[Suppression of telomerase activity leukemic cells by mutant forms of Rhodospirillum rubrum L-asparaginase]

Biomed Khim. 2017 Jan;63(1):62-74. doi: 10.18097/PBMC2017630162.
[Article in Russian]

Abstract

The active and stable mutant forms of short chain cytoplasmic L-asparaginase type I of Rhodospirillum rubrum (RrA): RrA+N17, D60K, F61L, RrA+N17, A64V, E67K, RrA+N17, E149R, V150P, RrAE149R, V150P and RrAE149R, V150P, F151T were obtained by the method of site-directed mutagenesis. It is established that variants RrA-N17, E149R, V150P, F151T and RrАE149R, V150P are capable to reduce an expression hTERT subunit of telomerase and, hence, activity of telomeres in Jurkat cells, but not in cellular lysates. During too time, L-asparaginases of Escherichia coli, Erwinia carotovora and Wolinella succinogenes, mutant forms RrА+N17, D60K, F61L and RrА+N17, A64V, E67K do not suppress of telomerase activity. The assumption of existence in structure RrA of areas (amino acids residues in the position 146-164, 1-17, 60-67) which are responsible for suppression of telomerase activity is made. The received results show that antineoplastic activity of some variants RrA is connected both with reduction of concentration of free L-asparagine, and with expression suppression of hTERT telomerase subunit, that opens new prospects for antineoplastic therapy.

Metodom saĭt-napravlennogo mutageneza polucheny v ochishchennom sostoianii aktivnye i stabil'nye mutantnye formy korotkotsepochechnoĭ tsitoplazmaticheskoĭ L-asparaginazy I tipa iz Rhodospirillum rubrum (RrA): RrA+N17, D60K, F61L, RrA+N17, A64V, E67K, RrA+N17, E149R, V150P, RrAE149R, V150P i RrAE149R, V150P, F151T. Ustanovleno, chto varianty RrAE149R, V150P, F151T i RrA+N17, E149R, V150P sposobny snizhat' ékspressiiu hTERT sub"edinitsy telomerazy i, sledovatel'no, aktivnost' telomerazy v kletkakh Jurkat, no ne v kletochnykh lizatakh. V to zhe vremia, L-asparaginazy Escherichia coli, Erwinia carotovora, Wolinella succinogenes, mutantnye formy RrA+N17, D60K, F61L i RrA+N17, A64V, E67K ne podavliali aktivnost' telomerazy. Sdelano predpolozhenie o sushchestvovanii v strukture RrA oblasteĭ (aminokislotnye ostatki 146-164, 1-17, 60-67), otvechaiushchikh za podavlenie telomeraznoĭ aktivnosti. Poluchennye rezul'taty pokazyvaiut, chto protivoopukholevaia aktivnost' nekotorykh variantov RrA sviazana kak s umen'sheniem kontsentratsii svobodnogo L-asparagina, tak i s ugneteniem ékspressii hTERT sub"edinitsy telomerazy, chto otkryvaet novye perspektivy dlia protivoopukholevoĭ terapii.

Keywords: L-asparaginase Rhodospirillum rubrum; a site-directed mutagenesis; antineoplastic effect of L-asparaginase; hTERT subunit of telomerase; telomerase.

MeSH terms

  • Amino Acid Sequence
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology*
  • Asparaginase / chemistry
  • Asparaginase / genetics
  • Asparaginase / metabolism
  • Asparaginase / pharmacology*
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Bacterial Proteins / pharmacology*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Escherichia coli / chemistry
  • Escherichia coli / enzymology
  • Escherichia coli / genetics
  • Gene Expression
  • HL-60 Cells
  • Humans
  • Jurkat Cells
  • Models, Molecular
  • Mutagenesis, Site-Directed
  • Pectobacterium carotovorum / chemistry
  • Pectobacterium carotovorum / enzymology
  • Pectobacterium carotovorum / genetics
  • Plasmids / chemistry
  • Plasmids / metabolism
  • Point Mutation*
  • Protein Structure, Secondary
  • Rhodospirillum rubrum / chemistry
  • Rhodospirillum rubrum / enzymology*
  • Rhodospirillum rubrum / genetics
  • Species Specificity
  • Structure-Activity Relationship
  • Telomerase / antagonists & inhibitors*
  • Telomerase / genetics
  • Telomerase / metabolism
  • Telomere / chemistry
  • Telomere / drug effects*
  • Wolinella / chemistry
  • Wolinella / enzymology
  • Wolinella / genetics

Substances

  • Antineoplastic Agents
  • Bacterial Proteins
  • TERT protein, human
  • Telomerase
  • Asparaginase