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18-26S rDNA在4种重楼属植物中的定位
引用本文:王丽,李云飞,唐荣华,顾志建.18-26S rDNA在4种重楼属植物中的定位[J].中国科学院研究生院学报,2004,42(5):419-426.
作者姓名:王丽  李云飞  唐荣华  顾志建
作者单位:四川大学生命科学学院
摘    要:为探讨rDNA在重楼属Paris L.中的分布规律,利用荧光原位杂交(FISH)对4种重楼属植物 的18-26S rDNA进行了定位。所有植物均为二倍体,基因组由A、B、C、D和 E5条染色体构成。(1)滇重楼P.polyphylla var.yunnanensis:2n=10=6m+4t,C和D染色体的 短臂上各有1个18-26S rDNA位点;(2)长柱重楼P.forrestii:2n=10=6m+4t,B染色体的长臂 、C和D染色体的短臂上各有1个位点;(3)五指莲P.axialis:2n=10=6m(2sat)+4t(2sat) +1-2B,C和D染色体的短臂上各有1个位点;在有1个B染色体的细胞中,B染色体没有信号点, 而有2个B染色体的细胞中,只有1个B染色体上有信号点,表明B染色体上有基因存在且其分裂 不均等;(4)大理重楼P.daliensis:2n=10=4m+2sm+2st+2t,C染色体的短臂上有1个位点。1 8-26S rDNA位点不仅出现在染色体的次缢痕上,也出现在非次缢痕位点。另外,4个种中C染 色体短臂末端均有18-26S rDNA。

关 键 词:重楼属  荧光原位杂交  18-26S  rDNA  B染色体

Mapping of18-26S rDNA loci in four species of the genus Paris by fluorescence in situ hybridization(FISH)
WANG Li,LI Yun-Fei,TANG Rong-Hua,GU Zhi-Jian.Mapping of18-26S rDNA loci in four species of the genus Paris by fluorescence in situ hybridization(FISH)[J].Journal of the Graduate School of the Chinese Academy of Sciences,2004,42(5):419-426.
Authors:WANG Li  LI Yun-Fei  TANG Rong-Hua  GU Zhi-Jian
Abstract:18-26S rDNA loci were mapped on chromosomes in four species of Par is,and the num-ber and position of rDNA sites in these species were compared f or analysis of the distribution of the sites. All the plants were diploids,and t he genome consisted of five chromosomes,A,B,C,D and E. (1)P. polyphylla var. yunnanensis,2n=10=6m+4t. Two18-26S rDNA loci were de-tected on the short arms o f C and D chromosomes;(2)P. forrestii,2n=10=6m+4t. One locus was detected on th e long arm of B chromosome,and also two loci on the short arms of C and D chro- mosomes;(3)P. axialis. 2n=10=6m(2sat)+4t(2sat)+1-2B. Two loci were detected o n the short arms of C and D chromosomes. One locus was detected in the cell with t wo B-chromosomes(B),but none was detected in that with only one B chromosome, indicating that rRNA gene existed on B chromsome,and an unequal division occurr ed during mitotic cycle of B-chromosomes. (4)P. daliensis,2n=10=4m+2sm+2st+2t. O ne locus was detected on the short arm of D chromo-some. The signals of18-26S rD NA appeared not only in the second constriction but also in the other regions of chromosome. It is noteworthy that one locus was detected in the terminal region o n the short arm of C chromosome in all the four species studied.
Keywords:Paris  fluorescence in situ hybridization(FISH)  18-26S rDNA  B c
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