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Localization of tandemly repeated DMA sequences in Arabidopsis thaliana
Author(s) -
Maluszynska J.,
HeslopHarrison J.S.
Publication year - 1991
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1111/j.1365-313x.1991.00159.x
Subject(s) - biology , centromere , ploidy , interphase , in situ hybridization , fluorescence in situ hybridization , heterochromatin , cytogenetics , chromosome , microbiology and biotechnology , karyotype , nucleolus , aneuploidy , molecular cytogenetics , genetics , gene , gene expression , cytoplasm
Summary In‐situ hybridization to interphase nuclei and chromosomes of Arabidopsis thaliana (2n = 10) shows that there are four sites of rDNA in a diploid nucleus. The sites are located on chromosomes 2 and 4, and the strength of hybridization indicates that copy number is similar at both pairs of sites. Hybridization to trisomic line 4 revealed five hybridization sites. Silver staining of nucleoli demonstrates that all four loci can be active in diploid interphase nuclei. The tandemly repeated probe pAL1 hybridizes near to the centromeres of all five chromosome pairs. In diploid interphase nuclei, 10 sites of hybridization are detected, while 15 are seen in triploid nuclei. The sites of hybridization co‐localize with the centromeric heterochromatin visualized by staining DNA with the fluorochrome DAPI. The results demonstrate that molecular cytogenetics can be applied to A. thaliana and high resolution physical chromosome maps can be generated. Both probes may be useful for interphase cytogenetics, where they enable chromosome number and aneuploidy to be examined in tissues without divisions. The physical localization of these hybridization sites provides a starting point for linking RFLP and physical chromosome maps.