Literature DB >> 9154003

What restricts the activity of mariner-like transposable elements.

D L Hartl1, E R Lozovskaya, D I Nurminsky, A R Lohe.   

Abstract

A number of mechanisms have recently been described that might be important in restricting the level of activity of mariner-like transposable elements (MLEs) in natural populations. These mechanisms include overproduction inhibition, in which increasing the dose of transposase decreases net activity. Another mechanism is mediated by certain missense mutations, in which a mutant transposase protein impairs the activity of the wild-type transposase in heterozygous mutant/nonmutant genotypes. A further mechanism is the potential for transposase titration by defective elements that retain transposase binding activity. The issue of regulation is not only of theoretical importance in understanding the molecular and evolutionary genetics of MLEs, but also of practical significance in learning how best to use MLEs in the germline transformation of insect pests and disease vectors.

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Year:  1997        PMID: 9154003     DOI: 10.1016/s0168-9525(97)01087-1

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  44 in total

1.  Discovery of the transposable element mariner.

Authors:  D Hartl
Journal:  Genetics       Date:  2001-02       Impact factor: 4.562

2.  Expression and post-transcriptional regulation of maize transposable element MuDR and its derivatives.

Authors:  G N Rudenko; V Walbot
Journal:  Plant Cell       Date:  2001-03       Impact factor: 11.277

3.  cis and trans factors affecting Mos1 mariner evolution and transposition in vitro, and its potential for functional genomics.

Authors:  L R Tosi; S M Beverley
Journal:  Nucleic Acids Res       Date:  2000-02-01       Impact factor: 16.971

4.  Early intermediates of mariner transposition: catalysis without synapsis of the transposon ends suggests a novel architecture of the synaptic complex.

Authors:  Karen Lipkow; Nicolas Buisine; David J Lampe; Ronald Chalmers
Journal:  Mol Cell Biol       Date:  2004-09       Impact factor: 4.272

5.  Mutational analysis of the N-terminal DNA-binding domain of sleeping beauty transposase: critical residues for DNA binding and hyperactivity in mammalian cells.

Authors:  Stephen R Yant; Julie Park; Yong Huang; Jacob Giehm Mikkelsen; Mark A Kay
Journal:  Mol Cell Biol       Date:  2004-10       Impact factor: 4.272

6.  Endogenous transposases affect differently Sleeping Beauty and Frog Prince transposons in fish cells.

Authors:  Jose Braulio Gallardo-Gálvez; Teresa Méndez; Julia Béjar; M Carmen Alvarez
Journal:  Mar Biotechnol (NY)       Date:  2010-12-01       Impact factor: 3.619

7.  Isolation and characterization of seventy-nine full-length mariner-like transposase genes in the Bambusoideae subfamily.

Authors:  Ming-Bing Zhou; Hao Zhong; Ding-Qin Tang
Journal:  J Plant Res       Date:  2010-12-17       Impact factor: 2.629

8.  Herpes simplex virus/Sleeping Beauty vector-based embryonic gene transfer using the HSB5 mutant: loss of apparent transposition hyperactivity in vivo.

Authors:  Suresh de Silva; Michael A Mastrangelo; Louis T Lotta; Clark A Burris; Zsuzsanna Izsvák; Zoltán Ivics; William J Bowers
Journal:  Hum Gene Ther       Date:  2010-10-22       Impact factor: 5.695

9.  A resurrected mammalian hAT transposable element and a closely related insect element are highly active in human cell culture.

Authors:  Xianghong Li; Hosam Ewis; Robert H Hice; Nirav Malani; Nicole Parker; Liqin Zhou; Cédric Feschotte; Frederic D Bushman; Peter W Atkinson; Nancy L Craig
Journal:  Proc Natl Acad Sci U S A       Date:  2012-10-22       Impact factor: 11.205

10.  Intra- and interspecies variation among Bari-1 elements of the melanogaster species group.

Authors:  R Moschetti; C Caggese; P Barsanti; R Caizzi
Journal:  Genetics       Date:  1998-09       Impact factor: 4.562

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