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大鼠5S rDNA间隔序列及该基因在19号染色体极端末端区域的染色体定位。

Rat 5S rDNA spacer sequences and chromosomal assignment of the genes to the extreme terminal region of chromosome 19.

作者信息

Suzuki H, Sakurai S, Matsuda Y

机构信息

Division of Molecular Genetics, Jikei University School of Medicine, Tokyo, Japan.

出版信息

Cytogenet Cell Genet. 1996;72(1):1-4. doi: 10.1159/000134149.

Abstract

Fragments of the spacer region of genes for rat 5S ribosomal RNA (rDNA), which are tandemly repeated, were amplified by PCR with primers specific to the two ends of the coding region for 5S rRNA. Two amplified fragments of approximately 1.6 kb were subcloned and sequenced. The spacer sequences showed a high degree of sequence identity to each other (99.2%) but substantial divergence from those of analogous mouse clones. The homologous regions in the mouse clones were interrupted by the duplication or deletion of small segments of DNA. A 12-mer, 5'-GGCTCTTGGGGC-3', thought to be responsible for efficient transcription, was located from position -33 to position -22 in the rat -5S clones. The genes were mapped by fluorescence in situ hybridization with cloned fragments of rat 5S rDNA as probe. The genes were localized exclusively in a single telomeric region of chromosome 19.

摘要

大鼠5S核糖体RNA(rDNA)基因间隔区的片段是串联重复的,用针对5S rRNA编码区两端的特异性引物通过聚合酶链反应(PCR)进行扩增。两个约1.6 kb的扩增片段被亚克隆并测序。间隔序列彼此间显示出高度的序列同一性(99.2%),但与类似的小鼠克隆的间隔序列有很大差异。小鼠克隆中的同源区域被小段DNA的重复或缺失打断。一个被认为对有效转录起作用的12聚体(5'-GGCTCTTGGGGC-3')位于大鼠5S克隆中从-33位到-22位的位置。用大鼠5S rDNA的克隆片段作为探针,通过荧光原位杂交对这些基因进行定位。这些基因仅定位在19号染色体的一个端粒区域。

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