Roose M L, Schwarzacher T, Heslop-Harrison J S
Department of Cell Biology, John Innes Centre, Norwich, England.
J Hered. 1998 Jan-Feb;89(1):83-6. doi: 10.1093/jhered/89.1.83.
In situ hybridization of 18S-5.8S-25S rDNA probes labeled with biotin or rhodamine and 5S rDNA probes labeled with digoxigenin was used to locate rDNA sites on root-tip metaphase chromosomes of Citrus sinensis L. (2n = 2x = 18), Poncirus trifoliata L. Raf. (2n = 2x = 18), and Citrus x Poncirus hybrids (2n = 2x = 18). Counterstaining with the fluorochromes chromomycin A3 and DAPI uniquely identified many but not all chromosomes. C. sinensis had five 18S-25S rDNA sites, P. trifoliata had seven, and three different Citrus x Poncirus hybrids had five or six sites. Four 5S rDNA sites were detected, mostly linked to 18S-25S rDNA sites. Overall we observed high levels of chromosomal heterozygosity in all accessions examined.
采用生物素或罗丹明标记的18S - 5.8S - 25S rDNA探针以及地高辛标记的5S rDNA探针原位杂交,以定位甜橙(Citrus sinensis L.,2n = 2x = 18)、枳(Poncirus trifoliata L. Raf.,2n = 2x = 18)和柑橘与枳的杂种(2n = 2x = 18)根尖中期染色体上的rDNA位点。用荧光染料色霉素A3和DAPI复染,能独特地识别许多但并非所有染色体。甜橙有5个18S - 25S rDNA位点,枳有7个,3个不同的柑橘与枳杂种有5个或6个位点。检测到4个5S rDNA位点,大多与18S - 25S rDNA位点相连。总体而言,我们在所检测的所有材料中都观察到了高水平的染色体杂合性。