Hayashi Akiko, Saito Toshiyuki, Mukai Yasuhiko, Kurita Siro, Hori Tada-aki
Transcriptome Profiling Group, National Institute of Radiological Sciences, Chiba, Japan.
Genes Genet Syst. 2005 Jun;80(3):199-212. doi: 10.1266/ggs.80.199.
The genetic variations of Lycoris radiata var. radiata, a completely sterile triploid from Japan, were examined by comparing the nucleotide sequences of genomic DNA regions in 11 triploid strains sampled from Japan and four triploid strains sampled from China, and in two diploid strains of Lycoris radiata var. pumila, which is endemic to China and fertile. For this purpose, two genes were analyzed, the lectin gene in the nuclear genome and the maturase gene in the chloroplast genome. A clear genetic constancy was observed in their DNA nucleotide sequences. For both genes, completely identical nucleotide sequences were detected in the 11 Japanese and four Chinese triploid strains and also between the two Chinese diploid strains. However, some genetic variations were observed between the Japanese and Chinese triploid strains, and between the triploid and diploid strains. These results are consistent with the findings obtained from previous chromosome karyotype analyses and allozyme analyses. In addition, in our preliminary FISH analysis of the physical mapping of the rRNA gene family, the 18S-5.8S-26S rRNA and 5S rRNA loci were localized on six and four chromosomes, respectively. Regarding the 18S-5.8S-26S rRNA loci, two were associated with two SAT chromosomes. The remaining four were distinguished by having no secondary constriction. Localization of 5S rRNA loci to chromosome spreads revealed three sites on the proximal part of the long arm of three acrocentric chromosomes and one site on the distal part of the long arm of the SAT chromosome; the latter site was juxtaposed to the 18S-5.8S-26S rRNA loci. These findings indicate that L. radiata var. radiata is not a typical autotriploid. The present paper discusses the possible origin of L. radiata var. radiata from a diploid variety of L. radiata var. pumila, based on the molecular cytogenetic analysis and DNA sequence analysis.
对来自日本的完全不育三倍体忽地笑变种的遗传变异进行了研究,通过比较从日本采集的11个三倍体菌株、从中国采集的4个三倍体菌株以及中国特有的可育忽地笑变种的两个二倍体菌株的基因组DNA区域的核苷酸序列来进行检测。为此,分析了两个基因,核基因组中的凝集素基因和叶绿体基因组中的成熟酶基因。在它们的DNA核苷酸序列中观察到明显的遗传稳定性。对于这两个基因,在11个日本三倍体菌株和4个中国三倍体菌株中以及两个中国二倍体菌株之间检测到完全相同的核苷酸序列。然而,在日本和中国的三倍体菌株之间以及三倍体和二倍体菌株之间观察到了一些遗传变异。这些结果与先前染色体核型分析和等位酶分析的结果一致。此外,在我们对rRNA基因家族物理图谱的初步荧光原位杂交分析中,18S - 5.8S - 26S rRNA和5S rRNA基因座分别定位在6条和4条染色体上。关于18S - 5.8S - 26S rRNA基因座,两个与两条随体染色体相关。其余四个的区别在于没有次缢痕。5S rRNA基因座在染色体铺展上的定位显示,在三条近端着丝粒染色体长臂的近端部分有三个位点,在随体染色体长臂的远端部分有一个位点;后一个位点与18S - 5.8S - 26S rRNA基因座相邻。这些发现表明忽地笑变种不是典型的同源三倍体。本文基于分子细胞遗传学分析和DNA序列分析,讨论了忽地笑变种可能起源于忽地笑变种的二倍体品种。