Hipkins V D, Marshall K A, Neale D B, Rottmann W H, Strauss S H
National Forest Genetic Electrophoresis Laboratory, USDA Forest Service, Camino, CA 95709, USA.
Curr Genet. 1995 May;27(6):572-9. doi: 10.1007/BF00314450.
We determined the DNA sequence of a 2.7-kb cpDNA XbaI fragment from douglas-fir [Pseudotsuga menziesii (Mirb.) Franco]. RFLPs revealed by the 2.7-kb XbaI clone were observed to vary up to 1 kb among species within the genus Pseudotsuga and up to 200 bp among trees of P. menziesii. The polymerase chain reaction (PCR) allowed the locus of polymorphism to be identified, and the variable region was then sequenced in a second Douglas-fir tree, a single tree of a related species, Japanese Douglas-fir (P. japonica), and in a species lacking a mutation hotspot in the region, Pinus radiata (Monterey pine). The locus of polymorphism is characterized by hundreds of base pairs of imperfect, tandem direct repeats flanked by a partially duplicated and an intact trn Y-GUA gene. The duplication is direct in orientation and consists of 43 bp of the 3' end of trnY and 25 bp of its 3' flanking sequence. Tandem repeats show high sequence similarity to a 27-bp region of the trnY gene that overlaps one end of the duplication. The two trees of Douglas-fir sequenced differed by a single tandem repeat unit, whereas these trees differed from the Japanese Douglas-fir sequenced by approximately 34 repeat units. Repetitive DNA in the Pseudotsuga cpDNA hotspot was most likely generated at the time of the partial trnY gene duplication and these sequences expanded by slipped-strand mispairing and unequal crossing-over.
我们测定了花旗松[北美黄杉(Pseudotsuga menziesii (Mirb.) Franco)]叶绿体DNA(cpDNA)上一个2.7kb的XbaI片段的DNA序列。观察发现,该2.7kb XbaI克隆所揭示的限制性片段长度多态性(RFLP)在黄杉属内的物种间差异可达1kb,在北美黄杉的不同植株间差异可达200bp。聚合酶链反应(PCR)能够确定多态性位点,随后对另一株花旗松、一个近缘物种日本花旗松(P. japonica)的单株以及该区域缺乏突变热点的辐射松(Pinus radiata,蒙特里松)中的可变区进行了测序。多态性位点的特征是数百个碱基对的不完美串联直接重复序列,两侧分别是部分重复的和完整的trnY - GUA基因。重复序列的方向是正向的,由trnY基因3'端的43bp及其3'侧翼序列的25bp组成。串联重复序列与trnY基因的一个27bp区域具有高度序列相似性,该区域与重复序列的一端重叠。测序的两株花旗松仅相差一个串联重复单元,而这两株花旗松与测序的日本花旗松相差约34个重复单元。黄杉cpDNA热点区域的重复DNA很可能是在trnY基因部分重复时产生的,这些序列通过滑链错配和不等交换得以扩增。