Cell cycle-dependent expression of γ-tubulin in the amicronuclear ciliate Tetrahymena pyriformis

被引:8
|
作者
Joachimiak, Ewa
Pucciarelli, Sandra
Barchetta, Sabrina
Ballarini, Patrizia
Kaczanowska, Janina
Miceli, Cristina
机构
[1] Univ Camerino, Dept Mol Cellular & Anim Biol, I-62032 Camerino, Italy
[2] Warsaw Univ, Dept Cytophysiol, PL-02096 Warsaw, Poland
[3] Warsaw Univ, Dept Anim Physiol, PL-02096 Warsaw, Poland
关键词
cell cycle; cytoskeleton; gene expression regulation; tubulin; microtubules;
D O I
10.1016/j.protis.2006.08.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In ciliates, different microtubular structures are nucleated from diverse Microtubule Organizing Centers (MTOCs). gamma-Tubulin is a tubulin superfamily member that plays an essential role in microtubule nucleation at the MTOCs. However, little is known about mechanisms regulating the activity of gamma-tubulin on different MTOCs and during the cell cycle. In Tetrahymena thermophila, the alpha- and beta-tubulin expression is regulated mainly at the transcriptional level, and changes in the ratio of polymerized/unpolymerized tubulin dimers lead to an increase or decrease of alpha- and beta-tubulin transcription. This study deals with the characterization of gamma-tubulin in the amicronuclear ciliate Tetrahymena pyriformis. Sequence analysis revealed some specific substitutions in nucleotidebinding loops characteristic of the Tetrahymena genus and putative conserved phosphorylation sites located on the external surface of the gamma-tubulin molecule. gamma-Tubulin expression during the cell cycle, in the presence of microtubular poisons and after deciliation, was also characterized. We found that gamma-tubulin mRNA levels are correlated with basal body proliferation and gamma-tubulin nuclear localization. We also found that gamma-tubulin expression changes during anti-microtubular drugs treatment, but does not changes during reciliation. These findings suggest a relationship between the level of unpolymerized tubulin dimers and gamma-tubulin transcription. (c) 2006 Elsevier GmbH. All rights reserved.
引用
收藏
页码:39 / 50
页数:12
相关论文
共 50 条
  • [1] Cell cycle-dependent modulations of fenestrin expression in Tetrahymena pyriformis
    Joachimiak, Ewa
    Kiersnowska, Mauryla
    Jedynak, Katarzyna
    Majewska, Magdalena
    Fabczak, Hanna
    Fabczak, Stanislaw
    EUROPEAN JOURNAL OF PROTISTOLOGY, 2013, 49 (04) : 564 - 574
  • [2] ON CYCLE OF WATER EXPULSION VESICLE IN CILIATE TETRAHYMENA PYRIFORMIS
    CAMERON, IL
    BURTON, AL
    TRANSACTIONS OF THE AMERICAN MICROSCOPICAL SOCIETY, 1969, 88 (03): : 386 - &
  • [3] CONTROL OF TUBULIN AND ACTIN GENE-EXPRESSION IN TETRAHYMENA-PYRIFORMIS DURING THE CELL-CYCLE
    ZIMMERMAN, AM
    ZIMMERMAN, S
    THOMAS, J
    GINZBURG, I
    FEBS LETTERS, 1983, 164 (02) : 318 - 322
  • [4] TUBULIN GENES AND THEIR EXPRESSION IN THE PROTOZOA TETRAHYMENA-PYRIFORMIS
    RODRIGUESPOUSADA, C
    BARAHONA, I
    SOARES, H
    CYRNE, L
    PENQUE, D
    JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 1988, 9 (01) : 98 - 98
  • [5] CELL CYCLE-DEPENDENT EXPRESSION OF THE RETINOBLASTOMA GENE
    HASHIMOTO, T
    TAKAHASHI, R
    SHINDOH, H
    TANI, H
    NAKABAYASHI, H
    TAMAOKI, T
    FURUYAMA, J
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 454 - 454
  • [6] THERMORESISTANCE OF TETRAHYMENA PYRIFORMIS THROUGHOUT CELL CYCLE
    IRLINA, IS
    TSITOLOGIYA, 1972, 14 (01): : 69 - &
  • [7] Cell cycle-dependent expression and localization of human separase
    Chestukhin, A
    Litovchick, L
    DeCaprio, J
    FASEB JOURNAL, 2004, 18 (08): : C124 - C124
  • [8] EFFECT OF HIGH PRESSURE ON CELL CYCLE OF TETRAHYMENA PYRIFORMIS
    MACDONALD, AG
    JOURNAL OF PROTOZOOLOGY, 1967, S 14 : 42 - +
  • [9] LIPIDS OF MEMBRANEOUS CELL ORGANELLES ISOLATED FROM CILIATE, TETRAHYMENA-PYRIFORMIS
    JONAH, M
    ERWIN, JA
    BIOCHIMICA ET BIOPHYSICA ACTA, 1971, 231 (01) : 80 - &
  • [10] γ-Tubulin in Leishmania:: cell cycle-dependent changes in subcellular localization and heterogeneity of its isoforms
    Libusová, L
    Sulimenko, T
    Sulimenko, V
    Hozák, P
    Dráber, P
    EXPERIMENTAL CELL RESEARCH, 2004, 295 (02) : 375 - 386