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本文引用的文献

1
Transactivation-defective c-MycS retains the ability to regulate proliferation and apoptosis.转录激活缺陷型c-MycS保留调节增殖和凋亡的能力。
Genes Dev. 1998 Dec 15;12(24):3803-8. doi: 10.1101/gad.12.24.3803.
2
Phenotypes of c-Myc-deficient rat fibroblasts isolated by targeted homologous recombination.通过靶向同源重组分离的c-Myc缺陷型大鼠成纤维细胞的表型。
Cell Growth Differ. 1997 Oct;8(10):1039-48.
3
Identification of putative c-Myc-responsive genes: characterization of rcl, a novel growth-related gene.推定的c-Myc反应基因的鉴定:新型生长相关基因rcl的特性分析
Mol Cell Biol. 1997 Sep;17(9):4967-78. doi: 10.1128/MCB.17.9.4967.
4
c-Myc transactivation of LDH-A: implications for tumor metabolism and growth.乳酸脱氢酶A的c-Myc反式激活:对肿瘤代谢和生长的影响
Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):6658-63. doi: 10.1073/pnas.94.13.6658.
5
Myc represses the growth arrest gene gadd45.Myc抑制生长停滞基因gadd45。
Oncogene. 1997 Jun 12;14(23):2825-34. doi: 10.1038/sj.onc.1201138.
6
c-myc activates RCC1 gene expression through E-box elements.c-myc通过E-box元件激活RCC1基因的表达。
Oncogene. 1997 May 15;14(19):2301-11. doi: 10.1038/sj.onc.1201067.
7
Myc versus USF: discrimination at the cad gene is determined by core promoter elements.Myc与USF:cad基因处的区分由核心启动子元件决定。
Mol Cell Biol. 1997 May;17(5):2529-37. doi: 10.1128/MCB.17.5.2529.
8
Mnt, a novel Max-interacting protein is coexpressed with Myc in proliferating cells and mediates repression at Myc binding sites.Mnt是一种新型的与Max相互作用的蛋白,在增殖细胞中与Myc共同表达,并介导对Myc结合位点的抑制作用。
Genes Dev. 1997 Jan 1;11(1):44-58. doi: 10.1101/gad.11.1.44.
9
The Myc negative autoregulation mechanism requires Myc-Max association and involves the c-myc P2 minimal promoter.Myc负向自调控机制需要Myc与Max结合,并涉及c-myc P2最小启动子。
Mol Cell Biol. 1997 Jan;17(1):100-14. doi: 10.1128/MCB.17.1.100.
10
Myc-Max heterodimers activate a DEAD box gene and interact with multiple E box-related sites in vivo.Myc-Max异源二聚体激活一个DEAD盒基因,并在体内与多个E盒相关位点相互作用。
EMBO J. 1996 Aug 15;15(16):4344-57.

c-myc基因缺失的细胞会错误调节cad和gadd45,但不会错误调节其他推测的c-Myc靶标。

c-myc null cells misregulate cad and gadd45 but not other proposed c-Myc targets.

作者信息

Bush A, Mateyak M, Dugan K, Obaya A, Adachi S, Sedivy J, Cole M

机构信息

Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544 USA.

出版信息

Genes Dev. 1998 Dec 15;12(24):3797-802. doi: 10.1101/gad.12.24.3797.

DOI:10.1101/gad.12.24.3797
PMID:9869632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC317273/
Abstract

We report here that the expression of virtually all proposed c-Myc target genes is unchanged in cells containing a homozygous null deletion of c-myc. Two noteworthy exceptions are the gene cad, which has reduced log phase expression and serum induction in c-myc null cells, and the growth arrest gene gadd45, which is derepressed by c-myc knockout. Thus, cad and gadd45 are the only proposed targets of c-Myc that may contribute to the dramatic slow growth phenotype of c-myc null cells. Our results demonstrate that a loss-of-function approach is critical for the evaluation of potential c-Myc target genes.

摘要

我们在此报告,在含有c-myc纯合无效缺失的细胞中,几乎所有提出的c-Myc靶基因的表达均未改变。两个值得注意的例外是基因cad,其在c-myc缺失细胞中的对数期表达和血清诱导降低,以及生长停滞基因gadd45,其在c-myc基因敲除后被解除抑制。因此,cad和gadd45是c-Myc唯一可能导致c-myc缺失细胞显著生长缓慢表型的靶基因。我们的结果表明,功能丧失方法对于评估潜在的c-Myc靶基因至关重要。