Thümmler F, Beetz A, Rüdiger W
Botanisches Institut, Universität München, FRG.
FEBS Lett. 1990 Nov 26;275(1-2):125-9. doi: 10.1016/0014-5793(90)81455-w.
The polymerase chain reaction was carried out with primers hybridizing to conserved regions of the phytochrome genes. With DNA from the moss Ceratodon purpureus 5 overlapping fragments were obtained resulting in a continuous nucleotide sequence of 1474 bp. The deduced amino acid sequence showed homology of around 60% with all known phytochrome sequences. The sequences contained a conserved chromophore attachment site. In light-grown Ceratodon protonemata the phytochrome mRNA with the size of about 4.5 kb was detected.
采用与植物色素基因保守区域杂交的引物进行聚合酶链反应。以来自紫萼藓的DNA获得了5个重叠片段,从而得到了一个1474 bp的连续核苷酸序列。推导的氨基酸序列与所有已知的植物色素序列显示出约60%的同源性。这些序列包含一个保守的生色团附着位点。在光照生长的紫萼藓原丝体中检测到了大小约为4.5 kb的植物色素mRNA。