Contrasting effects of Deadend1 (Dnd1) gain and loss of function mutations on allelic inheritance, testicular cancer, and intestinal polyposis
© Zechel et al.; licensee BioMed Central Ltd. 2013
Received: 24 March 2013
Accepted: 7 June 2013
Published: 17 June 2013
Certain mutations in the Deadend1 (Dnd1) gene are the most potent modifiers of testicular germ cell tumor (TGCT) susceptibility in mice and rats. In the 129 family of mice, the Dnd1 Ter mutation significantly increases occurrence of TGCT-affected males. To test the hypothesis that he Dnd1 Ter allele is a loss-of-function mutation; we characterized the consequences of a genetically-engineered loss-of-function mutation in mice, and compared these results with those for Dnd1 Ter .
We found that intercrossing Dnd1 +/KO heterozygotes to generate a complete loss-of-function led to absence of Dnd1 KO/KO homozygotes and significantly reduced numbers of Dnd1 +/KO heterozygotes. Further crosses showed that Dnd1 Ter partially rescues loss of Dnd1 KO mice. We also found that loss of a single copy of Dnd1 in Dnd1 KO/+ heterozygotes did not affect baseline occurrence of TGCT-affected males and that Dnd1 Ter increased TGCT risk regardless whether the alternative allele was loss-of-function (Dnd1 KO ) or wild-type (Dnd1 + ). Finally, we found that the action of Dnd1 Ter was not limited to testicular cancer, but also significantly increased polyp number and burden in the Apc +/Min model of intestinal polyposis.
These results show that Dnd1 is essential for normal allelic inheritance and that Dnd1 Ter has a novel combination of functions that significantly increase risk for both testicular and intestinal cancer.
KeywordsTesticular cancer Allelic segregation Intestinal neoplasia DND1
Testicular germ cell tumors (TGCTs) are the most common cancer affecting young men. They are disproportionately represented in men aged 20–40, comprising ~60% of all cancers in this age group , while accounting for only 1.0-1.5 % of all cancers . The incidence of TGCTs has increased in the last 30 years , rising approximately 3% per year from 1972 to 2002  compared to an overall annual decrease of 0.6% from 1994–2009 for all cancers in men .
Testicular cancer is widely considered to be one of the most heritable forms of cancer [6, 7]. Genetic factors contribute significantly to TGCT susceptibility as exemplified by a 4- to 15-fold increased risk in the sons and brothers of affected men, respectively [8, 9]. With conventional inheritance however, risk should be similar in sons and brothers. The ~4-fold difference in occurrence of affected sons and brothers implies that other modes of inheritance are involved. Despite strong heritability, known genetic mutations and single nucleotide polymorphisms (SNPs) make only modest contributions to susceptibility, illustrating the genetically complex nature of this disease. The gr/gr deletion, which is a common cause of infertility in men, is associated with increased TGCT risk . But its contribution is modest, occurring in only 3% of TGCT cases with a family history and 1% of unaffected individuals . gr/gr results from a 1.6 Mb deletion at the AZFc locus at Yq11 of the human Y chromosome, a region that contains multiple copies of several genes that are involved in male germ cell development including DAZ (deleted in azospermia), BPY2 (basic charge, Y-linked 2) and CDY1 (chromodomain protein, Y-linked 1). Effects of the gr/gr deletion on germ cell development and differentiation are largely unknown.
Several single nucleotide polymorphisms (SNPs) are associated with increased TGCT risk in humans. In particular, six studies implicate SNPs that are associated with at least 14 genes: ATF7IP , BAK1, DMRT1, KITLG, SPRY4, TERT, HPGDS, MAD1L1, RFWD3, TEX14, RAD51C, PPM1E, DAZL and PRDM14[12–19]. Molecular mechanisms remain unclear, in part because many SNPs are located outside the coding region of the associated gene, and in part because the haplotype structure and sequence of these loci have not yet been fully reported. Interestingly, the TERT SNP is also associated with adenocarcinoma .
Certain mutations in the Dead End 1 (Dnd1) gene are potent modifiers of TGCT susceptibility in both mice and rats. In the mouse, the spontaneous Dnd1 Ter mutation significantly increases TGCT susceptibility in the 129 family of inbred mouse strains. In particular, Dnd1 Ter increases occurrence of TGCT-affected males from a baseline of ~5% in the 129S1/SvImJ strain to 17% in Dnd1 +/Ter heterozygotes and 94% in Dnd1 Ter/Ter homozygotes [21, 22]. The Ter mutation is a single base substitution in exon 3, 3′ to its single RNA recognition motif (RRM), that transforms an arginine residue to a premature stop codon (Figure 1, see also ). The Ter mutation has been proposed to produce an mRNA that is lost by nonsense-mediated degradation owing to the presence of the premature stop codon. This conclusion was based on northern blots of mRNA isolated from TGCTs in Dnd1 Ter/Ter males . But the tissue type (TGCTs) used in this study may not have been appropriate to assess the fate of Dnd1transcripts.
In the rat, a spontaneous mutation has been identified where a G to A substitution in exon 4 produces a premature stop codon that is thought to result in a 62 amino acid truncation at the C-terminus of the DND1 protein (Figure 1, see also ). This mutation leads to germ cell tumors in males and females as well as to spontaneous metastases.
Dnd1 has many unique functions. Dnd1 shares significant sequence similarity with A1cf, a gene that encodes the RNA binding subunit of the Apobec1 cytidine deaminase that edits specific sites in specific mRNAs . Interestingly, DND1 blocks access of specific miRNAs to their 3′ target in mRNAs such as p27, LATS2 and TDRD7. DND1 also binds several pluripotency factor mRNAs including Oct4, Sox2, Nanog and LIN28 , regulators of cell cycle including LATS2, TP53, p21 and p27[27, 28], apoptotic factors such as BCLX and BAX , and is a positive regulator of geminin mRNA translation through binding to its 3′ UTR . The role of DND1 in these functions and complexes is unknown. DND1 transports mRNA transcripts from germ cell nuclei to germ cell granules . Finally, Dnd1 is required for primordial germ cell (PGC) survival ; PGCs are the stem cell for TGCTs . Together these observations implicate Dnd1 in many aspects of RNA translation control.
The Dnd1 gene in mouse has four exons and encodes an α-isoform, which is 352 amino acids, and a β-isoform, which is 340 amino acids (Figure 1). These isoforms are derived through alternative splicing and differ by 12 amino acids at the amino-terminus of the protein. DND1-α is expressed in early embryos, whereas DND1-β is expressed in the germ cells of the adult testis . Both isoforms contain a single RNA recognition motif (RRM) and a highly conserved HRAAAMA motif (unpubl). This 7 amino acid motif is found in most orthologues of Dnd1 and A1cf (JHN, unpubl.). In zebrafish, ATPase activity has been attributed to a variant of this motif in Dnd1.
Several considerations suggest that the assumption that Dnd1 Ter leads to loss-of-function is erroneous. In vivo loss of function using morpholinos to reduce expression in zebrafish showed that Dnd1 is required for PGC survival , possibly through an ATPase activity . Although TGCTs have been reported in zebrafish [35–37], reduced Dnd1 expression was not sufficient for tumorigenesis. However, because genetic background strongly regulates TGCT susceptibility in mice and rats [23, 38–40], absence of TGCTs in the zebrafish study could implicate either the nature of the mutation or genetic background as critical elements determining tumorigenic outcome.
To test whether TGCT susceptibility depends on the nature of Dnd1 mutations, we generated a line of 129/SvImJ-Dnd KO mice. We found that deficiency of Dnd1 leads to highly biased allelic inheritance and that Dnd1 Ter partially restores normal inheritance. We also found that Dnd1 Ter acts distinctly from Dnd1 KO to increase TGCT risk in a dosage-dependent manner in 129S1/SvImJ males, whereas Dnd1 KO did not significantly affect susceptibility. Finally, recent work suggests that susceptibility to both TGCTs and intestinal polyposis share genetic predisposition  and that DND1 is normally expressed in the intestine [42–46]. We therefore tested whether Dnd1 Ter affects intestinal tumorigenesis and found that Dnd1 Ter significantly increases polyp number and burden in Apc +/Min mice.
Loss of Dnd1homozygotes and heterozygotes
Dnd1 +/KO intercross – genotype distribution at weaning
Dnd1 +/KO intercross – genotype distribution at embryonic day 3.5 (E3.5)
Dnd1 +/KO segregation in backcrosses versus intercrosses
No. Dnd1 +/+
No. Dnd1 +/KO *(expectations)
% expected number
Litter size can be used to determine whether unusual inheritance patterns result from embryonic lethality. Litter size should be reduced substantially if deficiency of some genotypes results from lethality. By contrast, if production of gametes or fertilization is biased towards particular alleles, litter sizes should not differ among the various crosses. However, despite significant deviation from the expected genotypic distributions (Table 1), litter sizes did not vary significantly among crosses (Table 3). These results argue against lethality as the cause of the unusual genotypic distributions.
Interaction between Dnd1 Ter and Dnd1 KO
Dnd1 mRNA levels in Dnd1 +/KO males
Germ cell numbers and fecundity in Dnd1-deficient males
We next sought to test whether Dnd1 Ter and Dnd1 KO alleles induce similar effects on PGC numbers in testes of heterozygous and wild-type littermates from the Dnd1 KO line. Testes from Dnd1 +/Ter males showed modest but significant reductions in germ cell numbers and testis weight [22, 49]. We weighed testes from 6–10 week old Dnd1 +/KO males and their wild-type (+/+) littermates to determine if they were phenotypically similar to those from Dnd1 +/Ter . Testes from wild-type males weighed an average of 4.43 ± 0.88g, which was similar to the average testes weight of 4.44 ± 0.69g in Dnd1 +/KO heterozygotes (Additional file 1: Figure S1A). These results suggest that germ cell numbers were not significantly reduced in Dnd1 +/KO males. Histological analysis confirmed these results for both Dnd1 +/Ter and Dnd1 +/KO males (Additional file 1: Figure S1B & C). Finally, both male and female heterozygotes for the Dnd1 KO allele were fertile as measured by the similar number of offspring produced in backcrosses to 129S1/SvImJ (Table 3). Together these results suggest that the Dnd1 KO allele did not negatively impact germ cell numbers or fertility.
Dnd1mutations and TGCT-affected males
Dnd1 genotype and occurrence of males affected with at least one spontaneous TGCT
Affected males (%)
Occurrence of TGCTs-affected males of various Dnd1 genotypes
Affected males (%) (%)
Dnd1 Ter and intestinal polyposis
TGCTs are the third most heritable form of cancer, with approximately 25% of the susceptibility being attributed to underlying genetic factors . The limited success in identifying genetic variants that account for a significant proportion of TGCT cases highlights the complex nature of TGCT susceptibility [54–56]. Discovery of the gr/gr deletion, together with validated SNPs in the ATF7IP , BAK1, DMRT1, KITLG, SPRY4, TERT, HPGDS, MAD1L1, RFWD3, TEX14, RAD51C, PPM1E, DAZL and PRDM14[12–19, 57]. Even with these findings however, the majority of inherited TGCT susceptibility remains unknown. In the mouse, several TGCT susceptibility genes have been identified, including Kit, Kitlg, Pten, Dmrt1, Eif2s2 and others (for a review, see ). Together these human and mouse genes implicate pathways and functions related to germ cell proliferation, PGC differentiation and cell cycle control in TGCT development. But much remains to be learned about the nature of mutations in these genes that lead to tumorigenesis and about the ways that these molecular changes disrupt these pathways.
The current study suggests that Dnd1 Ter is not a loss-of-function allele, but instead affects TGCT risk and embryonic development in distinct ways from Dnd1 KO , a true loss-of-function mutation. The location of the point mutation found within Dnd1 does not conform to the “position of an exon-exon junction rule” for non-sense mediated decay . The premature Ter stop codon is located 37 nucleotides upstream of the 3′-most exon-exon junction, within the 50–55 nucleotide range that fails to elicit nonsense-mediated decay (Figure 1). As a result, a translated DND1Ter protein could be created consisting of Dnd1 exons 1–2 and part of exon 3, with an intact RRM but a disrupted HRAAAMA. The RRM within DND1Ter may still recognize its target mRNAs, but any functional or regulatory capabilities normally derived from the deleted portion of DND1 would be absent. This supposition is supported by work with the rat DND1Ter mutation, where the GFP-DND1Ter fusion protein is detectable in Huh7 cells . The normal cellular processes that DND1Ter might disrupt are numerous because RNA binding proteins have diverse functions, including alternative splicing, RNA stability, miRNA regulation, and translation control [60–63]. To date, antibodies are not available for mouse DND1, thereby precluding many obvious studies.
Recent work revealed an essential role of a putative ATPase domain in DND1 (RAAAE) in PGC survival . This previously unannotated domain shares homology with RAAA (amino acids 178–181) in mouse DND1 where the arginine residue represents the amino acid substituted with a stop codon in Dnd1 Ter . Thus any ATPase activity in mouse DND1 possesses would be lost in DND1Ter. This region is also part of a larger motif in DND1, HRAAAMA, which is highly conserved and found in many paralogous RNA binding proteins, including Apobec complementation factor (A1CF), suggesting that this motif is functionally important in this gene family (unpubl.).
Although DND1Ter appears to be a novel variant that increases TGCT risk, its tumorigenic effects are limited to the 129 strain of mice, which is not surprising, since this is the mouse strain that is susceptible to spontaneous TGCTs [38, 63]. This finding highlights the importance of genetic background on TGCT susceptibility, which has been observed in humans, particularly in the disparate TGCT rates among ethnic groups [4, 64]. The importance of genetic background is also evident in the interaction of DND1Ter and mouse background. The 129 strain interacts positively with DND1Ter to increase TGCT risk, whereas C56BL/6J and other strains only exhibit phenotypes related to some but not all aspects of mutations in genes such as Kit, Kitl, Pten, Eif2s2I and other TGCT modifier genes, but not TGCTs [55, 65, 66]. However, the tumorigenic effects of Dnd1 Ter are not limited to PGC transformation in the 129 strain mice. C57BL/6J mice with the Apc Min mutation are highly susceptible to intestinal polyps . However, when mice are compound heterozygotes for both Apc Min and Dnd1 Ter , polyp numbers and polyp burden are significantly increased (Figure 3). These results suggest that DND1Ter affects pathways in both PGC transformation and intestinal polyposis.
Embryonic lethality is the usual interpretation for biased genotypic distributions in intercrosses, especially with complete loss of homozygous mutants. However this interpretation is difficult to reconcile with normal litter sizes. In particular, loss of ~50% of intercross progeny (Table 1) should lead to average litter sizes that are ~2 rather than ~4 pups per litter (Table 3). We are aware of very few examples where substantial embryonic lethality does not affect litter size . Instead, we propose that the unusual genotypic distributions result from biased allelic inheritance where specific combinations of oocyte and sperm are favored (or disfavored). Normal segregation in reciprocal backcrosses with the 129S1/SvImJ suggests that gametes are produced in sufficient numbers and are adequately functional (Table 3). Instead results for intercrosses suggest that deficits in both females and males are needed to bias allelic inheritance. Together these results suggest that the bias arises at fertilization. Interestingly, genetically and functionally related genes also show biased segregation, including Apobec1 and A1cf[47, 48]
The contrasting effects of different classes of Dnd1 mutations may explain why sequencing studies failed to yield mutations within DND1 in human TGCT cases [24, 25]. Complete loss of DND1 function is not sufficient to promote TGCT formation, even on the TGCT-susceptible 129S1/SvImJ inbred genetic background; reducing the chances that DND1 mutations play a significant role in human TGCTs. Results from zebrafish support this interpretation. Loss of Dnd1 inhibits PGC migration and results in PGC deficiency, but did not produce TGCTs . TGCTs have been previously reported in zebrafish [35, 49]. Dnd1 Ter homozygotes also show reduced migration and loss of PGCs, with typically less than 20 PGCs arriving to the presumptive fetal gonads . Instead, our results show that it is the loss of the carboxy-terminus of DND1 protein that increases TGCT risk. The role of DND1Ter in TGCT formation is further supported by recent results in a rat study where a spontaneous mutation producing a premature stop codon in exon 4, similar to DND1 Ter , resulted in TGCTs . To date, human DND1 mutations have not yet been reported that yield a similarly truncated DND1 protein.
Through intercrosses with mice carrying a complete loss of function Dnd1 KO allele our study showed that DND1 is necessary for embryonic viability and results in abnormal allelic segregation. We have further shown that Dnd1 Ter , previously believed to be a loss-of-function allele, is likely translated into a protein that retains some normal DND1 function. Crosses with the Dnd1 knockout and Ter alleles revealed that the effects of the Ter allele on TGCT incidence depend on Ter dosage. Expression of the Ter allele in an APC Min model of intestinal polyposis also significantly increased polyp burden. These results demonstrate that Dnd1 Ter enhances tumorigenesis in two separate mouse models of cancer.
This strain (JR002448, previously known as 129/SvImJ) was obtained from the Jackson Laboratory (Bar Harbor, ME, USA). All studies were conducted on this inbred genetic background.
ES cells with a targeted deletion of Dnd1 were generated from 129S6 mice by the Intrexon Corporation, (Blacksburg, VA). Exons 1–2 and most of exon 3 of Dnd1 were removed through homologous recombination (Additional file 2: Figure S2), and cells were negatively selected with thymidine kinase (TK) and diphtheria toxin A (DTA), and positively selected with neomycin. PCR was used to confirm homologous recombination in these cells. ES cells were then injected into blastocysts (Case Transgenic and Targeting Facility) and the resulting chimeras were backcrossed onto the 129S1/SvImJ strain for more than 10 generations.
C57BL/6J (B6; JR000664) and C57BL/6J-Apc +/Min (Apc +/Min ; JR002020) mice were purchased from the Jackson Laboratory (Bar Harbor, ME).
From birth to 30 days of age, all mice were fed an autoclaved standard laboratory diet (Purina 5010 LabDiet (Richmond, IN) and were provided autoclaved water ad libitum. All mice were maintained on a 12-h light/dark cycle at the Wolstein Research Facility (CWRU).
Procedures were approved and conducted in compliance with Institutional Animal Care and Use Committee (IACUC) standards at (CWRU).
Embryonic day 3.5 (E3.5) embryo cultures
Embryos from time-mated Dnd1 +/KO X Dnd1 +/KO pregnant females were flushed from the oviducts and uterine horns on embryonic day 3.5 (E3.5) and cultured as previously described . To obtain sufficient material for reproducible genotyping, embryos were cultured for 1 week in individual wells of a 24-well tissue culture plate
DNA for PCR genotyping was extracted from tail tissue (mice) or cell masses (E3.5 embryo cultures). The nucleotide substitution in the Ter mutation results in the creation of a Dde1 site that was used for genotyping . The Dnd1 KO allele was amplified using primers extending from exon 4 of Dnd1 into the neomycin gene of the targeting construct. The Dnd1 KO primers are: CTGCGTGTTCGAATTCGCCAATGA (F), ACAAAGAGAAACCCGGTCTCGGAA (R). Primers used for genotyping Apc +/Min were previously described .
Male mice between the ages of 4–16 weeks were surveyed for TGCTs. Tumor incidence was calculated as the percentage of males with at least one TGCT. Histological analysis (H&E staining, see below) was used to confirm any TGCTs that were ambiguous at autopsy.
Intestinal polyp survey
Mice were euthanized with cervical dislocation. The small and large intestines were immediately removed, flushed with cold PBS, and cut longitudinally for polyp measurements. Polyps were counted and cross-sectional diameter was measured in the small intestine and colon with a Leica MZ10F Modular Stereomicroscope. Individual polyp size and number were used to calculate a measure of total polyp mass for each mouse, and this measure was used as a surrogate for polyp burden.
Testes were fixed with 10% formalin for at least 48h. Tissues were then embedded in paraffin and sectioned (5 μm) at the Case Comprehensive Cancer Center Tissue Procurement and Histology Core facility (TPHC). Hematoxylin and eosin staining was done in the TPHC facility.
Quantitative real-time PCR
RNA was extracted from cells and tissues using the RNeasy micro- and mini-kits, respectively (Qiagen Inc., Valencia, CA) according to the manufacturer’s instructions and including an on-column DNAse treatment. RNA was reverse-transcribed using the qScript Synthesis Kit (Quanta BioSciences Inc., Gaithersburg, MD). Changes in relative expression were quantified with the Chromo4 real-time PCR system (MJ Research) and TaqMan primers to Dnd1(Invitrogen #Mm00849348) and normalized to 18S (Invitrogen #4319413E) using manufacturer protocols and reported as mean ± SEM.
Data are presented as mean ± SEM. Two-tailed t-tests were used to evaluate results for quantitative PCR and data for both polyp numbers and burden. Chi-square contingency tests were used evaluate differences in occurrence of TGCT-affected males. Standard goodness-of-fit tests were used to evaluate differences between observed and Mendelian expectations for backcross and intercross segregation results. Then, to estimate the extent of loss for particular genotypes, the number of wild-type (+/+) mice (or embryos) was taken as the expected number for this genotypic class, and assuming Mendelian segregation (i.e. 1:2:1), the expected number of mutant heterozygotes and homozygotes was calculated. The difference between these observed and expected numbers was used to estimate the extent of loss for each genotypic class.
Testicular germ cell tumor
Single nucleotide polymorphism
RNA recognition motif
Primordial germ cell
Green fluorescent protein.
We thank Sabine Schaefer for her helpful comments on a draft of this paper. NCI grant CA75056 supported this work.
- Di PA, Vries EG, Gietema JA, Spierings DC, de JS: Testicular germ cell tumours: the paradigm of chemo-sensitive solid tumours. Int J Biochem Cell Biol. 2005, 37: 2437-2456.View Article
- Buetow SA: Epidemiology of testicular cancer. Epidemiol Rev. 1995, 17: 433-449.PubMed
- Bosl GJ, Motzer RJ: Testicular germ-cell cancer. N Engl J Med. 1997, 337: 242-253.View ArticlePubMed
- Chia VM, Quraishi SM, Devesa SS, Purdue MP, Cook MB, McGlynn KA: International trends in the incidence of testicular cancer, 1973–2002. Cancer Epidemiol Biomarkers Prev. 2010, 19: 1151-1159.PubMed CentralView ArticlePubMed
- Jemal A, Simard EP, Dorell C, Noone AM, Markowitz LE, Kohler B, Eheman C, Saraiya M, Bandi P, Saslow D: Annual report to the Nation on the Status of cancer, 1975–2009, Featuring the Burden and trends in Human Papillomavirus (HPV)−Associated cancers and HPV Vaccination coverage levels. J Natl Cancer Inst. 2013, 105: 175-201.PubMed CentralView ArticlePubMed
- Edsgard D, Dalgaard MD, Weinhold N, Wesolowska-Andersen A, Rajpert-De Meyts E, Ottesen AM, Juul A, Skakkebæk NE, Jensen TS, Gupta R: Genome-wide assessment of the association of rare and common copy number variations to testicular germ cell cancer. 2013, Endocrinology: Frontiers in, 4-
- Heimdal K, Olsson H, Tretli S, Fossa SD, Borresen AL, Bishop DT: A segregation analysis of testicular cancer based on Norwegian and Swedish families. Br J Cancer. 1997, 75: 1084-1087.PubMed CentralView ArticlePubMed
- Chia VM, Li Y, Goldin LR, Graubard BI, Greene MH, Korde L, Rubertone MV: Erickson RL. 2008, McGlynn KA: Risk of cancer in first- and second-degree relatives of testicular germ cell tumor cases and controls. Int J Cancer
- Neale RE, Carriere P, Murphy MF, Baade PD: Testicular cancer in twins: a meta-analysis. Br J Cancer. 2008, 98: 171-173.PubMed CentralView ArticlePubMed
- Hemminki K, Li X: Familial risk in testicular cancer as a clue to a heritable and environmental aetiology. Br J Cancer. 2004, 90: 1765-1770.PubMed CentralView ArticlePubMed
- Nathanson KL, Kanetsky PA, Hawes R, Vaughn DJ, Letrero R, Tucker K, Friedlander M, Phillips KA, Hogg D, Jewett MA, et al: The Y deletion gr/gr and susceptibility to testicular germ cell tumor. Am J Hum Genet. 2005, 77: 1034-1043.PubMed CentralView ArticlePubMed
- Turnbull C, Rapley EA, Seal S, Pernet D, Renwick A, Hughes D, Ricketts M, Linger R, Nsengimana J, Deloukas P, et al: Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer. Nat Genet. 2010, 42: 604-607.PubMed CentralView ArticlePubMed
- Kratz CP, Han SS, Rosenberg PS, Berndt SI, Burdett L, Yeager M, Korde LA, Mai PL, Pfeiffer R, Greene MH: Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour. J Med Genet. 2011, 48: 473-476.PubMed CentralView ArticlePubMed
- Poynter JN, Hooten AJ, Frazier AL, Ross JA: Associations between variants in KITLG, SPRY4, BAK1, and DMRT1 and pediatric germ cell tumors. Genes Chromosomes Cancer. 2012, 51: 266-271.View ArticlePubMed
- Rapley EA, Turnbull C, Al Olama AA, Dermitzakis ET, Linger R, Huddart RA, Renwick A, Hughes D, Hines S, Seal S, et al: A genome-wide association study of testicular germ cell tumor. Nat Genet. 2009, 41: 807-810.PubMed CentralView ArticlePubMed
- Kanetsky PA, Mitra N, Vardhanabhuti S, Vaughn DJ, Li M, Ciosek SL, Letrero R, D’Andrea K, Vaddi M, Doody DR, et al: A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility. Hum Mol Genet. 2011, 20: 3109-3117.PubMed CentralView ArticlePubMed
- Kanetsky PA, Mitra N, Vardhanabhuti S, Li M, Vaughn DJ, Letrero R, Ciosek SL, Doody DR, Smith LM, Weaver J, et al: Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer. Nat Genet. 2009, 41: 811-815.PubMed CentralView ArticlePubMed
- Chung CC, Kanetsky PA, Wang Z, Hildebrandt MA, Koster R, Skotheim RI, Kratz CP, Turnbull C, Cortessis VK, Bakken AC: Meta-analysis identifies four new loci associated with testicular germ cell tumor. Nat Genet. 2013, 45: 680-685.View ArticlePubMed
- Ruark E, Seal S, McDonald H, Zhang F, Elliot A, Lau K, Perdeaux E, Rapley E, Eeles R, Peto J: Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14. Nat Genet. 2013, 45: 686-689.View ArticlePubMed
- Kohno T, Kunitoh H, Shimada Y, Shiraishi K, Ishii Y, Goto K, Ohe Y, Nishiwaki Y, Kuchiba A, Yamamoto S: Individuals susceptible to lung adenocarcinoma defined by combined HLA-DQA1 and TERT genotypes. Carcinogenesis. 2010, 31: 834-841.View ArticlePubMed
- Noguchi T, Noguchi M: A recessive mutation (ter) causing germ cell deficiency and a high incidence of congenital testicular teratomas in 129/Sv-ter mice. J Natl Cancer Inst. 1985, 75: 385-392.PubMed
- Youngren KK, Coveney D, Peng X, Bhattacharya C, Schmidt LS, Nickerson ML, Lamb BT, Deng JM, Behringer RR, Capel B, et al: The Ter mutation in the dead end gene causes germ cell loss and testicular germ cell tumours. Nature. 2005, 435: 360-364.PubMed CentralView ArticlePubMed
- Northrup E, Zschemisch NH, Eisenblatter R, Glage S, Wedekind D, Cuppen E, Dorsch M, Hedrich HJ: The ter mutation in the rat Dnd1 gene initiates gonadal teratomas and infertility in both genders. PLoS One. 2012, 7: e38001-PubMed CentralView ArticlePubMed
- Sijmons RH, Vos YJ, Herkert JC, Bos KK, Holzik MF, Hoekstra-Weebers JE, Hofstra RM, Hoekstra HJ: Screening for germline DND1 mutations in testicular cancer patients. Fam Cancer. 2010, 9: 439-442.PubMed CentralView ArticlePubMed
- Linger R, Dudakia D, Huddart R, Tucker K, Friedlander M, Phillips KA, Hogg D, Jewett MA, Lohynska R, Daugaard G, et al: Analysis of the DND1 gene in men with sporadic and familial testicular germ cell tumors. Genes Chromosomes Cancer. 2008, 47: 247-252.PubMed CentralView ArticlePubMed
- Kedde M, Strasser MJ, Boldajipour B, Oude Vrielink JA, Slanchev K, Le SC, Nagel R, Voorhoeve PM, Van DJ, Orom UA, et al: RNA-binding protein Dnd1 inhibits microRNA access to target mRNA. Cell. 2007, 131: 1273-1286.View ArticlePubMed
- Zhu R, Iacovino M, Mahen E, Kyba M, Matin A: Transcripts that associate with the RNA binding protein, DEAD-END (DND1), in embryonic stem (ES) cells. BMC Mol Biol. 2011, 12: 37-PubMed CentralView ArticlePubMed
- Cook MS, Munger SC, Nadeau JH, Capel B: Regulation of male germ cell cycle arrest and differentiation by DND1 is modulated by genetic background. Development. 2011, 138: 23-32.PubMed CentralView ArticlePubMed
- Chen S, Zeng M, Sun H, Deng W, Lu Y, Tao D, Liu Y, Zhang S, Ma Y: Zebrafish Dnd protein binds to 3′UTR of geminin mRNA and regulates its expression. BMB Rep. 2010, 43: 438-444.View ArticlePubMed
- Slanchev K, Stebler J, Goudarzi M, Cojocaru V, Weidinger G, Raz E: Control of Dead end localization and activityΓÇôImplications for the function of the protein in antagonizing miRNA function. Mech Dev. 2009, 126: 270-277.View ArticlePubMed
- Weidinger G, Stebler J, Slanchev K, Dumstrei K, Wise C, Lovell-Badge R, Thisse C, Thisse B, Raz E: dead end, a novel vertebrate germ plasm component, is required for zebrafish primordial germ cell migration and survival. Curr Biol. 2003, 13: 1429-1434.View ArticlePubMed
- Stevens LC: Origin of testicular teratomas from primordial germ cells in mice. J Natl Cancer Inst. 1967, 38: 549-552.PubMed
- Bhattacharya C, Aggarwal S, Zhu R, Kumar M, Zhao M, Meistrich ML, Matin A: The mouse dead-end gene isoform alpha is necessary for germ cell and embryonic viability. Biochem Biophys Res Commun. 2007, 355: 194-199.PubMed CentralView ArticlePubMed
- Liu W, Collodi P: Zebrafish dead end possesses ATPase activity that is required for primordial germ cell development. FASEB J. 2010, 24: 2641-2650.PubMed CentralView ArticlePubMed
- Neumann JC, Chandler GL, Damoulis VA, Fustino NJ, Lillard K, Looijenga L, Margraf L, Rakheja D, Amatruda JF: Mutation in the type IB bone morphogenetic protein receptor alk6b impairs germ-cell differentiation and causes germ-cell tumors in zebrafish. Proc Natl Acad Sci. 2011, 108: 13153-13158.PubMed CentralView ArticlePubMed
- Neumann JC, Lillard K, Damoulis V, Amatruda JF: Zebrafish Models of Germ Cell Tumor. The Zebrafish: Disease Models and Chemical Screens. Edited by: Detrich HW, Westerfield M, Zon LI. 2011, San Diego: Academic Press, 4-24. 3
- Gill JA, Lowe L, Nguyen J, Liu PP, Blake T, Venkatesh B, Aplan PD: Enforced Expression of Simian Virus 40 Large T-Antigen Leads to Testicular Germ Cell Tumors in Zebrafish. Zebrafish. 2010, 7: 333-341.PubMed CentralView ArticlePubMed
- Stevens LC, Hummel KP: A description of spontaneous congenital testicular teratomas in strain 129 mice. J Natl Cancer Inst. 1957, 18: 719-747.PubMed
- Stevens LC: A new inbred subline of mice (129-terSv) with a high incidence of spontaneous congenital testicular teratomas. J Natl Cancer Inst. 1973, 50: 235-242.PubMed
- Stevens LC: Mackensen. 1961, Genetic and environmental influences on teratocarcinogenesis in mice:: JA
- Castillejo A, Sanchez-Heras AB, Jover R, Castillejo MI, Guarinos C, Oltra S, Martinez-Canto A, Barbera VM, Laforga J, Paya A, et al: Recurrent testicular germ cell tumors in a family with MYH-associated polyposis. J Clin Oncol. 2012, 30: e216-e217.View ArticlePubMed
- Larsson E, Tremaroli V, Lee YS, Koren O, Nookaew I, Fricker A, Nielsen J, Ley RE, Bäckhed F: Analysis of gut microbial regulation of host gene expression along the length of the gut and regulation of gut microbial ecology through MyD88. Gut. 2012, 61: 1124-1131.PubMed CentralView ArticlePubMed
- Mutch DM, Crespy V, Clough J, Henderson CJ, Lariani S, Mansourian R, Moulin J, Wolf CR, Williamson G: Hepatic cytochrome P-450 reductase-null mice show reduced transcriptional response to quercetin and reveal physiological homeostasis between jejunum and liver. Am J Physiol Gastrointest Liver Physiol. 2006, 291: G63-G72.View ArticlePubMed
- Thorrez L, Laudadio I, Van Deun K, Quintens R, Hendrickx N, Granvik M, Lemaire K, Schraenen A, Van Lommel L, Lehnert S: Tissue-specific disallowance of housekeeping genes: the other face of cell differentiation. Genome Res. 2011, 21: 95-105.PubMed CentralView ArticlePubMed
- Saito S, Furuno A, Sakurai J, Sakamoto A, Park HR, Shin-ya K, Tsuruo T, Tomida A: Chemical genomics identifies the unfolded protein response as a target for selective cancer cell killing during glucose deprivation. Cancer Res. 2009, 69: 4225-4234.View ArticlePubMed
- Horst D, Chen J, Morikawa T, Ogino S, Kirchner T, Shivdasani RA: Differential WNT activity in colorectal cancer confers limited tumorigenic potential and is regulated by MAPK signaling. Cancer Res. 2012, 72: 1547-1556.PubMed CentralView ArticlePubMed
- Nelson VR, Heaney JD, Tesar PJ, Davidson NO, Nadeau JH: Transgenerational epigenetic effects of the Apobec1 cytidine deaminase deficiency on testicular germ cell tumor susceptibility and embryonic viability. Proc Natl Acad Sci. 2012, 109: E2766-E2773.PubMed CentralView ArticlePubMed
- Blanc V, Henderson JO, Newberry EP, Kennedy S, Luo J, Davidson NO: Targeted deletion of the murine apobec-1 complementation factor (acf) gene results in embryonic lethality. Mol Cell Biol. 2005, 25: 7260-7269.PubMed CentralView ArticlePubMed
- Collin GB, Asada Y, Varnum DS, Nadeau JH: DNA pooling as a quick method for finding candidate linkages in multigenic trait analysis: an example involving susceptibility to germ cell tumors. Mamm Genome. 1996, 7: 68-70.View ArticlePubMed
- Lam MY, Heaney JD, Youngren KK, Kawasoe JH, Nadeau JH: Trans-generational epistasis between Dnd1Ter and other modifier genes controls susceptibility to testicular germ cell tumors. Hum Mol Genet. 2007, 16: 2233-2240.View ArticlePubMed
- Zechel JL, MacLennan GT, Heaney JD, Nadeau JH: Spontaneous metastasis in mouse models of testicular germ-cell tumours. Int J Androl. 2011, 34: e278-e287.PubMed CentralView ArticlePubMed
- Detwiller KY, Fernando NT, Segal NH, Ryeom SW, D’Amore PA, Yoon SS: Analysis of hypoxia-related gene expression in sarcomas and effect of hypoxia on RNA interference of vascular endothelial cell growth factor A. Cancer Res. 2005, 65: 5881-5889.View ArticlePubMed
- Su LK, Kinzler KW, Vogelstein B, Preisinger AC, Moser AR, Luongo C, Gould KA, Dove WF: Multiple intestinal neoplasia caused by a mutation in the murine homolog of the APC gene. Science. 1992, 256: 668-670.View ArticlePubMed
- Kratz CP, Greene MH, Bratslavsky G, Shi J: A stratified genetic risk assessment for testicular cancer. Int J Androl. 2011, 34: e98-102.PubMed CentralView ArticlePubMed
- Lam MY, Youngren KK, Nadeau JH: Enhancers and suppressors of testicular cancer susceptibility in single- and double-mutant mice. Genetics. 2004, 166: 925-933.PubMed CentralView ArticlePubMed
- Stevens LC: The biology of teratomas. Adv Morphog. 1967, 6: 1-31.View ArticlePubMed
- Landi MT, Chatterjee N, Yu K, Goldin LR, Goldstein AM, Rotunno M, Mirabello L, Jacobs K, Wheeler W, Yeager M, et al: A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. Am J Hum Genet. 2009, 85: 679-691.PubMed CentralView ArticlePubMed
- Carouge D, Nadeau JH: Mouse Models of Testicular Germ Cell Tumors. Germ Cell Tumor. Edited by: Matin A. 2012, Manhattan: InTech, 75-106. 1
- Maquat LE: Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics. Nat Rev Mol Cell Biol. 2004, 5: 89-99.View ArticlePubMed
- Bandziulis RJ, Swanson MS, Dreyfuss G: RNA-binding proteins as developmental regulators. Genes Dev. 1989, 3: 431-437.View ArticlePubMed
- Fry DC, Kuby SA, Mildvan AS: ATP-binding site of adenylate kinase: mechanistic implications of its homology with ras-encoded p21, F1-ATPase, and other nucleotide-binding proteins. Proc Natl Acad Sci USA. 1986, 83: 907-911.PubMed CentralView ArticlePubMed
- Query CC, Bentley RC, Keene JD: A specific 31-nucleotide domain of U1 RNA directly interacts with the 70K small nuclear ribonucleoprotein component. Mol Cell Biol. 1989, 9: 4872-4881.PubMed CentralView ArticlePubMed
- Courage D, Nadeau JH: Mouse Models of Testicular Germ Cell Tumors. Germ Cell Tumor. Edited by: Matin A. 2012, InTech, 6-7-2012
- Testicular cancer - UK incidence statistics. http://info.cancerresearchuk.org/cancerstats/types/testis/incidence/uk-testicular-cancer-incidence-statistics,
- Zhu R, Heaney J, Nadeau JH, Ali S, Matin A: Deficiency of splicing factor 1 suppresses the occurrence of testicular germ cell tumors. Cancer Res. 2010, 70: 7264-7272.PubMed CentralView ArticlePubMed
- Krentz AD, Murphy MW, Zhang T, Sarver AL, Jain S, Griswold MD, Bardwell VJ, Zarkower D: Interaction between DMRT1 function and genetic background modulates signaling and pluripotency to control tumor susceptibility in the fetal germ line. Dev Biol. 2013, 377: 67-78.PubMed CentralView ArticlePubMed
- Moser AR, Pitot HC, Dove WF: A dominant mutation that predisposes to multiple intestinal neoplasia in the mouse. Science. 1990, 247: 322-324.View ArticlePubMed
- Landrock D, Atshaves BP, McIntosh AL, Landrock KK, Schroeder F, Kier AB: Acyl-CoA binding protein gene ablation induces pre-implantation embryonic lethality in mice. Lipids. 2010, 45: 567-580.PubMed CentralView ArticlePubMed
- Tesar PJ: Derivation of germ-line-competent embryonic stem cell lines from preblastocyst mouse embryos. Proc Natl Acad Sci USA. 2005, 102: 8239-8244.PubMed CentralView ArticlePubMed
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