Phillips J P
Biochem Genet. 1979 Feb;17(1-2):97-104. doi: 10.1007/BF00484476.
The in vitro incorporation of gamma-32P-labeled nucleoside triphosphates into RNA by Drosophila melanogaster form II RNA polymerase from template sites which afford protection from the initiation inhibitor, polyriboinosinic acid (poly [I]), is used as a method for enumerating a specific class of transcription initiation sites on D. melanogaster DNA. Such sites number about 4000 per haploid genome for D. melanogaster. This value is in good agreement with the number of functional genetic units in the D. melanogaster genome as determined by classical cytogenetics.
利用果蝇II型RNA聚合酶将γ-32P标记的核苷三磷酸体外掺入RNA,该掺入过程发生在能免受起始抑制剂多聚肌苷酸(poly [I])影响的模板位点上,以此作为一种方法来计数果蝇DNA上特定类别的转录起始位点。对于果蝇来说,每个单倍体基因组中这类位点的数量约为4000个。这个数值与通过经典细胞遗传学确定的果蝇基因组中功能基因单位的数量高度一致。