Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (9)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Tu, Z.
Right arrow Articles by Orphanidis, S. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tu, Z.
Right arrow Articles by Orphanidis, S. P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Biology and Evolution 18:893-895 (2001)
© 2001 Society for Molecular Biology and Evolution


LETTER

Microuli, a Family of Miniature Subterminal Inverted-Repeat Transposable Elements (MSITEs): Transposition Without Terminal Inverted Repeats

Zhijian TuGo,* and Stephanos P. Orphanidis{dagger}

*Department of Biochemistry, Virginia Polytechnic Institute and State University; and
{dagger}Department of Biochemistry, University of Arizona

The first Microuli element, Microuli-Aa1, was discovered as a 209-bp insertion in the 5' long terminal repeat of a retrotransposon named Mosqcopia-Aa2 (unpublished data, GenBank AY009101) in the yellow fever mosquito, Aedes aegypti. As shown in figure 1A, the Microuli insertion resulted in a TTAA target duplication, indicating past mobility of the element. To further characterize this mobile element, we screened an A. aegypti genomic library, using a digoxigenin-labeled single-stranded DNA probe generated by asymmetric PCR using the entire Microuli-Aa1 as the template. The library construction, probe labeling, and library screening procedures were as previously described (Tu 2000Citation ). The final washing stringency was 0.5 x SSC with 0.1% SDS at 55°C, which allows approximately 15%–25% mismatch (Meinkoth and Wahl 1984Citation ). Because 462 positive plaques were identified among 64,000 total plaques screened, it was estimated using a previously described calculation method (Tu 2000Citation ) that there were . . . [Full Text of this Article]

Acknowledgements

Footnotes

literature cited


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J HeredHome page
E. W. Chambers, J. K. Meece, J. A. McGowan, D. D. Lovin, R. R. Hemme, D. D. Chadee, K. McAbee, S. E. Brown, D. L. Knudson, and D. W. Severson
Microsatellite Isolation and Linkage Group Identification in the Yellow Fever Mosquito Aedes aegypti
J. Hered., May 1, 2007; 98(3): 202 - 210.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
S. Berkner and G. Lipps
An Active Nonautonomous Mobile Element in Sulfolobus islandicus REN1H1
J. Bacteriol., March 1, 2007; 189(5): 2145 - 2149.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
G. Yang and T. C. Hall
MAK, a computational tool kit for automated MITE analysis
Nucleic Acids Res., July 1, 2003; 31(13): 3659 - 3665.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
S. Zhang and G. Magnusson
Cellular Mobile Genetic Elements in the Regulatory Region of the Pneumotropic Mouse Polyomavirus Genome: Structure and Function in Viral Gene Expression and DNA Replication
J. Virol., March 15, 2003; 77(6): 3477 - 3486.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
A. J. Holyoake and M. G. Kidwell
Vege and Mar: Two Novel hAT MITE Families from Drosophila willistoni
Mol. Biol. Evol., February 1, 2003; 20(2): 163 - 167.
[Abstract] [Full Text] [PDF]