RESTRICTION FRAGMENT LENGTH POLYMORPHISMS(RFLPs) OF THE SMALL-SUBUNIT RIBOSOMAL DNA AS A TOOL FOR IDENTIFICATION OF TILAPIA SPP.

2003 ◽  
Vol 7 (4) ◽  
pp. 465-482 ◽  
Author(s):  
Sabry El-Serafy ◽  
Mohammed Awwad ◽  
Mona Azab ◽  
Nasr-Allah Abd- EI-Hameid
1996 ◽  
Vol 42 (12) ◽  
pp. 1185-1189 ◽  
Author(s):  
Josepa Gené ◽  
Josep Guarro ◽  
José Manuel Guillamón ◽  
Krzysztof Ulfig

In our studies on keratinophilic fungi in Spain, an arthroconidial anamorphic species has been recovered and is herein described as new. Arthrographis alba sp.nov. is characterized by having arthroconidia borne from laterally or pseudodichotomously branched conidiophores, white colonies, and nil or restricted growth at 37 °C. Analysis of restriction fragment length polymorphisms of ribosomal DNA reveals differences with Arthrographis kalrae, a morphologically similar species.Key words: Arthrographis alba, Hyphomycetes, rDNA.


Genome ◽  
1995 ◽  
Vol 38 (3) ◽  
pp. 419-425 ◽  
Author(s):  
Navtej Pal Sappal ◽  
Robert S. Jeng ◽  
Martin Hubbes ◽  
Fuhua Liu

Restriction fragment length polymorphisms from PCR amplified ribosomal DNAs of three Trichogramma species, T. minutum, T. brassicae, and T. near sibiricum, were studied. Length variation in the internal transcribed spacer (ITS) region was observed. The ITS region of T. brassicae is about 1350 base pairs (bp) in length and those of T. minutum and T. near sibiricum are 1300 bp. These three species also differ in the size of their ITS1 and ITS2 regions. Restriction enzyme digestions of these regions showed unique banding patterns for each species. The amplified 18S region of ribosomal DNA is about 1800 bp in length and showed no length variation between the three species of Trichogramma. Restriction enzyme digestion of this region by BamHI differentiated T. brassicae from the other two species. Restriction site maps of the ITS and 18S regions were constructed for each species. The amplified 28S region is about 1700 bp for these three species. Restriction of this region by RsaI and SacII differentiates these three species. The reported results indicate that these species of Trichogramma can be clearly differentiated from one another by nuclear ribosomal DNA markers.Key words: rDNA, Trichogramma, PCR.


1989 ◽  
Vol 35 (12) ◽  
pp. 1146-1155 ◽  
Author(s):  
J. Stephen Horton ◽  
Paul A. Horgen

Within the genus Achyla, which belongs to the class of fungi known as the Oomycetes, taxonomic judgments have traditionally been made using a variety of sexual criteria. We have used restriction fragment length polymorphisms as a new taxonomic character to examine intra- and inter-specific variation within this genus. Using a cDNA clone coding for the Achlya 18S rRNA gene as a hybridization probe, a 10-kb fragment of ribosomal DNA (rDNA) from Achlya ambisexualis strain E87 was cloned and then mapped for selected restriction enzyme sites. In Southern blot hybridizations, both this rDNA fragment and cloned 18S cDNAs revealed differences in the rDNA organization of A. ambisexualis E87 (male) and a female isolate of A. ambisexualis strain 734. No differences in the rDNAs were detected between the two heterothallic isolates A. ambisexualis E87 and A. bisexualis 65-1. Southern blot hybridizations suggested that two different rDNA organizations may exist within the genome of the homothallic strain A. heterosexualis B14. cDNA clones coding for two different hormonally regulated genes revealed the same relationships between the four isolates studied as those determined with rDNA probes. Two homothallic Achlya strains recently isolated from nature were found to have additional DNA polymorphisms not detected in the laboratory strains. Phenetic analysis distinguished the same similarities that were evident upon inspection of the hybridization data. Taken together, these data suggest different relationships between the isolates examined than do the previous taxonomic criteria by which species have been delimited within this genus.Key words: Achlya; restriction fragment length polymorphisms; ribosomal DNA; taxonomy.


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