Enzyme Maceration, Fluorescent Staining, and FISH of rDNA of Pineapple (Ananas comosus (L.) Merr.) Chromosomes

被引:3
|
作者
Yamamoto, Masashi [1 ]
Takeuchi, Makoto [2 ]
Nashima, Kenji [3 ]
Yamamoto, Toshiya [4 ]
机构
[1] Kagoshima Univ, Fac Agr, Kagoshima 8900065, Japan
[2] Okinawa Prefectural Agr Res Ctr, Nago Branch, Nago 9050012, Japan
[3] Nihon Univ, Coll Bioresource Sci, Fujisawa, Kanagawa 2520880, Japan
[4] NARO, Inst Fruit Tree & Tea Sci, Tsukuba, Ibaraki 3058605, Japan
来源
HORTICULTURE JOURNAL | 2019年 / 88卷 / 04期
关键词
CMA; DAPI; EMA; fluorescence in situ hybridization; ribosomal RNA gene; IN-SITU HYBRIDIZATION; RIBOSOMAL-RNA GENES; 5S; EVOLUTION; GENOME; SPP; CYTOTAXONOMY; KARYOTYPE; VARIETIES; SINENSIS;
D O I
10.2503/hortj.UTD-102
中图分类号
S6 [园艺];
学科分类号
0902 ;
摘要
Chromosome analysis of pineapple (Ananas comosus (L.) Merr.), one of the most important tropical fruit trees, was conducted. All experiments were carried out using root tips derived from three cross combinations as plant materials. Good preparations, with all 50 chromosomes relatively extended and well-spread without cytoplasm, were observed under enzyme conditions of "2% Cellulase Onozuka RS and 0.5% Pectolyase Y-23" without pretreatment with 2 mM 8-hydroxyquinoline. CMA-positive (+) bands were observed in telomeric positions of two chromosomes. DAN-negative bands (-) corresponded with CMA+ bands. The numbers and positions of CMA+ bands were stable. Fluorescence in situ hybridization of rDNA was performed. The 18S-5.8S-25S rDNA sites were detected in telomeric positions of two chromosomes. The 5S rDNA sites were also detected in telomeric positions of two chromosomes. The 5S and 18S-5.8S-25S rDNA sites were located on different chromosomes. The 18S-5.8S-25S rDNA sites corresponded with the CMA+/DAPI- bands. The numbers and positions of rDNA sites were stable.
引用
收藏
页码:455 / 461
页数:7
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