Sequence Finishing and Mapping of Drosophila melanogaster Heterochromatin

Author:

Hoskins Roger A.1234,Carlson Joseph W.1234,Kennedy Cameron1234,Acevedo David1234,Evans-Holm Martha1234,Frise Erwin1234,Wan Kenneth H.1234,Park Soo1234,Mendez-Lago Maria1234,Rossi Fabrizio1234,Villasante Alfredo1234,Dimitri Patrizio1234,Karpen Gary H.1234,Celniker Susan E.1234

Affiliation:

1. Department of Genome and Computational Biology, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

2. Centro de Biologia Molecular Severo Ochoa, CSIC-UAM, Cantoblanco 28049, Madrid, Spain.

3. Dipartimento di Genetica e Biologia Molecolare “Charles Darwin,” Universita “La Sapienza,” 00185 Roma, Italy.

4. Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.

Abstract

Genome sequences for most metazoans and plants are incomplete because of the presence of repeated DNA in the heterochromatin. The heterochromatic regions of Drosophila melanogaster contain 20 million bases (Mb) of sequence amenable to mapping, sequence assembly, and finishing. We describe the generation of 15 Mb of finished or improved heterochromatic sequence with the use of available clone resources and assembly methods. We also constructed a bacterial artificial chromosome–based physical map that spans 13 Mb of the pericentromeric heterochromatin and a cytogenetic map that positions 11 Mb in specific chromosomal locations. We have approached a complete assembly and mapping of the nonsatellite component of Drosophila heterochromatin. The strategy we describe is also applicable to generating substantially more information about heterochromatin in other species, including humans.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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