- THIS ARTICLE
- Full Text (PDF)
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via HighWire
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Medhora, M.
- Articles by Hartl, D. L.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Medhora, M.
- Articles by Hartl, D. L.
Genetics, Vol 128, 311-318, Copyright © 1991
INVESTIGATIONS |
Molecular and Functional Analysis of the mariner Mutator Element Mos1 in Drosophila
M. Medhora, K. Maruyama and D. L. Hartl
Department of Genetics, Washington University School of Medicine, St. Louis, Missouri 63110-1095
The white-peach allele in Drosophila results from insertion of the transposable element mariner. The particular copy that is inserted in white-peach is an inactive copy referred to as the peach element. The peach element is excised at a high rate in the presence of active copies of mariner located elsewhere in the genome, and the excision of peach in somatic cells is recognized phenotypically by the occurrence of eye-color mosaicism in white-peach flies. Active mariner elements identified by their ability to induce high levels of white-peach mosaicism are denoted Mos (Mosaic) factors. We have sequenced and functionally analyzed the factor Mos1 originally identified in Drosophila mauritiana. The Mos1 element is 1286 base pairs in length, the same length as the peach element. It differs from the peach element in 11 nucleotide positions distributed throughout its length, including four amino acid replacements in the long open reading frame. Analysis of chimeric constructs between Mos1 and peach implies that functionally important differences occur in both the 5' and 3' halves of Mos1. A mariner element identical in sequence to Mos1 yields lower levels of mosaicism in transformants, implying that adjacent flanking sequences have important effects on Mos1 activity. Another mariner element, designated Ma351, isolated from a nonmosaic strain of D. mauritiana, differs from Mos1 in just three nucleotide positions. When introduced into the germline, Ma351 yields various levels of white-peach mosaicism depending on insertion site. These results imply that the activity of mariner elements is determined jointly by their own nucleotide sequences, by the effects of adjacent flanking sequences, and by longer-range position effects.
This article has been cited by other articles:
![]() |
D. G. Moerman and R. J. Barstead Towards a mutation in every gene in Caenorhabditis elegans Brief Funct Genomic Proteomic, May 1, 2008; 7(3): 195 - 204. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. D. Tinsley Profile of Daniel L. Hartl PNAS, May 29, 2007; 104(22): 9111 - 9113. [Full Text] [PDF] |
||||
![]() |
J. C. Silva, F. Bastida, S. L. Bidwell, P. J. Johnson, and J. M. Carlton A Potentially Functional Mariner Transposable Element in the Protist Trichomonas vaginalis Mol. Biol. Evol., January 1, 2005; 22(1): 126 - 134. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Leal, A. Acosta-Serrano, J. Morris, and G. A. M. Cross Transposon Mutagenesis of Trypanosoma brucei Identifies Glycosylation Mutants Resistant to Concanavalin A J. Biol. Chem., July 9, 2004; 279(28): 28979 - 28988. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. G. Barry, D. J. Witherspoon, and D. J. Lampe A Bacterial Genetic Screen Identifies Functional Coding Sequences of the Insect mariner Transposable Element Famar1 Amplified From the Genome of the Earwig, Forficula auricularia Genetics, February 1, 2004; 166(2): 823 - 833. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Jasinskiene, C. J. Coates, A. Ashikyan, and A. A. James High efficiency, site-specific excision of a marker gene by the phage P1 cre-loxP system in the yellow fever mosquito, Aedes aegypti Nucleic Acids Res., November 15, 2003; 31(22): e147 - e147. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M. Carlson, A. J. Dupuy, S. Fritz, K. J. Roberg-Perez, C. F. Fletcher, and D. A. Largaespada Transposon Mutagenesis of the Mouse Germline Genetics, September 1, 2003; 165(1): 243 - 256. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. R. Lozovsky, D. Nurminsky, E. A. Wimmer, and D. L. Hartl Unexpected Stability of mariner Transgenes in Drosophila Genetics, February 1, 2002; 160(2): 527 - 535. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Zhang, A. Dawson, and D. J. Finnegan DNA-binding activity and subunit interaction of the mariner transposase Nucleic Acids Res., September 1, 2001; 29(17): 3566 - 3575. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. E. J. Fischer, E. Wienholds, and R. H. A. Plasterk Regulated transposition of a fish transposon in the mouse germ line PNAS, May 24, 2001; (2001) 121569298. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. L. Hartl Discovery of the Transposable Element Mariner Genetics, February 1, 2001; 157(2): 471 - 476. [Full Text] |
||||
![]() |
B. T. Beerntsen, A. A. James, and B. M. Christensen Genetics of Mosquito Vector Competence Microbiol. Mol. Biol. Rev., March 1, 2000; 64(1): 115 - 137. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. R. O. Tosi and S. M. Beverley cis and trans factors affecting Mos1 mariner evolution and transposition in vitro, and its potential for functional genomics Nucleic Acids Res., February 1, 2000; 28(3): 784 - 790. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Jarvik and K. G. Lark Characterization of Soymar1, a Mariner Element in Soybean Genetics, July 1, 1998; 149(3): 1569 - 1574. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. J. Coates, N. Jasinskiene, L. Miyashiro, and A. A. James Mariner transposition and transformation of the yellow fever mosquito, Aedes aegypti PNAS, March 31, 1998; 95(7): 3748 - 3751. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. J. Gueiros-Filho and S. M. Beverley Trans-kingdom Transposition of the Drosophila Element mariner Within the Protozoan Leishmania Science, June 13, 1997; 276(5319): 1716 - 1719. [Abstract] [Full Text] |
||||
![]() |
A. R. Lohe, D. De Aguiar, and D. L. Hartl Mutations in the mariner transposase: The D,D(35)E consensus sequence is nonfunctional PNAS, February 18, 1997; 94(4): 1293 - 1297. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. E. J. Fischer, E. Wienholds, and R. H. A. Plasterk Regulated transposition of a fish transposon in the mouse germ line PNAS, June 5, 2001; 98(12): 6759 - 6764. [Abstract] [Full Text] [PDF] |
||||







