BAP1 loss defines a new class of renal cell carcinoma.

Abstract:

:The molecular pathogenesis of renal cell carcinoma (RCC) is poorly understood. Whole-genome and exome sequencing followed by innovative tumorgraft analyses (to accurately determine mutant allele ratios) identified several putative two-hit tumor suppressor genes, including BAP1. The BAP1 protein, a nuclear deubiquitinase, is inactivated in 15% of clear cell RCCs. BAP1 cofractionates with and binds to HCF-1 in tumorgrafts. Mutations disrupting the HCF-1 binding motif impair BAP1-mediated suppression of cell proliferation but not deubiquitination of monoubiquitinated histone 2A lysine 119 (H2AK119ub1). BAP1 loss sensitizes RCC cells in vitro to genotoxic stress. Notably, mutations in BAP1 and PBRM1 anticorrelate in tumors (P = 3 × 10(-5)), [corrected] and combined loss of BAP1 and PBRM1 in a few RCCs was associated with rhabdoid features (q = 0.0007). BAP1 and PBRM1 regulate seemingly different gene expression programs, and BAP1 loss was associated with high tumor grade (q = 0.0005). Our results establish the foundation for an integrated pathological and molecular genetic classification of RCC, paving the way for subtype-specific treatments exploiting genetic vulnerabilities.

journal_name

Nat Genet

journal_title

Nature genetics

authors

Peña-Llopis S,Vega-Rubín-de-Celis S,Liao A,Leng N,Pavía-Jiménez A,Wang S,Yamasaki T,Zhrebker L,Sivanand S,Spence P,Kinch L,Hambuch T,Jain S,Lotan Y,Margulis V,Sagalowsky AI,Summerour PB,Kabbani W,Wong SW,Grishin N,

doi

10.1038/ng.2323

subject

Has Abstract

pub_date

2012-06-10 00:00:00

pages

751-9

issue

7

eissn

1061-4036

issn

1546-1718

pii

ng.2323

journal_volume

44

pub_type

杂志文章
  • A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes.

    abstract::We report that a single-nucleotide polymorphism (SNP) in the gene (PTPN22) encoding the lymphoid protein tyrosine phosphatase (LYP), a suppressor of T-cell activation, is associated with type 1 diabetes mellitus (T1D). The variants encoded by the two alleles, 1858C and 1858T, differ in a crucial amino acid residue inv...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1323

    authors: Bottini N,Musumeci L,Alonso A,Rahmouni S,Nika K,Rostamkhani M,MacMurray J,Meloni GF,Lucarelli P,Pellecchia M,Eisenbarth GS,Comings D,Mustelin T

    更新日期:2004-04-01 00:00:00

  • A brief history of gene therapy.

    abstract::The concepts of gene therapy arose initially during the 1960s and early 1970s whilst the development of genetically marked cells lines and the clarification of mechanisms of cell transformation by the papaovaviruses polyoma and SV40 was in progress. With the arrival of recombinant DNA techniques, cloned genes became a...

    journal_title:Nature genetics

    pub_type: 历史文章,杂志文章,评审

    doi:10.1038/ng1092-93

    authors: Friedmann T

    更新日期:1992-10-01 00:00:00

  • Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome.

    abstract::Alström syndrome (OMIM 203800) is an autosomal recessive disease, characterized by cone-rod retinal dystrophy, cardiomyopathy and type 2 diabetes mellitus, that has been mapped to chromosome 2p13 (refs 1-5). We have studied an individual with Alström syndrome carrying a familial balanced reciprocal chromosome transloc...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng874

    authors: Hearn T,Renforth GL,Spalluto C,Hanley NA,Piper K,Brickwood S,White C,Connolly V,Taylor JF,Russell-Eggitt I,Bonneau D,Walker M,Wilson DI

    更新日期:2002-05-01 00:00:00

  • EGFR signaling attenuates Groucho-dependent repression to antagonize Notch transcriptional output.

    abstract::Crosstalk between signaling pathways is crucial for the generation of complex and varied transcriptional networks. Antagonism between the EGF-receptor (EGFR) and Notch pathways in particular is well documented, although the underlying mechanism is poorly understood. The global corepressor Groucho (Gro) and its transdu...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1486

    authors: Hasson P,Egoz N,Winkler C,Volohonsky G,Jia S,Dinur T,Volk T,Courey AJ,Paroush Z

    更新日期:2005-01-01 00:00:00

  • Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis.

    abstract::Chronic pancreatitis (CP) is a continuing or relapsing inflammatory disease of the pancreas. In approximately one-third of all cases, no aetiological factor can be found, and these patients are classified as having idiopathic disease. Pathophysiologically, autodigestion and inflammation may be caused by either increas...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/76088

    authors: Witt H,Luck W,Hennies HC,Classen M,Kage A,Lass U,Landt O,Becker M

    更新日期:2000-06-01 00:00:00

  • Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families.

    abstract::The hereditary breast cancer gene BRCA2 was recently cloned and is believed to account for almost half of site-specific breast cancer families and the majority of male breast cancer families. We screened 49 site-specific breast cancer families for mutations in the BRCA2 gene using single strand conformation analysis (...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng0596-120

    authors: Phelan CM,Lancaster JM,Tonin P,Gumbs C,Cochran C,Carter R,Ghadirian P,Perret C,Moslehi R,Dion F,Faucher MC,Dole K,Karimi S,Foulkes W,Lounis H,Warner E,Goss P,Anderson D,Larsson C,Narod SA,Futreal PA

    更新日期:1996-05-01 00:00:00

  • Establishment of functional imprinting of the H19 gene in human developing placentae.

    abstract::We have found that the imprinted H19 gene can be expressed either biallelically or monoallelically in the developing human placentae. H19 biallelic expression is confined to the placenta until 10 weeks of gestation, after which it becomes exclusively maternal, and does not affect allele-specificity or levels of IGF2 e...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng0795-318

    authors: Jinno Y,Ikeda Y,Yun K,Maw M,Masuzaki H,Fukuda H,Inuzuka K,Fujishita A,Ohtani Y,Okimoto T

    更新日期:1995-07-01 00:00:00

  • Contribution of the FMR1 gene mutation to human intellectual dysfunction.

    abstract::The degree to which genetic factors influence human intelligence remains a matter of some controversy. However, there is little doubt that single gene mutations can significantly alter brain development and function. For example, mutations affecting the FMR1 gene cause the fragile X syndrome, the most prevalent known ...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1195-331

    authors: Reiss AL,Freund LS,Baumgardner TL,Abrams MT,Denckla MB

    更新日期:1995-11-01 00:00:00

  • Activating SRC mutation in a subset of advanced human colon cancers.

    abstract::The discovery of Rous sarcoma virus (RSV) led to the identification of cellular Src (c-Src), a non-receptor tyrosine kinase, which has since been implicated in the development of numerous human cancers. c-Src has been found to be highly activated in colon cancers, particularly in those metastatic to the liver. Studies...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/5971

    authors: Irby RB,Mao W,Coppola D,Kang J,Loubeau JM,Trudeau W,Karl R,Fujita DJ,Jove R,Yeatman TJ

    更新日期:1999-02-01 00:00:00

  • The apolipoprotein(a) gene is regulated by sex hormones and acute-phase inducers in YAC transgenic mice.

    abstract::High plasma concentrations of apolipoprotein (a) (apo(a)) have been implicated as a major independent risk factor for atherosclerosis in humans. Apo(a) is a large, evolutionarily new gene (present primarily in primates) for which considerable controversy exists concerning the factors that regulate its expression. To i...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng0495-424

    authors: Frazer KA,Narla G,Zhang JL,Rubin EM

    更新日期:1995-04-01 00:00:00

  • SMAD4-deficient intestinal tumors recruit CCR1+ myeloid cells that promote invasion.

    abstract::Inactivation of TGF-beta family signaling is implicated in colorectal tumor progression. Using cis-Apc(+/Delta716) Smad4(+/-) mutant mice (referred to as cis-Apc/Smad4), a model of invasive colorectal cancer in which TGF-beta family signaling is blocked, we show here that a new type of immature myeloid cell (iMC) is r...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1997

    authors: Kitamura T,Kometani K,Hashida H,Matsunaga A,Miyoshi H,Hosogi H,Aoki M,Oshima M,Hattori M,Takabayashi A,Minato N,Taketo MM

    更新日期:2007-04-01 00:00:00

  • Identification of DOK genes as lung tumor suppressors.

    abstract::Genome-wide analyses of human lung adenocarcinoma have identified regions of consistent copy-number gain or loss, but in many cases the oncogenes and tumor suppressors presumed to reside in these loci remain to be determined. Here we identify the downstream of tyrosine kinase (Dok) family members Dok1, Dok2 and Dok3 a...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng.527

    authors: Berger AH,Niki M,Morotti A,Taylor BS,Socci ND,Viale A,Brennan C,Szoke J,Motoi N,Rothman PB,Teruya-Feldstein J,Gerald WL,Ladanyi M,Pandolfi PP

    更新日期:2010-03-01 00:00:00

  • Distinct and overlapping functions of allelic forms of human mannose binding protein.

    abstract::Human mannose binding protein (MBP) is a C-type serum lectin involved in first-line host defense against a variety of bacterial, fungal and viral pathogens. Recently an association was found between low levels of serum MBP and an increased frequency of recurrent infections in infants. A particular genotype, in which g...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng0992-50

    authors: Super M,Gillies SD,Foley S,Sastry K,Schweinle JE,Silverman VJ,Ezekowitz RA

    更新日期:1992-09-01 00:00:00

  • A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.

    abstract::Epileptic disorders affect about 20-40 million people worldwide, and 40% of these are idiopathic generalized epilepsies (IGEs; ref. 1). Most of the IGEs that are inherited are complex, multigenic diseases. To address basic mechanisms for epilepsies, we have focused on one well-defined class of IGEs with an autosomal-d...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng0198-53

    authors: Charlier C,Singh NA,Ryan SG,Lewis TB,Reus BE,Leach RJ,Leppert M

    更新日期:1998-01-01 00:00:00

  • Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours.

    abstract::Testicular germ-cell tumours (TGCT) affect 1 in 500 men and are the most common cancer in males aged 15-40 in Western European populations. The incidence of TGCT has risen dramatically over the last century. Known risk factors for TGCT include a history of undescended testis (UDT), testicular dysgenesis, infertility, ...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/72877

    authors: Rapley EA,Crockford GP,Teare D,Biggs P,Seal S,Barfoot R,Edwards S,Hamoudi R,Heimdal K,Fossâ SD,Tucker K,Donald J,Collins F,Friedlander M,Hogg D,Goss P,Heidenreich A,Ormiston W,Daly PA,Forman D,Oliver TD,Leahy M

    更新日期:2000-02-01 00:00:00

  • Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice.

    abstract::Loss of tight association between epidermis and dermis underlies several blistering disorders and is frequently caused by impaired function of extracellular matrix (ECM) proteins. Here we describe a new protein in mouse, Fras1, that is specifically detected in a linear fashion underlying the epidermis and the basal su...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1168

    authors: Vrontou S,Petrou P,Meyer BI,Galanopoulos VK,Imai K,Yanagi M,Chowdhury K,Scambler PJ,Chalepakis G

    更新日期:2003-06-01 00:00:00

  • Nf1 deficiency causes Ras-mediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia.

    abstract::The Ras signal transduction pathway is often deregulated in human myeloid leukaemia. For example, activating point mutations in RAS genes are found in some patients with juvenile chronic myelogenous leukaemia (JCML), while other patients with JCML show loss of the neurofibromatosis type 1 (NF1) gene, a Ras GTPase acti...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng0296-137

    authors: Largaespada DA,Brannan CI,Jenkins NA,Copeland NG

    更新日期:1996-02-01 00:00:00

  • Testing for genetic associations in arbitrarily structured populations.

    abstract::We present a new statistical test of association between a trait and genetic markers, which we theoretically and practically prove to be robust to arbitrarily complex population structure. The statistical test involves a set of parameters that can be directly estimated from large-scale genotyping data, such as those m...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng.3244

    authors: Song M,Hao W,Storey JD

    更新日期:2015-05-01 00:00:00

  • Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy.

    abstract::We report germline missense mutations in ETV6 segregating with the dominant transmission of thrombocytopenia and hematologic malignancy in three unrelated kindreds, defining a new hereditary syndrome featuring thrombocytopenia with susceptibility to diverse hematologic neoplasms. Two variants, p.Arg369Gln and p.Arg399...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng.3177

    authors: Zhang MY,Churpek JE,Keel SB,Walsh T,Lee MK,Loeb KR,Gulsuner S,Pritchard CC,Sanchez-Bonilla M,Delrow JJ,Basom RS,Forouhar M,Gyurkocza B,Schwartz BS,Neistadt B,Marquez R,Mariani CJ,Coats SA,Hofmann I,Lindsley RC,Wil

    更新日期:2015-02-01 00:00:00

  • In vivo selection using a cell-growth switch.

    abstract::A major obstacle to stem-cell gene therapy rests in the inability to deliver a gene into a therapeutically relevant fraction of stem cells. One way to circumvent this obstacle is to use selection. Vectors containing two linked genes serve as the basis for selection, with one gene encoding a selectable product and the ...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/79194

    authors: Jin L,Zeng H,Chien S,Otto KG,Richard RE,Emery DW,Blau CA

    更新日期:2000-09-01 00:00:00

  • Common variants associated with general and MMR vaccine-related febrile seizures.

    abstract::Febrile seizures represent a serious adverse event following measles, mumps and rubella (MMR) vaccination. We conducted a series of genome-wide association scans comparing children with MMR-related febrile seizures, children with febrile seizures unrelated to vaccination and controls with no history of febrile seizure...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng.3129

    authors: Feenstra B,Pasternak B,Geller F,Carstensen L,Wang T,Huang F,Eitson JL,Hollegaard MV,Svanström H,Vestergaard M,Hougaard DM,Schoggins JW,Jan LY,Melbye M,Hviid A

    更新日期:2014-12-01 00:00:00

  • Specific interaction between genotype, smoking and autoimmunity to citrullinated alpha-enolase in the etiology of rheumatoid arthritis.

    abstract::Gene-environment associations are important in rheumatoid arthritis (RA) susceptibility, with an association existing between smoking, HLA- DRB1 'shared epitope' alleles, PTPN22 and antibodies to cyclic citrullinated peptides (CCP). Here, we test the hypothesis that a subset of the anti-CCP response, with specific aut...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng.480

    authors: Mahdi H,Fisher BA,Källberg H,Plant D,Malmström V,Rönnelid J,Charles P,Ding B,Alfredsson L,Padyukov L,Symmons DP,Venables PJ,Klareskog L,Lundberg K

    更新日期:2009-12-01 00:00:00

  • Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice.

    abstract::Peripheral myelin protein PMP22 has been suggested to have a role in peripheral nerve myelination and cell proliferation. Defects at the PMP22 locus are associated with peripheral neuropathies such as Charcot-Marie-Tooth disease type 1A. We now demonstrate that mice devoid of Pmp22 are retarded in the onset of myelina...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1195-274

    authors: Adlkofer K,Martini R,Aguzzi A,Zielasek J,Toyka KV,Suter U

    更新日期:1995-11-01 00:00:00

  • Evidence for genomic rearrangements mediated by human endogenous retroviruses during primate evolution.

    abstract::Human endogenous retroviruses (HERVs), which are remnants of past retroviral infections of the germline cells of our ancestors, make up as much as 8% of the human genome and may even outnumber genes. Most HERVs seem to have entered the genome between 10 and 50 million years ago, and they comprise over 200 distinct gro...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng775

    authors: Hughes JF,Coffin JM

    更新日期:2001-12-01 00:00:00

  • Widespread occurrence of alternative splicing at NAGNAG acceptors contributes to proteome plasticity.

    abstract::Splice acceptors with the genomic NAGNAG motif may cause NAG insertion-deletions in transcripts, occur in 30% of human genes and are functional in at least 5% of human genes. We found five significant biases indicating that their distribution is nonrandom and that they are evolutionarily conserved and tissue-specific....

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1469

    authors: Hiller M,Huse K,Szafranski K,Jahn N,Hampe J,Schreiber S,Backofen R,Platzer M

    更新日期:2004-12-01 00:00:00

  • Adenovirus mediated expression of therapeutic plasma levels of human factor IX in mice.

    abstract::Gene therapy strategies designed to combat haemophilia B, caused by defects in clotting factor IX, have so far concentrated on ex vivo approaches. We have now evaluated adenoviral vector-mediated expression of human factor IX in vivo. Injection of the vector Av1H9B, which encodes human factor IX cDNA, into the tail ve...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1293-397

    authors: Smith TA,Mehaffey MG,Kayda DB,Saunders JM,Yei S,Trapnell BC,McClelland A,Kaleko M

    更新日期:1993-12-01 00:00:00

  • Transcriptome analysis of the acoelomate human parasite Schistosoma mansoni.

    abstract::Schistosoma mansoni is the primary causative agent of schistosomiasis, which affects 200 million individuals in 74 countries. We generated 163,000 expressed-sequence tags (ESTs) from normalized cDNA libraries from six selected developmental stages of the parasite, resulting in 31,000 assembled sequences and 92% sampli...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1237

    authors: Verjovski-Almeida S,DeMarco R,Martins EA,Guimarães PE,Ojopi EP,Paquola AC,Piazza JP,Nishiyama MY Jr,Kitajima JP,Adamson RE,Ashton PD,Bonaldo MF,Coulson PS,Dillon GP,Farias LP,Gregorio SP,Ho PL,Leite RA,Malaquias LC,

    更新日期:2003-10-01 00:00:00

  • Genome-wide association study identifies three susceptibility loci for laryngeal squamous cell carcinoma in the Chinese population.

    abstract::To identify genetic markers for laryngeal squamous cell carcinoma (LSCC), we conducted a genome-wide association study (GWAS) on 993 individuals with LSCC (cases) and 1,995 cancer-free controls from Chinese populations. The most promising variants (association P < 1 × 10(-5)) were then replicated in 3 independent sets...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng.3090

    authors: Wei Q,Yu D,Liu M,Wang M,Zhao M,Liu M,Jia W,Ma H,Fang J,Xu W,Chen K,Xu Z,Wang J,Tian L,Yuan H,Chang J,Hu Z,Wei L,Huang Y,Han Y,Liu J,Han D,Shen H,Yang S,Zheng H,Ji Q,Li D,Tan W,Wu C,Lin D

    更新日期:2014-10-01 00:00:00

  • A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.

    abstract::Epilepsy affects at least 2% of the population at some time in their lives. The epilepsies are a heterogeneous group of disorders, many with an inherited component. Although specific genes have been identified in a few rare diseases causing seizures as part of a more diffuse brain disorder, the molecular pathology of ...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng1095-201

    authors: Steinlein OK,Mulley JC,Propping P,Wallace RH,Phillips HA,Sutherland GR,Scheffer IE,Berkovic SF

    更新日期:1995-10-01 00:00:00

  • Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.

    abstract::We genotyped 2,861 cases of primary biliary cirrhosis (PBC) from the UK PBC Consortium and 8,514 UK population controls across 196,524 variants within 186 known autoimmune risk loci. We identified 3 loci newly associated with PBC (at P<5×10(-8)), increasing the number of known susceptibility loci to 25. The most assoc...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng.2395

    authors: Liu JZ,Almarri MA,Gaffney DJ,Mells GF,Jostins L,Cordell HJ,Ducker SJ,Day DB,Heneghan MA,Neuberger JM,Donaldson PT,Bathgate AJ,Burroughs A,Davies MH,Jones DE,Alexander GJ,Barrett JC,Sandford RN,Anderson CA,UK Primary

    更新日期:2012-10-01 00:00:00