Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MXI1

Identity

Hugo MXI1
Location 10q24-25

DNA/RNA

Description the gene spans approximately 60 kb; 6 exons
Transcription 2.6 kb mRNA; two transcription initiation sites

Protein

Description 228 amino acids; 26 kDa; contains a basic region/helix-loop-helix/leucine zipper (B-HLH-LZ) motif that is similar to that found in Myc family
Expression tissue specific; induced during cells terminal differentiation
Localisation nuclear
Function Mxil, discovered in 1993, is, with Mad, one of the proteins that can regulate Max, a human protein containing a basic helix-loop-helix leucine zipper (bHLH-zip) that allows the formation of cMyc-Max heterodimers and that activates transcription; Mad and Mxil may be involved in tumour suppression since they can compete with Myc proteins for the interaction with Max; Mxil normally functions to suppress cell growth: experimental induction of the gene resulted in the accumulation of cells in G2-M phase
Homology belongs to the basic helix-loop-helix (bhlh) family of transcription factors

Mutations

Somatic mutations have been described in some sporadic prostate cancers but no germline mutations were found in a study of 38 families with possible predisposition to this disease; a correlation between a polymorphic repeat in the 3' untranslated region in Mxil mRNA and regulation of its transcription and degradation has been suggested

Implicated in

Entity implicated in some sporadic cases of prostate cancer and glioblastoma as a tumour suppressor gene
  

External links

Nomenclature
HugoMXI1
GDBMXI1
Entrez_GeneMXI1  4601  MAX interactor 1
Cards
AtlasMXI1ID209
GeneCardsMXI1
EnsemblMXI1 [Search_View]   ENSG00000119950 [Gene_View]
GenatlasMXI1
GeneLynxMXI1
eGenomeMXI1
euGene4601
Genomic and cartography
GoldenPathMXI1  -     chr10:111975752-112037111 +  10q24-q25   [Description]    (hg18-Mar_2006)
EnsemblMXI1 - 10q24-q25 [CytoView]
NCBIMapview
OMIMDisease map [OMIM]
HomoloGeneMXI1
Gene and transcription
GenbankAA640393 [ ENTREZ ]
GenbankAA854855 [ ENTREZ ]
GenbankAI373426 [ ENTREZ ]
GenbankAI580132 [ ENTREZ ]
GenbankAL538051 [ ENTREZ ]
RefSeqNM_001008541 [ SRS ]    NM_001008541 [ ENTREZ ]
RefSeqNM_005962 [ SRS ]    NM_005962 [ ENTREZ ]
RefSeqNM_130439 [ SRS ]    NM_130439 [ ENTREZ ]
RefSeqAC_000053 [ SRS ]    AC_000053 [ ENTREZ ]
RefSeqNC_000010 [ SRS ]    NC_000010 [ ENTREZ ]
RefSeqNT_030059 [ SRS ]    NT_030059 [ ENTREZ ]
RefSeqNW_924884 [ SRS ]    NW_924884 [ ENTREZ ]
AceViewMXI1 AceView - NCBI
UnigeneHs.602078 [ SRS ]    Hs.602078 [ NCBI ]     HS602078 [ spliceNest ]
Fast-db16720 (alternative variants)
Protein : pattern, domain, 3D structure
SwissProtP50539 [ SRS]    P50539 [ EXPASY ]     P50539 [ INTERPRO ]
PrositePS50888 HLH [ SRS ]    PS50888 HLH [ Expasy ]
InterproIPR001092 HLH_basic [ SRS ]    IPR001092 HLH_basic [ EBI ]
InterproIPR011598 HLH_DNA_bd [ SRS ]    IPR011598 HLH_DNA_bd [ EBI ]
CluSTrP50539
PfamPF00010 HLH [ SRS ]    PF00010 HLH [ Sanger ]    pfam00010 [ NCBI-CDD ]
SmartSM00353 HLH [EMBL]
BlocksP50539
HPRD02486
Protein Interaction databases
DIPP50539
IntActP50539
Polymorphism : SNP, mutations, diseases
OMIM176807;600020    [ map ]   
GENECLINICS176807;600020
SNPMXI1 [dbSNP-NCBI]  
SNPNM_001008541 [SNP-NCI]  
SNPNM_005962 [SNP-NCI]  
SNPNM_130439 [SNP-NCI]  
SNPMXI1 [GeneSNPs - Utah]  MXI1] [HGBASE - SRS]
HAPMAPMXI1 [HAPMAP]  
COSMICMXI1 [Somatic mutation (COSMIC-CGP-Sanger)]  
HGMDMXI1
General knowledge
Family BrowserMXI1 [UCSC Family Browser]
SOURCENM_001008541
SOURCENM_005962
SOURCENM_130439
SMDHs.602078
SAGEHs.602078
GODNA binding [Amigo]  DNA binding
GOtranscription corepressor activity [Amigo]  transcription corepressor activity
GOnucleus [Amigo]  nucleus
GOnucleus [Amigo]  nucleus
GOregulation of transcription, DNA-dependent [Amigo]  regulation of transcription, DNA-dependent
GOnegative regulation of cell proliferation [Amigo]  negative regulation of cell proliferation
GOtranscription regulator activity [Amigo]  transcription regulator activity
GOcytoplasmic sequestering of transcription factor [Amigo]  cytoplasmic sequestering of transcription factor
GOregulation of transcription [Amigo]  regulation of transcription
PubGeneMXI1
TreeFamMXI1
CTD4601 [Comparative ToxicoGenomics Database]
Other databases
Probes
ProbeMXI1 Related clones (RZPD - Berlin)
PubMed
PubMed30 Pubmed reference(s) in LocusLink

Bibliography

Mxi1, a protein that specifically interacts with Max to bind Myc-Max recognition sites.
Zervos AS, Gyuris J, Brent R
Cell. 1993 ; 72 (2) : 223-232.
PMID 8425219
 
Redefinition of the coding sequence of the MXI1 gene and identification of a polymorphic repeat in the 3' non-coding region that allows the detection of loss of heterozygosity of chromosome 10q25 in glioblastomas.
Albarosa R, DiDonato S, Finocchiaro G
Human genetics. 1995 ; 95 (6) : 709-711.
PMID 7789959
 
Mutation of the MXI1 gene in prostate cancer.
Eagle LR, Yin X, Brothman AR, Williams BJ, Atkin NB, Prochownik EV
Nature genetics. 1995 ; 9 (3) : 249-255.
PMID 7773287
 
Point mutations of the Mxil gene are rare in prostate cancers.
Kawamata N, Park D, Wilczynski S, Yokota J, Koeffler HP
The Prostate. 1996 ; 29 (3) : 191-193.
PMID 8827088
 
Microsatellite instability and deletion analysis of chromosome 10 in human prostate cancer.
Lacombe L, Orlow I, Reuter VE, Fair WR, Dalbagni G, Zhang ZF, Cordon-Cardo C
International journal of cancer. Journal international du cancer. 1996 ; 69 (2) : 110-113.
PMID 8608977
 
Expression, regulation and polymorphism of the mxi1 genes.
Shimizu E, Shirasawa H, Kodama K, Sato T, Simizu B
Gene. 1996 ; 176 (1-2) : 45-48.
PMID 8918230
 
No germline mutations in the dimerization domain of MXI1 in prostate cancer clusters. The CRC/BPG UK Familial Prostate Cancer Study Collaborators. Cancer Research Campaign/British Prostate Group.
Edwards SM, Dearnaley DP, Ardern-Jones A, Hamoudi RA, Easton DF, Ford D, Shearer R, Dowe A, Eeles RA
British journal of cancer. 1997 ; 76 (8) : 992-1000.
PMID 9376279
 
MXI1, a putative tumor suppressor gene, suppresses growth of human glioblastoma cells.
Wechsler DS, Shelly CA, Petroff CA, Dang CV
Cancer research. 1997 ; 57 (21) : 4905-4912.
PMID 9354456
 
Repression by the Mad(Mxi1)-Sin3 complex.
Schreiber-Agus N, DePinho RA
BioEssays : news and reviews in molecular, cellular and developmental biology. 1998 ; 20 (10) : 808-818.
PMID 9819568
 
Expression of MXI1, a Myc antagonist, is regulated by Sp1 and AP2.
Benson LQ, Coon MR, Krueger LM, Han GC, Sarnaik AA, Wechsler DS
The Journal of biological chemistry. 1999 ; 274 (40) : 28794-28802.
PMID 10497252
 
Two MAD tails: what the recent knockouts of Mad1 and Mxi1 tell us about the MYC/MAX/MAD network.
Foley KP, Eisenman RN
Biochimica et biophysica acta. 1999 ; 1423 (3) : M37-M47.
PMID 10382539
 
Mxi1 is a repressor of the c-Myc promoter and reverses activation by USF.
Lee TC, Ziff EB
The Journal of biological chemistry. 1999 ; 274 (2) : 595-606.
PMID 9872993
 
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

Contributor(s)

Written12-1999Niels B Atkin

Citation

This paper should be referenced as such :
Atkin NB . MXI1. Atlas Genet Cytogenet Oncol Haematol. December 1999 .
URL : http://AtlasGeneticsOncology.org/Genes/MXI1ID209.html

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed Jul 2 08:25:16 2008


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

j.l.huret@chu-poitiers.fr.