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A Guide to the Russian Academy of Sciences - University of Texas ...

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1997 update: FUNCTIONAL MORPHOLOGY OF CHROMOSOMES<br />

Head Alexander V. Zelenin, M.D., Ph.D., D.Sc., Pr<strong>of</strong>essor<br />

In 1995 <strong>the</strong> research in <strong>the</strong> Labora<strong>to</strong>ry proceeded in <strong>the</strong> following directions: 1. Studying<br />

<strong>the</strong> cell proliferation mechanisms. 2. The transfer <strong>of</strong> foreign genes in<strong>to</strong> plant and<br />

animal cells and investigation <strong>of</strong> transgenic cells and organisms. 3. Studying <strong>the</strong><br />

cereal plant chromosomes and chromosomal analysis <strong>of</strong> <strong>the</strong>se plants. 4. The study<br />

<strong>of</strong> human chromosomes in <strong>the</strong> framework <strong>of</strong> <strong>the</strong> <strong>Russian</strong> National Human Genome<br />

Program. The following basic results were obtained: It has been shown on mouse<br />

cell cultures that <strong>the</strong> reverse transcriptase inhibi<strong>to</strong>rs azidothymidine and carbovir<br />

impair <strong>the</strong> function <strong>of</strong> telomerase, <strong>the</strong> enzyme responsible for maintenance <strong>of</strong><br />

telomeres. These experimental data provide new opportunities for elucidation <strong>of</strong> <strong>the</strong><br />

cell senescence mechanisms. The study <strong>of</strong> karyotype formation in <strong>the</strong> interspecies<br />

and intervariety hybrids <strong>of</strong> cereals continued. The chromosome polymorphism <strong>of</strong><br />

wild Egylops wheat species was investigated using <strong>the</strong> differential C-banding and<br />

fluorescent DNA hybridization in situ. A method for C-like banding <strong>of</strong> barley<br />

chromosomes was developed. This method opens new possibilities for<br />

investigation <strong>of</strong> this cereal genome. We also continued <strong>the</strong> work on localization <strong>of</strong> a<br />

number <strong>of</strong> cosmids, YAC and NotI clones on human chromosomes 3 and 13 using<br />

<strong>the</strong> fluorescent hybridization in situ (FISH). The results obtained were used for<br />

physical mapping <strong>of</strong> <strong>the</strong>se chromosomes in <strong>the</strong> framework <strong>of</strong> <strong>the</strong> respective projects<br />

<strong>of</strong> <strong>the</strong> <strong>Russian</strong> National Human Genome Program. A contigue overlapping an area<br />

<strong>of</strong> <strong>the</strong> chromosome 13 partially lost in B-cell chronic leucosis was created. Tissue<br />

specific expression <strong>of</strong> <strong>the</strong> estS gene was demonstrated for transgenic drosophilae.<br />

The development <strong>of</strong> new devices for <strong>the</strong> analysis <strong>of</strong> hybridization kinetics <strong>of</strong><br />

fluorescently labelled DNA using oligonucleotides immobilized on microchips<br />

continued. This project combines <strong>the</strong> efforts <strong>of</strong> several labora<strong>to</strong>ries <strong>of</strong> <strong>the</strong> Institute<br />

interested in developing <strong>of</strong> a new method for DNA sequencing and molecular<br />

diagnostics.<br />

(9.) The Genome Mobility Labora<strong>to</strong>ry under Iurii V. Il’in, D. Chem S., who<br />

graduated from <strong>the</strong> Moscow State <strong>University</strong> Chemistry Department in 1966, and<br />

defended his <strong>the</strong>sis on <strong>the</strong> study <strong>of</strong> <strong>the</strong> structure <strong>of</strong> <strong>the</strong> chromatine<br />

deoxynucleoproteids in 1970, and defended his dissertation on <strong>the</strong> mobile elements<br />

<strong>of</strong> <strong>the</strong> Drosophila in 1981. He joined <strong>the</strong> institute in 1966. His scientific interests at<br />

present are on genome organization, mobile genetic elements, and <strong>the</strong> control <strong>of</strong><br />

gene expression.<br />

1997 update: GENOME MOBILITY<br />

Head Pr<strong>of</strong>essor Yurii V. Ilyin, Ph.D., D.Sc., Member <strong>of</strong> <strong>the</strong> <strong>Russian</strong> <strong>Academy</strong> <strong>of</strong><br />

<strong>Sciences</strong><br />

The functional role <strong>of</strong> D.melanogaster retrotransposon gypsy virus-like particles as an<br />

infectious fac<strong>to</strong>r was revealed. The gypsy ability <strong>to</strong> invade D. hydei cultured cells<br />

was shown. An unusually long-term stability <strong>of</strong> extrachromosomal gypsy plasmid<br />

constructs in transformed D. hydei cells was demonstrated. These results may be<br />

applied in <strong>the</strong> experiments on gene expression in <strong>the</strong> systems using such vec<strong>to</strong>rs. A<br />

complete nucleotide sequence <strong>of</strong> <strong>the</strong> full-length copy <strong>of</strong> D. melanogaster<br />

retrotransposon mdg3 was determined. It has been shown that this element belongs<br />

<strong>to</strong> <strong>the</strong> gypsy group. It contains one ORF, which includes <strong>the</strong> protease, reverse<br />

transcriptase, RNAse H and integrase domains. The structure <strong>of</strong> a short variant <strong>of</strong><br />

mdg3 was also identified. Such elements have a deletion <strong>of</strong> <strong>the</strong> retrotransposon<br />

internal part and completely lack <strong>the</strong> reverse transcriptase and partly <strong>the</strong> RNAse H<br />

510

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