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黑腹果蝇中核糖体DNA插入片段的表达

Expression of ribosomal DNA insertions in Drosophila melanogaster.

作者信息

Long E O, Dawid I B

出版信息

Cell. 1979 Dec;18(4):1185-96. doi: 10.1016/0092-8674(79)90231-9.

Abstract

Approximately half of the ribosomal genes on the X chromosome of Drosophila melanogaster are interrupted by an insertion of type 1. Nuclear RNA from D. melanogaster embryos was transferred to DBM paper and hybridized with cloned type 1 insertion sequences. With a DNA fragment derived specifically from large insertions, transcripts were detected between 5 and 10 kb. These insertion transcripts represent less than one RNA molecule per nucleus, which is more than three orders of magnitude below the concentration of nascent rRNA chains, as determined by kinetics of hybridization. With a DNA fragment derived from the right end of large insertions which is also complementary to short insertions, more discrete RNA bands appeared with sizes between 1 and 8.5 kb, representing altogether about 13 RNA molecules per nucleus. Insertion transcripts large enough to be potential precursors to 28S rRNA represent less than one molecule per nucleus. It was shown by sandwich hybridization that at least some of the insertion transcripts are derived from rDNA. No significant difference was found between insertion transcripts in RNA extracted from ovaries, embryos, larvae, pupae or adult flies. Unless a mechanism other than splicing is involved, ribosomal genes with insertions cannot contribute significantly to the synthesis of 28S rRNA. A cytoplasmic RNA approximately 1 kb long, which is complementary to a short insertion and to ribosomal gene sequences flanking both sides of the insertion, was found. The abundance of this short unspliced RNA is about 50 molecules per embryo cell.

摘要

黑腹果蝇X染色体上大约一半的核糖体基因被1型插入序列打断。将黑腹果蝇胚胎的核RNA转移到DBM纸上,并用克隆的1型插入序列进行杂交。用专门从大插入片段衍生而来的DNA片段,检测到5至10 kb之间的转录本。这些插入转录本每个细胞核中不到一个RNA分子,比通过杂交动力学测定的新生rRNA链浓度低三个数量级以上。用来自大插入片段右端且也与短插入片段互补的DNA片段,出现了更离散的RNA条带,大小在1至8.5 kb之间,每个细胞核总共约有13个RNA分子。大到足以成为28S rRNA潜在前体的插入转录本每个细胞核中不到一个分子。通过夹心杂交表明,至少一些插入转录本源自rDNA。从卵巢、胚胎、幼虫、蛹或成虫中提取的RNA中的插入转录本之间未发现显著差异。除非涉及剪接以外的机制,带有插入序列的核糖体基因对28S rRNA的合成贡献不大。发现了一种约1 kb长的细胞质RNA,它与短插入片段以及插入片段两侧的核糖体基因序列互补。这种短的未剪接RNA的丰度约为每个胚胎细胞50个分子。

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