PfGBP: una proteína de unión al telómero de Plasmodium falciparum
PfGBP: A Plasmodium falciparum telomere binding protein
Palabras clave:
Telómero, proteínas de unión al telómero, telomerasa, hnRNPs, RRMs, extremo protuberante 3´, proteína recombinante, clonación (es)telomere, Telomere binding protein, telomerase, hnRPNs, RRMs, 3´overhang, recombinant protein, cloning. (en)
Descargas
Citas
Blackburn, E. Structure and function of telomeres. Nature. 1991. 350 (6319): 569-73.
Henderson, E.; Blackburn, E. An overhanging 3’ terminus is a conservated feature of telomeres. Mol. Cell. Biol. 1989. 9(1): 345-348.
De Lange, T. Shelterin: the protein complex that shapes and safeguards human telomeres. Genes. Dev. 2005. 19(18): 2100-2110.
Palm, W.; de Lange, T. How Shelterin Protects Mammalian Telomeres. Annu. Rev. Genet. 2008. 42: 301-334.
Levy, M.; Allsopp, R.; Futcher, A.; Greider, C.; Harley, C. Telomere end replication problem and cell aging. J. Mol. Biol. 1992. 225: 951-60.
Prescott, J.; Blackburn, E. Telomerase: Dr Jekyll or Mr Hyde? Curr. Opin. Gen. Develop. 1999. 9: 368-373.
Greider, C.; Blackburn, E. Identification of a specific telomere terminal transferase activity in Tetrahymena extracts. Cell. 1985. 43: 405-413.
Kim, N.; Piatyszek, M.; Prowse, K. Specific association on human telomerase activity with immortal cells and cancer. Science. 1994. 266: 2011-15.
Shampay, J.; Blackburn, E. Generation of telomere-length heterogeneity in Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. USA. 1988. 85: 534-8.
Bianchi, A.; Shore, D. How telomerase reaches its end: mechanism of telomerase regulation by the telomeric complex. Mol. Cell. 2008. 31: 153-65.
Birney, E.; Kumar, S.; Krainer, A. Analysis of the RNA-recognition motif RS and RGG domains: Conservation in metazoan pre-mRNA splicing factors. Nucleic. Acids. Res. 1993. 21: 5803–5816.
He, Y.; Smith, R. Nuclear functions of heterogeneous nuclear ribonucleoproteins A/B. Cell. Mol. Life. Sci. 2009. 66: 1239-56.
Fiset, S.; Chabot, B. hnRNP A1 may interact simultaneously with telomeric DNA and the human telomerase RNA in vitro. Nucleic. Acids. Res. 2001. 29: 2268-75.
Zhang, Q.; Manche, L.; Xu, R.; Krainer, A. hnRNP A1 associates with telomere ends and stimulates telomerase activity. RNA. 2006. 12: 1116–1128.
Moran-Jones, K.; Wayman, L.; Kennedy, D.; Reddel, R.; Snee, M.; Smith, R. hnRNP A2, a potential ssDNA/RNA molecular adapter at the telomere. Nucleic. Acids. Res. 2005. 19: 486-96.
Huang, P.; Hung, S.; Wang, T. Telomeric DNA-binding activities of heterogeneous nuclear ribonucleoprotein A3 in vitro and in vivo. Biochim. Biophys. Acta. 2010. 1803: 1164-74.
Chen, L.; Lingner, J. AUF1/HnRNP D RNA binding protein functions in telomere maintenance. J. Mol. Cell. 2012. 47: 1-2.
Enokizono, Y.; Konishi, Y.; Nagata, K.; Ouhashi, K.; Uesugi, S.; Ishikawa, F.; Katahira, M. Structure of hnRNP D complexed with single-stranded telomere DNA and unfolding of the quadruplex by heterogeneous nuclear ribonucleoprotein D. J. Biol. Chem. 2005. 280: 18862–18870.
Nagata, T.; Takada, Y.; Ono, A.; Nagata, K.; Konishi, Y.; Nukina, T.; Ono, M.; Matsugami, A.; Furukawa, A.; Fujimoto, N.; Fukuda, H.; Nakagama, H.; Katahira, M. Elucidation of the mode of interaction in the UP1–telomerase RNA–telomeric DNA ternary complex which serves to recruit telomerase to telomeric DNA and to enhance the telomerase activity. Nucleic. Acids. Res. 2008. 36: 6816–6824.
Wang, F.; Tang, M.; Zeng, Z.; Wu, R.; Xue, Y.; Hao, Y.; Pang, D.; Zhao, Y.; Tan, Z. Telomere- and telomerase-interacting protein that unfolds telomere G-quadruplex and promotes telomere extension in mammalian cells. Proc. Natl. Acad. Sci. USA. 2012. 109: 20413-8.
Wang, Q.; Liu, J.; Chen, Z.; Zheng, K.; Chen, C.; Hao, Y.; Tan Z. G-quadruplex formation at the 3′ end of telomere DNA inhibits its extension by telomerase, polymerase and unwinding by helicase. Nucleic. Acids. Res. 2011. 39: 6229–6237.
Ford, L.; Suh, J.; Wright, W.; Shay, J. Heterogeneous nuclear ribonucleoproteins C1 and C2 associate with the RNA component of human telomerase. Mol. Cell. Biol. 2000. 20: 9084–9091.
Ford, L.; Wright, W.; Shay, J. A model for heterogeneous nuclear ribonucleoproteins in telomere and telomerase regulation. Oncogene. 2002. 21: 580–583.
Petracek, M.; Konkel, L.; Kable, M.; Berman J. A Chlamydomonas protein that binds single-stranded G-strand telomere DNA. EMBO. J. 1994. 13: 3648-58.
Johnston, S.; Lew, J.; Berman, J. Gbp1p, a protein with RNA recognition motifs, binds single-stranded telomeric DNA and changes its binding specificity upon dimerization. Mol. Cell. Biol. 1999. 19: 923–33.
Konkel, L.; Enomoto, S.; Chamberlai, E.; McCune-Zierath, P.; Iyadura, S.; Berman J. A class of single-stranded telomeric DNA binding proteins required for Rap1p localization in yeast nuclei. Proc. Natl. Acad. Sci. USA. 1995. 92: 5558–5562.
Lee-Soety, J.; Jones, J.; MacGibeny, M.; Remaly, E.; Daniels, L.; Ito, A.; Jean, J.; Radecki, H.; Spencer, S. Yeast hnRNP-related proteins contribute to the maintenance of telomeres. Biochem. Biophys. Res. Commun. 2012. 426: 12-7.
Liu, C.; Wang, L.; Lancto, C.; Abrahamsen, M. Characterization of a Cryptosporidium parvum protein that binds single-stranded G-strand telomeric DNA. Mol. Biochem. Parasitol. 2009. 165: 132-41.
Janse, C.; van der Klooster, P.; van der Kaay, H.; van der Ploeg, M.; Overdulve, J. Mitomycin-C is an unreliable inhibitor for study of DNA synthesis in Plasmodium. Mol Biochem. Parasitol. 1986. 21: 33-6.
Aldous, W.; Martin, R.; and Kyle, D. Stage specific detection and inhibition studies of Plasmodium falciparum telomerase. Mol. Biochem. Parasitol. 1998. 95: 281-285.
Bottius, E.; Bakhsis, N.; and Sherf, A. Plasmodium falciparum telomerase: de novo telomere addition to telomeric and nontelomeric sequences and role in chromosome healing. Mol. Cell. Biol. 1998. 18: 919-925.
Raj, D.; Das, B.; Dash, A.; Supakar, P.Identification of telomerase activity in gametocytes of Plasmodium falciparum. Biochem. Biophys. Res. Commun. 2003. 309: 685-8.
Tamura, K.; Stecher, G.; Peterson, D.; Filipski, A.; and Kumar, S. MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0. Mol. Biol. Evolution. 2013. 30: 2725-2729.
Bradford, M. A rapid and sensitive method for quantitation of micrograms quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 1976. 72: 248-54.
Fayer, R.; Xiao, L. Cryptosporidium and cryptosporidiosis. 2a Edición. Boca Raton, FL: CRC Press, Inc. pp 11-20. 2007.
Zhao, N.; Gong, P.; Li, Z.; Cheng, B.; Li, J.; Yang, Z.; Li, H.; Yang, J.; Zhang, G.; Zhang, X. Identification of a telomeric DNA-binding protein in Eimeria tenella. Biochem. Biophys. Res. Commun. 2014. 451: 599-602.
Hirata, Y.; Suzuki, C.; Sakai, S. Characterization and gene cloning of telomere-binding protein from tobacco BY-2 cells. Plant. Physiol. Biochem. 2004. 42: 7–14.
Lee, Y.; Kim, W. Tobacco GTBP1, a Homolog of Human Heterogeneous Nuclear Ribonucleoprotein, Protects Telomeres from Aberrant Homologous Recombination. Plant. Cell. 2010. 22: 2781–2795.
Lee, Y.; Kim, W. Telomerase-dependent 3' G-strand overhang maintenance facilitates GTBP1-mediated telomere protection from misplaced homologous recombination. Plant. Cell. 2013. 25: 1329-42.
Licencia
Los autores/as conservarán sus derechos de autor y garantizarán a la revista el derecho de primera publicación de su obra, el cuál estará simultáneamente sujeto a la Licencia de reconocimiento de Creative Commons (CC. Atribución 4.0) que permite a terceros compartir la obra siempre que se indique su autor y su primera publicación en esta revista.
Los autores/as podrán adoptar otros acuerdos de licencia no exclusiva de distribución de la versión de la obra publicada (p. ej.: depositarla en un archivo telemático institucional o publicarla en un volumen monográfico) siempre que se indique la publicación inicial en esta revista.
Se permite y recomienda a los autores/as difundir su obra a través de Internet (p. ej.: en archivos telemáticos institucionales o en su página web) antes y durante el proceso de envío, lo cual puede producir intercambios interesantes y aumentar las citas de la obra publicada. (Véase El efecto del acceso abierto).
