Number Of 5S rDNA Sites Research Articles

A Karyotype Comparison Between Two Closely Related Species of Acrostichum

Acrostichum aureum and A. danaeifolium are morphologically similar sympatric species which grow in mangrove communities. To evaluate the cytological differences between these species, their karyotypes were analyzed with conventional staining, triple-staining with chromomycin A3 (CMA), distamycin A (DA) and DAPI, silver nitrate, and in situ hybridization with 45S rDNA as probe. Both species have the same chromosome number (2n = 60) with only small differences in chromosome size and morphology. The CMA banding pattern revealed four terminal bands in A. danaeifolium and six in A. aureum. DAPI bands were not found. The maximum number of nucleoli per interphase nucleus and the number of 45S rDNA sites were consistent with the number of CMA bands: four in A. danaeifolium and six in A. aureum. All meiotically analyzed materials showed 30II with normal chromosome pairing and segregation, except in one plant with a chromosome bridge and fragment in cells of anaphase I and II. It is suggested that sympatry and karyotypic orthoselection have contributed to keep the morphological and karyological similarities in such widespread species.

Chromosomal location and reorganization of the 45S and 5S rDNA in theBrachyscome lineariloba complex (Asteraceae)

The chromosomal locations of the 45S (18S-5.8S-26S) and 5S ribosomal DNA in theBrachyscome lineariloba complex and two related species have been determined by the use of multicolor fluorescencein situ hybridization (McFISH). TheBrachyscome lineariloba complex includes five cytodemes with 2n=4, 8, 10, 12 and 16. Each of the 5S and 45S rDNA loci occurs at two sites on chromosomes in cytodemes with 2n=4. While in cytodemes with 2n=8, 10, 12 and 16, the number of 5S rDNA sites increases from four to eight paralleled to the genomic addition of diploid (4 chromosomes) or haploid (2 chromosomes) dosage. Of the 5S rDNA sites, only one pair is major, except for the cytodeme with 2n=10. The remaining 5S rDNA sites are minor and seem to have reduced the unit number of the 5S rDNA during the successive genomic additions. The 45S rDNA site is detected only at two nucleolar organizing regions in all cytodemes regardless of successive genomic addition. The loss or diminution of 45S rDNA sequences seem to have proceeded more rapidly than 5S rDNA sequences in theB. lineariloba complex.