Biology Department, Brookhaven National Laboratory, 11973, Upton, NY, U.S.A..
Plant Mol Biol. 1985 Nov;5(6):353-61. doi: 10.1007/BF00037556.
Restriction endonuclease digestion and Southern blotting procedure were used to determine differences between extrachromosomal, nuclear, plastid, and mitochondrial DNAs from meristematic cells of cultured pea roots.Extrachromosomal and nuclear DNA are highly methylated and neither DNA is homologous to plastid or mitochondrial DNA. Hybridization of extrachromosomal DNA to nuclear DNA indicated that extrachromosomal DNA differed quantitatively from total nuclear DNA in repetitive sequences. Cloned rDNA showed that extrachromosomal DNA contains rRNA genes but the hybridization signal indicated that the copy number was less than that expected if the molecules were amplified. These and cytological findings suggest that extrachromosomal DNA is involved in or a product of genomic changes associated with the onset of differentiation by precursor cells of vascular parenchyma and the root cap.
通过限制内切酶消化和 Southern 印迹程序,从培养豌豆根分生细胞的染色体外、核、质体和线粒体 DNA 中确定差异。染色体外和核 DNA 高度甲基化,并且没有 DNA 与质体或线粒体 DNA 同源。染色体外 DNA 与核 DNA 的杂交表明,染色体外 DNA 在重复序列方面与总核 DNA 在数量上存在差异。克隆的 rDNA 表明染色体外 DNA 含有 rRNA 基因,但杂交信号表明,如果分子被扩增,其拷贝数低于预期。这些和细胞学发现表明,染色体外 DNA 参与或产生与维管束薄壁细胞和根冠前体细胞分化相关的基因组变化。