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构巢曲霉5-氮杂胞苷敏感型fluF基因座的发育特征及染色体定位

Developmental characterization and chromosomal mapping of the 5-azacytidine-sensitive fluF locus of Aspergillus nidulans.

作者信息

Tamame M, Antequera F, Santos E

机构信息

Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.

出版信息

Mol Cell Biol. 1988 Aug;8(8):3043-50. doi: 10.1128/mcb.8.8.3043-3050.1988.

Abstract

In Aspergillus nidulans, a fungus that possesses negligible, if any, levels of methylation in its genome, low concentrations of 5-azacytidine (5-AC) convert a high percentage of the cell population to fluffy phenotypic variants through a heritable modification of a single nuclear gene (M. Tamame, F. Antequera, J. R. Villanueva, and T. Santos, Mol. Cell. Biol. 3:2287-2297, 1983). This new 5-AC-altered locus, designated here fluF1, was mapped as the closest marker to the centromere that has been identified so far on the right arm of chromosome VIII. Of all mutagens tested, only 5-AC induced the fluffy phenotype with a significant frequency. Furthermore, we determined that the wild-type, dominant allele of the fluF gene was primarily accessible to modification by 5-AC at the initial stages of fungal vegetative growth. These results indicated that 5-AC does not act through random mutagenic action but, rather, that fluF constitutes a specific target for this drug during a well-defined period of fungal development. Alteration of fluF by 5-AC resulted in a dramatic modification of the developmental program of A. nidulans. The resulting fluffy clones were characterized by massive, uncontrolled proliferation of undifferentiated hyphae, a drastic delay in the onset of asexual differentiation (conidiation), and colonies with an invasive nature. These features are reminiscent of the malignant properties of tumor cells. We propose that the locus fluF plays a primary role in the control of cell proliferation in A. nidulans and that its alteration by 5-AC produces pleiotropic modifications of the developmental program of this fungus.

摘要

在构巢曲霉中,这种真菌基因组中的甲基化水平即便有也微乎其微,低浓度的5-氮杂胞苷(5-AC)通过对单个核基因的可遗传修饰,将高比例的细胞群体转化为蓬松表型变体(M. 塔马梅、F. 安特克拉、J. R. 比利亚努埃瓦和T. 桑托斯,《分子细胞生物学》3:2287 - 2297,1983年)。这个新的5-AC改变的位点,在此处命名为fluF1,被定位为到目前为止在第八条染色体右臂上已鉴定出的最靠近着丝粒的标记。在所有测试的诱变剂中,只有5-AC能以显著频率诱导出蓬松表型。此外,我们确定fluF基因的野生型显性等位基因在真菌营养生长的初始阶段主要易于被5-AC修饰。这些结果表明5-AC并非通过随机诱变作用起作用,而是fluF在真菌发育的特定明确时期构成了这种药物的一个特定靶点。5-AC对fluF的改变导致构巢曲霉发育程序的显著改变。产生的蓬松克隆的特征是未分化菌丝大量、不受控制地增殖,无性分化(产孢)开始显著延迟,以及菌落具有侵袭性。这些特征让人联想到肿瘤细胞具有的恶性特性。我们提出fluF位点在构巢曲霉细胞增殖控制中起主要作用,并且其被5-AC改变会对这种真菌的发育程序产生多效性修饰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab9/363530/ececcd9989fc/molcellb00068-0069-a.jpg

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