首页> 美国卫生研究院文献>Nucleic Acids Research >Organization of highly repetitive satellite DNA of two Cucurbitaceae species (Cucumis melo and Cucumis sativus).
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Organization of highly repetitive satellite DNA of two Cucurbitaceae species (Cucumis melo and Cucumis sativus).

机译:两种葫芦科物种(Cucumis melo和Cucumis sativus)的高度重复性卫星DNA的组织。

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摘要

The prominent satellites of the Cucurbitaceae Cucumis melo (melon) and Cucumis sativus (cucumber) have been characterized, in actinomycin/CsCl gradients where the satellite sequences can be separated from ribosomal, organelle, and main band DNA the location of the satellites is different indicating a different GC content. The purified satellite of C. melo is cut by HindIII into a repeat unit of 380 bp; AluI digestion gives rise to two bands (about 80 and 220 bp in size). The HindIII repeat unit if cloned into pBR325 exhibits new recognition sites for HpaII leaving two bands with 150 and 80 bp suggesting methylation of the C/CGG cutting site in the uncloned material. The restriction pattern indicates an internal sequence repeat within the 380 bp HindIII fragment. The C. sativus satellite is cut by AluI to a repeat unit of 180 bp showing no other recognition site for the restriction enzymes tested so far. About 10% sequence homology has been determined between the C. melo and C. sativus satellites by cross hybridization studies. A high methylation degree of cytosines has been measured for both satellites and the ribosomal DNA of C. sativus (about 30%). No transcription products of the C. melo satellite were found during seedling development.
机译:葫芦科瓜(瓜)和黄瓜(Cucumis sativus)(黄瓜)的突出卫星已经被表征,在放线菌素/ CsCl梯度中,卫星序列可以与核糖体,细胞器和主带DNA分开,卫星的位置不同,这表明不同的GC内容。纯化的C. melo卫星被HindIII切割成380 bp的重复单元。 AluI消化产生两个条带(大小分别约为80和220 bp)。如果将HindIII重复单元克隆到pBR325中,则会显示出对HpaII的新识别位点,留下两条分别为150和80 bp的条带,表明未克隆材料中C / CGG切割位点的甲基化。限制性酶切图谱表明在380 bp HindIII片段内的内部序列重复。 AluI将无花果小卫星切成180 bp的重复单元,显示到目前为止,没有其他限制酶的识别位点。通过交叉杂交研究已经确定了C. melo和C. sativus卫星之间约10%的序列同源性。对于卫星和栽培梭状芽胞杆菌的核糖体DNA,都测量到了胞嘧啶的高甲基化程度(约30%)。在幼苗发育过程中未发现旋毛虫卫星的转录产物。

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