Evidence map›Paper›PMID 12582127›Full record

ArticleEukaryotic cell2003

Tec3, a new developmentally eliminated DNA element in Euplotes crassus.

Mary Ellen Jacobs, Adolfo Sánchez-Blanco, Laura A Katz, Lawrence A Klobutcher

Abstract read
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Article in Eukaryotic cell, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Mary Ellen JacobsDepartment of Biochemistry, University of Connecticut Health Center, Farmington, Connecticut 06030, USA. jacobs@neuron.uchc.edu
Adolfo Sánchez-Blanco
Laura A Katz
Lawrence A Klobutcher

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More than 100,000 interstitial segments of DNA (internal eliminated sequences [IESs]) are excised from the genome during the formation of a new macronucleus in Euplotes crassus. IESs include unique sequence DNA as well as two related families of transposable elements, Tec1 and Tec2. Here we describe a new class of E. crassus transposons, Tec3, which is present in 20 to 30 copies in the micronuclear genome. Tec3 elements have long inverted terminal repeats and contain a degenerate open reading frame encoding a tyrosine-type recombinase. One characterized copy of Tec3 (Tec3-1) is 4.48 kbp long, has 1.23-kbp inverted terminal repeats, and resides within the micronuclear copy of the ribosomal protein L29 gene (RPL29). The 23 bp at the extreme ends of this element are very similar to those in other E. crassus IESs and, like these other IESs, Tec3-1 is excised during the polytene chromosome stage of macronuclear development to generate a free circular form with an unusual junction structure. In contrast, a second cloned element, Tec3-2, is quite similar to Tec3-1 but lacks the terminal 258 bp of the inverted repeats, so that its ends do not resemble the other E. crassus IES termini. The Tec3-2 element appears to reside in a large segment of the micronuclear genome that is subject to developmental elimination. Models for the origins of these two types of Tec3 elements are presented, along with a discussion of how some members of this new transposon family may have come to be excised by the same machinery that removes other E. crassus IESs.

Indexed as

AnimalsBase SequenceDNADNA NucleotidyltransferasesDNA Transposable ElementsEuplotesEvolution, MolecularGenomeMolecular Sequence DataMolecular StructurePhylogenyProtozoan ProteinsRecombinasesRecombination, GeneticRibosomal ProteinsSequence Homology, Nucleic AcidDNADNA NucleotidyltransferasesDNA Transposable ElementsL29 protein, Giardia lambliaProtozoan ProteinsRecombinasesRibosomal Proteins

Identifiers

PMID12582127
PMCPMC141165

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.