Mol Cell Biol. 1994 September; 14(9): 5939-5949
A small family of elements with long inverted repeats is located near sites of developmentally regulated DNA rearrangement in Tetrahymena thermophila.
J M Wells,
J L Ellingson,
D M Catt,
P J Berger and
K M Karrer
Department of Biology, Brandeis University, Waltham, Massachusetts 02154.
ABSTRACT
Extensive DNA rearrangement occurs during the development of the somatic macronucleus from the germ line micronucleus in ciliated protozoans. The micronuclear junctions and the macronuclear product of a developmentally regulated DNA rearrangement in Tetrahymena thermophila, Tlr1, have been cloned. The intrachromosomal rearrangement joins sequences that are separated by more than 13 kb in the micronucleus with the elimination of moderately repeated micronucleus-specific DNA sequences. There is a long, 825-bp, inverted repeat near the micronuclear junctions. The inverted repeat contains two different 19-bp tandem repeats. The 19-bp repeats are associated with each other and with DNA rearrangements at seven locations in the micronuclear genome. Southern blot analysis is consistent with the occurrence of the 19-bp repeats within pairs of larger repeated sequences. Another family member was isolated. The 19-mers in that clone are also in close proximity to a rearrangement junction. We propose that the 19-mers define a small family of developmentally regulated DNA rearrangements having elements with long inverted repeats near the junction sites. We discuss the possibility that transposable elements evolve by capture of molecular machinery required for essential cellular functions.
Mol Cell Biol. 1994 September; 14(9): 5939-5949
This article has been cited by other articles:
-
Fillingham, J. S., Thing, T. A., Vythilingum, N., Keuroghlian, A., Bruno, D., Golding, G. B., Pearlman, R. E.
(2004). A Non-Long Terminal Repeat Retrotransposon Family Is Restricted to the Germ Line Micronucleus of the Ciliated Protozoan Tetrahymena thermophila. Eukaryot Cell
3: 157-169
[Abstract]
[Full Text]
-
Wuitschick, J. D., Karrer, K. M.
(2003). Diverse Sequences within Tlr Elements Target Programmed DNA Elimination in Tetrahymena thermophila. Eukaryot Cell
2: 678-689
[Abstract]
[Full Text]
-
Wuitschick, J. D., Gershan, J. A., Lochowicz, A. J., Li, S., Karrer, K. M.
(2002). A novel family of mobile genetic elements is limited to the germline genome in Tetrahymena thermophila. Nucleic Acids Res
30: 2524-2537
[Abstract]
[Full Text]
-
Karrer, K. M., VanNuland, T. A.
(2002). Methylation of adenine in the nuclear DNA of Tetrahymena is internucleosomal and independent of histone H1. Nucleic Acids Res
30: 1364-1370
[Abstract]
[Full Text]
-
Fillingham, J. S., Bruno, D., Pearlman, R. E.
(2001). Cis-acting requirements in flanking DNA for the programmed elimination of mse2.9: a common mechanism for deletion of internal eliminated sequences from the developing macronucleus of Tetrahymena thermophila. Nucleic Acids Res
29: 488-498
[Abstract]
[Full Text]
-
Gershan, J. A., Karrer, K. M.
(2000). A family of developmentally excised DNA elements in Tetrahymena is under selective pressure to maintain an open reading frame encoding an integrase-like protein. Nucleic Acids Res
28: 4105-4112
[Abstract]
[Full Text]
-
Patil, N. S., Karrer, K. M.
(2000). A developmentally regulated deletion element with long terminal repeats has cis-acting sequences in the flanking DNA. Nucleic Acids Res
28: 1465-1472
[Abstract]
[Full Text]
-
Karrer, K. M., VanNuland, T. A.
(1999). Nucleosome Positioning Is Independent of Histone H1 in Vivo. J. Biol. Chem.
274: 33020-33024
[Abstract]
[Full Text]
-
Chalker, D. L., La Terza, A., Wilson, A., Kroenke, C. D., Yao, M.-C.
(1999). Flanking Regulatory Sequences of the Tetrahymena R Deletion Element Determine the Boundaries of DNA Rearrangement. Mol. Cell. Biol.
19: 5631-5641
[Abstract]
[Full Text]
-
Saveliev, S V, Cox, M M
(1995). Transient DNA breaks associated with programmed genomic deletion events in conjugating cells of Tetrahymena thermophila.. Genes Dev.
9: 248-255
[Abstract]
Copyright © 1994 by the American Society for Microbiology. All rights reserved.