Chromosome numbers for three species of medicinal leeches (Hirudo spp.).

Karyological preparations were made from the testisacs of three medicinal leech species Hirudo medicinalis Linnaeus, 1758, H. verbana Carena, 1820 and H. orientalis Utevsky & Trontelj, 2005 .

The medicinal leech as a convenient tool for water toxicity assessment.

Medicinal leeches previously were used in various toxicological and pharmacological studies because they are sensitive and easy to keep under laboratory conditions. Toxicological studies using leeches became restricted when their natural sources decreased dramatically. We breed medicinal leeches under laboratory conditions and have the possibility of using them for various investigations.

Water and sediment toxicity assessment by use of behavioural responses of medicinal leeches.

Behaviour has been shown to be a sensitive indicator of chemically induced stress and pathology in aquatic organisms. However, ecotoxicological investigations on medicinal leech are restricted because of scarce leech resources in natural waters. We used artificially bred medicinal leech (Hirudo medicinalis L.

Synthesis and physical characterization of DNA fragments containing N4-methylcytosine and 5-methylcytosine.

The synthesis of N4-methyl-2'-deoxycytidine and its fully protected mononucleotide, suitable for the oligonucleotide synthesis by phosphotriester method is described. A set of octanucleotides - d(CGCGCGCG), d(CG5mCGCGCG), d(CG4mCGCGCG) and dodecanucleotides - d(GGACCCGGGTCC), d(GGA5mCCCGGGTCC), d(GGA4mCCCGGGTCC) has been synthesized in a solution. Physical characterization of the oligonucleotide duplexes by means of UV and CD spectrometry provides the evidence that 4mC similarly to 5mC favours the B--greater than Z transition, although both of these methylated cytosines inhibit the B--greater than A conformational change.

Cleavage of methylated CCCGGG sequences containing either N4-methylcytosine or 5-methylcytosine with MspI, HpaII, SmaI, XmaI and Cfr9I restriction endonucleases.

The cleavage specificity of R.Cfr9I was determined to be C decreases CCGGG whereas the methylation specificity of M.Cfr9I was C4mCCGGG.