymorphism, we chose lymphoblastoid cell lines (LCLs) as in vitro system because LCLs have a normal diploid genome and a large collection of cell lines where cells carrying different genotypes of germ-line SNPs are available for functional analysis. Further, western blot analysis showed that the p53 protein in LCLs could be induced in a time-dependent fashion by 5FU treatment (Supplementary Fig. 2).
In six different lymphoblastoid cell lines (three with the TT genotype, and three with the GG genotype), the PRKAG2 gene, however, did not change in expression after p53 induction with 5FU regardless of the genotype at the rs1860746 locus (Supplementary Fig. 4, Panel A). Moreover, no protein product of the PRKAG2 gene could be detected in the cell lines (data not shown). In contrast, p21 (CDKN1A) showed increased expression at each time point following 5FU treatment, demonstrating that p53 was functionally induced in these cell lines (Supplementary Fig. 4, Panel B). We surmise that either the binding site at the rs1860746 locus does not regulate the PPKAG2 gene transcription or that this regulation is silent in lymphoblastoid cell lines. Furthermore, after treatment with 5FU, no induction of PRKAG2 by p53 was observed in the HCT116 cell line that harbors wild-type p53 and is responsive to p53 action (Tan et al. 2005) (data not shown). Taken together, our results show that though the binding site at the rs1860746 locus binds p53 and can be used as a p53 responsive enhancer, it does not regulate PRKAG2.
Association analysis of rs1860746 in breast cancer
Analysis of the association of SNP with cancer susceptibility under a recessive model of inheritance in the combined Swedish and Finnish samples
Genotype Freq (%)
OR (95% CI)
GG or GT
1.34 (1.01, 1.77)
1.26 (0.92, 1.72)
1.48 (0.93, 2.35)
1.30 (0.96, 1.76)
1.66 (1.00, 2.75)
1.25 (0.92, 1.70)
1.48 (1.01, 2.17)
To further validate the association, we then genotyped rs1860746 in another three breast cancer case–control samples of European origin (ABCFS, GENICA, and KCONFAB), consisting of additional 2,615 cases and 2,458 controls. The joint analysis of all the four samples with ER status information (consisting of 4,190 cases and 5,197 controls) showed the significant association with ER negative breast cancer (OR = 1.47 (95%CI = 1.02–2.12), P = 0.038) (Fig. 3), while consistent association was observed across all the four samples. In contrast, no consistent association was observed across all the independent samples for the overall breast cancer risk as well as other patient subgroups (Fig. 3, Supplement Fig. 5).
This study presents one of the few efforts where p53-related regulatory variants were investigated molecularly and genetically (Pietsch et al. 2006). In addition to the T/G polymorphism within the intronic promoter of MDM2 (Bond et al. 2004), Mendendez et al. (2007) also identified a C/T polymorphism within the proximal promoter region of the flt-1 gene, where the minor allele of T created a half-binding site for p53 and brought the system under the control of p53 network. A more recent effort by the same group has further demonstrated that the presence of this polymorphism also created a partial responsiveness to estrogen receptor upstream of the previously identified binding half-site for p53. This results in synergistic simulation of transcription at this flt-promoter site through the combined action of p53 and ER (Menendez et al. 2007). The importance of these p53-related regulatory variants in disease development, however, has not been demonstrated.
We sought to identify potential regulatory SNPs by a “forward” genetic strategy that first assesses all DNA binding sites of p53 in a genome wide manner, mines polymorphisms within the binding sites, interrogates the functional impact of these SNPs on the primary property of p53 occupancy and transcriptional regulation, and lastly investigates their association with disease susceptibility. As a result of the initial attempt, we found that the homozygous state of the minor allele (TT) of one such binding site variant, rs1860746, showed significantly lower p53 occupancy after cellular induction with a genotoxic agent. Given the known function of p53 as an important tumor suppressor gene, and the placement of the binding site variant within another cancer related gene PRKAG2 (encoding AMPKγ) (Inoki et al. 2003; Shaw et al. 2004; Jones et al. 2005; Laderoute et al. 2006), we sought to determine the association of this SNP with cancer susceptibility in breast cancer. Our results show a modest effect of the homozygous TT state on breast cancer susceptibility which is significant only in ER negative breast cancers after examining over 5,000 cases and controls. Such modest effects are intriguing but not definitive and therefore will require larger studies to validate, especially since the frequency of the effective homozygous state is low (<5%). This is similar to the results of SNP rs3020314 which tags a region of ESR1 intron 4 (the estrogen receptor gene) where after analysis in 55,000 cases and controls showed an OR effect of 1.05 confined to women bearing ER positive tumors (Dunning et al. 2009). The greater association of the homozygous TT genotype of rs1860746 with susceptibility for ER negative cancers is consistent with the molecular understanding of breast cancer biology since ER negative tumors have greater aneuploidy and are associated with aberrations of p53 itself (Miller et al. 2005). Carriers of germ-line p53 mutations in the families affected with Li-Fraumeni syndromes (LFS) are at risk for early-onset breast cancer (Olivier et al. 2003), and our findings further suggest that genetic disturbances in downstream transcriptional regulation by p53 may also have an effect on breast cancer risk. We also want to point out that BRCA mutation carriers have been excluded from the familial patients from the KConFab and HEBC studies. In familial patients, BRCA mutations, especially BRCA1 mutations, would be a strong confounding risk factor for ER negative breast cancer, if not excluded. Therefore, by excluding BRCA carriers, our association results are expected to be independent from the confounding effect of BRCA mutations. Further studies will be needed to investigate the risk effect of the polymorphism in BRCA mutation carriers.
Despite the definitive binding of p53 at the rs1860746 locus, the transcriptional analysis of the PRKAG2 gene, however, did not show direct regulation of this gene by p53 either in lymphoblastoid cell lines or in HCT116 colon carcinoma cell line. This discrepancy can be due to different scenarios. First, the p53 binding site at the rs1860746 locus may regulate another gene in the vicinity in a p53 dependent manner through distant regulatory control which we have recently demonstrated with the estrogen receptor (Fullwood et al. 2009). Second, as the most conservative explanation, rs1860746 may be in linkage disequilibrium with another causal mutation within the PRKAG2 gene or another gene in the vicinity and that the differential p53 binding was a fortuitous but irrelevant observation. It should also be noted that though the effect size of the rs1860746 SNP in breast cancer is small, it may be greater in other cancer types that are more p53 driven, as suggested by our subgroup analysis in breast cancer.
Our study also raises an interesting facet about potential causal regulatory SNPs with low effect size. We could see a signal in our genetic analysis only using a recessive model which would have been missed by standard GWAS analyses where either allele or trend association are usually tested. The functional assignment of a regulatory SNP allows for the selection of the appropriate analytical approach. Moreover, it raises yet another tier of genetic polymorphisms that may contribute to disease susceptibility: one of low effect size and recessive in nature. As proof-of-principal, our study has highlighted that combining the genome-wide discovery of transcription regulatory elements (such as transcription factor binding sites) with the forward genetic analysis in both model and human systems can greatly advance our understanding on the molecular and physiological functions of regulatory genetic variation. We further posit that intersect between the new genome-wide knowledge of various regulatory sequences and the rapidly accumulated disease association data on germ-line polymorphisms will bring new insights to the role of genetic variants in regulatory variation in human populations.
First, we wish to thank all the women who took the time and effort to participate in this study. We would like to thank: Anna Christensson and Boel Bissmarck for obtaining consent and coordinating the collecting of the Swedish samples; Lena U. Rosenberg, Mattias Hammarström and Eija Flygare for reviewing medical records of the Swedish samples; Christer Halldén at Swegene laboratories, Malmö, Sweden, for overseeing the DNA isolation from the Swedish blood samples; Lim Siew Lan and Irene Chen for isolating DNA from Swedish paraffin-embedded tissue samples; Ong Eng Hu Jason for genotyping; RN Kirsi Leinonen for sample and data collection of the Finnish samples. We wish to thank Heather Thorne, Eveline Niedermayr, all the kConFab research nurses and staff, the heads and staff of the Family Cancer Clinics, and the Clinical Follow Up Study (funded by NHMRC grants 145684, 288704 and 454508) for their contributions to this resource, and the many families who contribute to kConFab. Finnish Cancer Registry is gratefully acknowledged for providing cancer data. We also give our thanks to Dr Bert Vogelstein at the John Hopkins School of Medicine for providing the p53-null HCT116 cell line. This work was supported by funding from the Agency for Science & Technology and Research of Singapore (A*STAR), the National Institute of Health (grant number R01 CA 104021), the United States Army (Prime Award No. W81XWH-05-1-0314), the Academy of Finland (110663), Finnish Cancer Society, Helsinki University Central Hospital Research Fund, the Sigrid Juselius Fund and the Nordic Cancer Union. kConFab is supported by grants from the National Breast Cancer Foundation, the National Health and Medical Research Council (NHMRC) and by the Queensland Cancer Fund, the Cancer Councils of New South Wales, Victoria, Tasmania and South Australia, and the Cancer Foundation of Western Australia. The Australian Breast Cancer Family Study was supported by the National Cancer Institute, National Institutes of Health under RFA-CA-06-503 and through cooperative agreements with members of the Breast Cancer Family Registry and Principal Investigators, including University of Melbourne (U01 CA69638). The content of this manuscript does not necessarily reflect the views or policies of the National Cancer Institute or any of the collaborating centers in the BCFR, nor does mention of trade names, commercial products, or organizations imply endorsement by the US Government or the BCFR. The GENICA study was supported by the Federal Ministry of Education and Research (BMBF) Germany grants and 01KW9975/5, 01KW9976/8, 01KW9977/0, 01KW0114 the Robert Bosch Foundation, Stuttgart, Department of Internal Medicine, Evangelische Kliniken Bonn gGmbH, Johanniter Krankenhaus, Bonn, Deutsches Krebsforschungszentrum (DKFZ), Heidelberg, and Research Institute of Occupational Medicine of the German Social Accident Insurance (BGFA), Bochum, Germany. All authors declare no competing interests exists.
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