Abstract
Telomere lengths and telomerase activity were studied during the development of a model dioecious plant, Melandrium album (syn Silene latifolia). Telomeric DNA consisted of Arabidopsis-type TTTAGGG tandem repeats. The terminal positions of these repeats were confirmed by both Bal31 exonuclease degradation and in situ hybridization. Analysis of terminal restriction fragments in different tissues and ontogenetic stages showed that telomere lengths are stabilized precisely and do not change during plant growth and development. Telomerase activity tested by using a semiquantitative telomerase repeat amplification protocol correlated with cell proliferation in the tissues analyzed. Highest activity was found in germinating seedlings and root tips, whereas we observed a 100-fold decrease in telomerase activity in leaves and no activity in quiescent seeds. Telomerase also was found in mature pollen grains. Telomerase activity in tissues containing dividing cells and telomere length stability during development suggest their precise control during plant ontogenesis; however, the telomere length regulation mechanism could be unbalanced during in vitro dedifferentiation.
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- Allsopp R. C., Chang E., Kashefi-Aazam M., Rogaev E. I., Piatyszek M. A., Shay J. W., Harley C. B. Telomere shortening is associated with cell division in vitro and in vivo. Exp Cell Res. 1995 Sep;220(1):194–200. doi: 10.1006/excr.1995.1306. [DOI] [PubMed] [Google Scholar]
- Allsopp R. C., Vaziri H., Patterson C., Goldstein S., Younglai E. V., Futcher A. B., Greider C. W., Harley C. B. Telomere length predicts replicative capacity of human fibroblasts. Proc Natl Acad Sci U S A. 1992 Nov 1;89(21):10114–10118. doi: 10.1073/pnas.89.21.10114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Autexier C., Greider C. W. Telomerase and cancer: revisiting the telomere hypothesis. Trends Biochem Sci. 1996 Oct;21(10):387–391. [PubMed] [Google Scholar]
- Blackburn E. H. Structure and function of telomeres. Nature. 1991 Apr 18;350(6319):569–573. doi: 10.1038/350569a0. [DOI] [PubMed] [Google Scholar]
- Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
- Broun P., Ganal M. W., Tanksley S. D. Telomeric arrays display high levels of heritable polymorphism among closely related plant varieties. Proc Natl Acad Sci U S A. 1992 Feb 15;89(4):1354–1357. doi: 10.1073/pnas.89.4.1354. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bryan T. M., Englezou A., Gupta J., Bacchetti S., Reddel R. R. Telomere elongation in immortal human cells without detectable telomerase activity. EMBO J. 1995 Sep 1;14(17):4240–4248. doi: 10.1002/j.1460-2075.1995.tb00098.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burr B., Burr F. A., Matz E. C., Romero-Severson J. Pinning down loose ends: mapping telomeres and factors affecting their length. Plant Cell. 1992 Aug;4(8):953–960. doi: 10.1105/tpc.4.8.953. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bůzek J., Koutníková H., Houben A., Ríha K., Janousek B., Siroký J., Grant S., Vyskot B. Isolation and characterization of X chromosome-derived DNA sequences from a dioecious plant Melandrium album. Chromosome Res. 1997 Feb;5(1):57–65. doi: 10.1023/a:1011693603279. [DOI] [PubMed] [Google Scholar]
- Counter C. M., Avilion A. A., LeFeuvre C. E., Stewart N. G., Greider C. W., Harley C. B., Bacchetti S. Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity. EMBO J. 1992 May;11(5):1921–1929. doi: 10.1002/j.1460-2075.1992.tb05245.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Donnison I. S., Siroky J., Vyskot B., Saedler H., Grant S. R. Isolation of Y chromosome-specific sequences from Silene latifolia and mapping of male sex-determining genes using representational difference analysis. Genetics. 1996 Dec;144(4):1893–1901. doi: 10.1093/genetics/144.4.1893. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fajkus J., Kovarík A., Královics R. Telomerase activity in plant cells. FEBS Lett. 1996 Aug 12;391(3):307–309. doi: 10.1016/0014-5793(96)00757-0. [DOI] [PubMed] [Google Scholar]
- Fitzgerald M. S., McKnight T. D., Shippen D. E. Characterization and developmental patterns of telomerase expression in plants. Proc Natl Acad Sci U S A. 1996 Dec 10;93(25):14422–14427. doi: 10.1073/pnas.93.25.14422. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harley C. B., Futcher A. B., Greider C. W. Telomeres shorten during ageing of human fibroblasts. Nature. 1990 May 31;345(6274):458–460. doi: 10.1038/345458a0. [DOI] [PubMed] [Google Scholar]
- Heller K., Kilian A., Piatyszek M. A., Kleinhofs A. Telomerase activity in plant extracts. Mol Gen Genet. 1996 Sep 13;252(3):342–345. doi: 10.1007/BF02173780. [DOI] [PubMed] [Google Scholar]
- Kilian A., Stiff C., Kleinhofs A. Barley telomeres shorten during differentiation but grow in callus culture. Proc Natl Acad Sci U S A. 1995 Oct 10;92(21):9555–9559. doi: 10.1073/pnas.92.21.9555. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kirk K. E., Harmon B. P., Reichardt I. K., Sedat J. W., Blackburn E. H. Block in anaphase chromosome separation caused by a telomerase template mutation. Science. 1997 Mar 7;275(5305):1478–1481. doi: 10.1126/science.275.5305.1478. [DOI] [PubMed] [Google Scholar]
- Mantell L. L., Greider C. W. Telomerase activity in germline and embryonic cells of Xenopus. EMBO J. 1994 Jul 1;13(13):3211–3217. doi: 10.1002/j.1460-2075.1994.tb06620.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marcand S., Gilson E., Shore D. A protein-counting mechanism for telomere length regulation in yeast. Science. 1997 Feb 14;275(5302):986–990. doi: 10.1126/science.275.5302.986. [DOI] [PubMed] [Google Scholar]
- Meyne J., Moyzis R. K. In situ hybridization using synthetic oligomers as probes for centromere and telomere repeats. Methods Mol Biol. 1994;33:63–74. doi: 10.1385/0-89603-280-9:63. [DOI] [PubMed] [Google Scholar]
- Regad F., Lebas M., Lescure B. Interstitial telomeric repeats within the Arabidopsis thaliana genome. J Mol Biol. 1994 Jun 3;239(2):163–169. doi: 10.1006/jmbi.1994.1360. [DOI] [PubMed] [Google Scholar]
- Richards E. J., Ausubel F. M. Isolation of a higher eukaryotic telomere from Arabidopsis thaliana. Cell. 1988 Apr 8;53(1):127–136. doi: 10.1016/0092-8674(88)90494-1. [DOI] [PubMed] [Google Scholar]
- Zakian V. A. Telomeres: beginning to understand the end. Science. 1995 Dec 8;270(5242):1601–1607. doi: 10.1126/science.270.5242.1601. [DOI] [PubMed] [Google Scholar]
- Zentgraf U. Telomere-binding proteins of Arabidopsis thaliana. Plant Mol Biol. 1995 Feb;27(3):467–475. doi: 10.1007/BF00019314. [DOI] [PubMed] [Google Scholar]
- van Steensel B., de Lange T. Control of telomere length by the human telomeric protein TRF1. Nature. 1997 Feb 20;385(6618):740–743. doi: 10.1038/385740a0. [DOI] [PubMed] [Google Scholar]