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Mapping of MAX to human chromosome 14 and mouse chromosome 12 by in situ hybridization.

作者信息

Gilladoga A D, Edelhoff S, Blackwood E M, Eisenman R N, Disteche C M

机构信息

Department of Pathology, School of Medicine, University of Washington, Seattle 98195.

出版信息

Oncogene. 1992 Jun;7(6):1249-51.

PMID:1594250
Abstract

The protein encoded by the MAX gene is a member of the class of basic region-helix-loop-helix-zipper proteins and has been demonstrated to associate with N-, L-, and c-Myc proteins both in vitro and in vivo. Heterodimers formed between c-Myc and Max proteins have been shown to possess sequence-specific DNA-binding activity. Here we report the mapping of the MAX gene to a single region on human chromosome 14 (bands q22-q24) and to mouse chromosome 12 (region D). Chromosome abnormalities linked to several neoplasms have been previously associated with this region on human chromosome 14. The mapping results also confirm a region of homology between human chromosome 14q22-24 and mouse chromosome 12 region D.

摘要

相似文献

1
Mapping of MAX to human chromosome 14 and mouse chromosome 12 by in situ hybridization.
Oncogene. 1992 Jun;7(6):1249-51.
2
Mapping of two genes encoding members of a distinct subfamily of MAX interacting proteins: MAD to human chromosome 2 and mouse chromosome 6, and MXI1 to human chromosome 10 and mouse chromosome 19.两个编码MAX相互作用蛋白不同亚家族成员的基因定位:MAD定位于人类2号染色体和小鼠6号染色体,MXI1定位于人类10号染色体和小鼠19号染色体。
Oncogene. 1994 Feb;9(2):665-8.
3
Assignment of the human MAD and MXI1 genes to chromosomes 2p12-p13 and 10q24-q25.人类MAD和MXI1基因定位于染色体2p12 - p13和10q24 - q25。
Genomics. 1994 Sep 1;23(1):282-5. doi: 10.1006/geno.1994.1496.
4
Low molecular weight inhibitors of Myc-Max interaction and function.Myc-Max相互作用及功能的低分子量抑制剂
Oncogene. 2003 Sep 18;22(40):6151-9. doi: 10.1038/sj.onc.1206641.
5
Evolutionary relationships and functional conservation among vertebrate Max-associated proteins: the zebra fish homolog of Mxi1.脊椎动物Max相关蛋白之间的进化关系和功能保守性:Mxi1的斑马鱼同源物
Oncogene. 1994 Nov;9(11):3167-77.
6
Identification of casein kinase II phosphorylation sites in Max: effects on DNA-binding kinetics of Max homo- and Myc/Max heterodimers.鉴定Max中酪蛋白激酶II的磷酸化位点:对Max同源二聚体和Myc/Max异源二聚体DNA结合动力学的影响。
Oncogene. 1993 Dec;8(12):3211-20.
7
myc, max, and a novel rlf-L-myc fusion protein in small-cell lung cancer.小细胞肺癌中的Myc、Max和一种新型rlf-L-Myc融合蛋白
Princess Takamatsu Symp. 1991;22:307-18.
8
Mmip1: a novel leucine zipper protein that reverses the suppressive effects of Mad family members on c-myc.Mmip1:一种新型亮氨酸拉链蛋白,可逆转Mad家族成员对c-myc的抑制作用。
Oncogene. 1998 Mar 5;16(9):1149-59. doi: 10.1038/sj.onc.1201634.
9
The basic region/helix-loop-helix/leucine zipper domain of Myc proto-oncoproteins: function and regulation.Myc原癌蛋白的碱性区域/螺旋-环-螺旋/亮氨酸拉链结构域:功能与调控
Oncogene. 1999 May 13;18(19):2955-66. doi: 10.1038/sj.onc.1202750.
10
Analysis of the Myc and Max interaction specificity with lambda repressor-HLH domain fusions.Myc与λ阻遏物-HLH结构域融合体相互作用特异性的分析。
J Mol Biol. 1995 May 5;248(3):541-50. doi: 10.1006/jmbi.1995.0241.

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Overexpression of kinase-associated phosphatase (KAP) in breast and prostate cancer and inhibition of the transformed phenotype by antisense KAP expression.激酶相关磷酸酶(KAP)在乳腺癌和前列腺癌中的过表达以及反义KAP表达对转化表型的抑制作用。
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3
A minimal regulatory region maintains constitutive expression of the max gene.
一个最小调控区域维持max基因的组成型表达。
Mol Cell Biol. 1997 Mar;17(3):1037-48. doi: 10.1128/MCB.17.3.1037.
4
The nerve growth factor-responsive PC12 cell line does not express the Myc dimerization partner Max.对神经生长因子有反应的PC12细胞系不表达Myc二聚化伴侣Max。
Mol Cell Biol. 1995 Jul;15(7):3470-8. doi: 10.1128/MCB.15.7.3470.