Volume 24, Issue 1 pp. 9-13
Rapid Communication
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Characterization of a mutagenic B1 retrotransposon insertion in the jittery mouse

Nicolas Gilbert

Corresponding Author

Nicolas Gilbert

Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan

Institut de Génétique Humaine, CNRS, UPR 1142, 141 rue de la Cardonille, 34396 Montpellier cedex 5, FranceSearch for more papers by this author
Jamee M. Bomar

Jamee M. Bomar

Mental Health Research Institute, University of Michigan Medical School, Ann Arbor, Michigan

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Margit Burmeister

Margit Burmeister

Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan

Mental Health Research Institute, University of Michigan Medical School, Ann Arbor, Michigan

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John V. Moran

John V. Moran

Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan

Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan

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First published: 27 May 2004
Citations: 20

Communicated by Haig H. Kazazian

Abstract

B1 elements are an abundant class of short interspersed elements (SINEs) in the mouse genome and mobilize by a process known as retrotransposition. Here, we report the characterization of a mutagenic B1 insertion into exon 4 of the Atcay gene, which was previously shown to be responsible for the jittery mouse. Mutations in the human ortholog of this gene, ATCAY, are responsible for Cayman ataxia. The B1 insertion is ∼150-bp long, ends in a 45–50-bp polyadenylic acid (poly A) tail, is flanked by a perfect 13-bp target-site duplication, and is inserted into a sequence that resembles a LINE-1 endonuclease consensus cleavage site. Computational analysis indicates that the mutagenic insertion is most closely related to elements of the B1-C subfamily, and we have identified two possible progenitor B1 sequences on mouse chromosome 19. Together, these data demonstrate that B1 retrotransposition is ongoing in the mouse genome and is consistent with the hypothesis that the reverse transcriptase and endonuclease encoded by LINE-1 elements mediate B1 mobility. Hum Mutat 24:9–13, 2004. © 2004 Wiley-Liss, Inc.

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