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酿酒酵母核仁中核酸序列的超微结构定位

Ultrastructural localization of nucleic acid sequences in Saccharomyces cerevisiae nucleoli.

作者信息

Dvorkin N, Clark M W, Hamkalo B A

机构信息

Department of Molecular Biology and Biochemistry, University of California, Irvine 92717.

出版信息

Chromosoma. 1991 Sep;100(8):519-23. doi: 10.1007/BF00352202.

Abstract

The putative nucleolus in Saccharomyces cerevisiae is visible in electron micrographs as a darkly stained, crescent-shaped structure associated with the nuclear envelope. The haploid yeast genome contains 100-200 tandem copies of a 9.1 kb ribosomal DNA (rDNA) repeat predicted to reside in this structure. We combined in situ hybridization of non-isotopically labeled probes to isolated S. cerevisiae nuclei with immunogold detection to localize rDNA and rDNA precursor sequences in nuclei at the electron microscope (EM) level. Gold particles are restricted to defined regions of nuclei which appear more electron dense than the bulk of the nucleus and which generally exhibit the crescent shape typical of the structure thought to be the nucleolus. In addition, snR17, the yeast homolog of mammalian U3, a nucleolar-restricted small nuclear RNA (snRNA), was localized to the same electron dense region of the nucleus. These data, in conjunction with published immunofluorescent localizations of nucleolar-associated antigens, provide definitive proof that the dense crescent is the nucleolus. Finally, the technique described is applicable to probing nuclear organization in a genetically manipulable system.

摘要

在电子显微镜下,酿酒酵母中假定的核仁表现为与核膜相关的深色新月形结构。单倍体酵母基因组包含100 - 200个串联重复的9.1 kb核糖体DNA(rDNA),预计位于该结构中。我们将非同位素标记探针与分离的酿酒酵母细胞核进行原位杂交,并结合免疫金检测,在电子显微镜(EM)水平上定位细胞核中的rDNA和rDNA前体序列。金颗粒局限于细胞核的特定区域,这些区域比细胞核的大部分区域电子密度更高,并且通常呈现出被认为是核仁的典型新月形结构。此外,哺乳动物U3的酵母同源物snR17,一种核仁特异性小核RNA(snRNA),也定位于细胞核的同一电子致密区域。这些数据,结合已发表的核仁相关抗原的免疫荧光定位,提供了确凿证据,证明致密新月形结构就是核仁。最后,所描述的技术适用于在可遗传操作的系统中探究细胞核组织。

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