Checklist of the freshwater fishes of Armenia,Azerbaijan and Georgia

We present a critical checklist of freshwater fish species found so far in the countries of Armenia, Azerbaijan and Georgia. In total 119 freshwater fishes are recorded. There are 40, 86 and 96 species currently known for Armenia, Azerbaijan and Georgia respectively. From these 119 species, seven are endemic and seven species are alien. From the alien species, only three (Carassius gibelio, Gambusia holbrooki and Pseudorasbora parva) can be considered as widespread and invasive. There are four species (Gasterosteus aculeatus, Gobio artvinicus, Perca fluviatilis and Salmo gegarkuni) that are translocated within the region. Seven species are confirmed or recorded for the first time including G. artvinicus and Oxynoemacheilus veyselorum for Armenia, Azerbaijan and Georgia, Capoeta kaput and Rhinogobius lindbergi for Azerbaijan and Georgia, Capoeta razii for Azebaijan, Oxynoemacheilus cemali and Squalius agdamicus for Georgia. In this checklist, Acipenser colchicus is treated as a synonym of Acipenser persicus. Sand smelts of the Black and Caspian Sea basin are identified as Atherina caspia and Clupeonella caspia is treated as a synonym of Clupeonella cultriventris. Coregonus sevanicus is listed as Coregonus sp. until the situation of Sevan whitefish is better understood. Capoeta sevangi and Capoeta ekmekciae are synonyms of Capoeta capoeta. The fish often identified as Capoeta capoeta gracilis from rivers south of the Kura most likely belong to C. razii. The Black and Caspian Sea Rutilus populations are treated as conspecific, therefore R. kutum is a junior synonym of R. frisii. Oxynoemacheilus veyseli is valid as O. veyselorum. We list the alien Rhinogobius species as R. lindbergi, however the name is provisional and needs further confirmation. All Squalius species from the Kura River drainage are identified as S. agdamicus, however in the Aras, it is replaced by S. turcicus. Squalius orientalis is treated as a valid species restricted to the eastern Black Sea basin. The four forms of Lake Sevan trout (Salmo ischchan, S. gegarkuni, S. danilewskii and S. aestivalis) are treated as valid species, two of them (S. ischchan and S. danilewskii) are extinct. Rutilus sojuchbulagi from Azerbaijan is also extinct.     

Assignment of two rat dihydrofolate (DHFR) genes to chromosomes 2 and 4

A panel of rat x mouse cell hybrids was used in the chromosomal mapping of the rat dihydrofolate reductase (DHFR) gene. It was determined that the probe hybridized to gene sequences on two different chromosomes (Nos. 2 and 4), possibly representing the active gene and a pseudogene. Hybridization of the DHFR probe to DNA from a methotrexate resistant rat cell line revealed that the gene on chromosome 2 was amplified, but not the gene on chromosome 4. This result was taken to suggest that the active DHFR gene is located on rat chromosome 2 and that the sequence on chromosome 4 is a pseudogene.     

The thyroglobulin gene resides on chromosome 8 in man and on chromosome 7 in the rat

Human chromosomes were separated by a dual laser FACS sorter and their DNA hybridized with a thyroglobulin gene probe. A strong hybridization signal was obtained with DNA from chromosome 8. A panel of mouse-rat cell hybrids was used to determine the chromosomal localization of the rat thyroglobulin gene by the Southern blotting method. Comparison of the cytogenetic data with the hybridization signals obtained with the rat thyroglobulin probe allowed assignment of this gene to rat chromosome 7. It is concluded that the synteny relationship between the thyroglobulin gene and the c-myc oncogene has been conserved in rat and man.     

Characterization of the aldose reductase-encoding gene family in rat.

Although the enzyme aldose reductase (AR) is implicated in the development of tissue pathology in diabetes, the exact mechanism of this involvement remains unclear. To better understand the role that expression of the aldose reductase-encoding gene (ALR) may play in diabetic complications, we have begun to analyze the gene and its regulatory regions, and we present here the sequence of four ALR genes in the rat. The putative functional gene is 14.1 kb long, has ten exons which show perfect sequence identity to the rat lens AR RNA sequence, and nine introns with classical splice-site consensus sequences. Potential regulatory elements in the 5'-flanking region of this gene include a TATA box and two CCAAT boxes. Probing rat genomic Southern blots with a fragment from the first intron indicates that there is probably only one copy of this gene in the rat genome. The other three genes are processed pseudogenes which show approx. 90% identity to the rat lens AR RNA sequence, contain no introns, and have poly(A) regions at their 3' ends. Chromosomal localization studies show the presence of ALR genes on chromosomes 3, 4 and 6 in the rat with the putative functional gene mapped on chromosome 4.