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DIVERSITY OF PLASTID DNA CONFIGURATION AMONG CLASSES OF EUKARYOTE ALGAE 1
Author(s) -
Coleman Annette W.
Publication year - 1985
Publication title -
journal of phycology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.85
H-Index - 127
eISSN - 1529-8817
pISSN - 0022-3646
DOI - 10.1111/j.0022-3646.1985.00001.x
Subject(s) - plastid , biology , nucleoid , botany , algae , eukaryote , dapi , staining , chloroplast , genome , genetics , escherichia coli , gene
Information is presented concerning the overall arrangement of plastid DNA (ptDNA) in plastids of approximately 100 spp. of eukaryote algae, representing all classes. The three‐dimensional arrangement of the ptDNA was assessed by study of both living and fixed material, stained with the DNA fluorochrome 4′,6‐diamidino‐2‐phenylindole (DAPI), using both phase and fluorescence microscopy. The widespread occurrence of two major types of ptDNA configuration known from prior electron microscopy studies was confirmed. These are (1) DNA densities (nucleoids) of variable size and morphology, scattered throughout the plastid, and (2) a ring nucleoid, beaded or unbeaded, lying just within the girdle lamella. Type 1 is characteristic of Rhodophyta, Dinophyta, Chlorophyta, Cryptophyta, Prymnesiophyceae and Eustigmatophyceae (with one exception). Type 2 is characteristic of Phaeophyceae, Bacillariophyceae, Raphidophyceae, Chrysophyceae (except silicoflagellates and organisms such as Synura and Dinobryon), and Xanthophyceae (with the exception of Vaucheria and three genera known to lack girdle lamellae, Bumilleria, Bumilleriopsis, and Pseudobumilleriopsis). Some of these exceptional forms, as well as Euglenophyta, have configurations of ptDNA not previously recognized. In all the configurations observed, the DNA of a single plastid could be interpreted as being in continuity. This character of plastids appears to be stable under varied conditions of growth and at differing stages of the life cycle, where examined, and has confirmed the reclassification made on other grounds of several taxonomic entities. It has also revealed new questionable classifications. Since DAPI staining is far simpler than serial sectioning for electron microscopy in revealing ptDNA architecture, use of the technique may be valuable for future studies of numerous organisms, both to help in their identification and as an aid to unravelling major taxonomic affinities. In light of the endosymbiont hypothesis, plastid characters may require as great attention as those of the remainder of the cell.