Development and analysis of a germline BAC resource for the sea lamprey, a vertebrate that undergoes substantial chromatin diminution

Jeramiah J. Smith, Andrew B. Stuart, Tatjana Sauka-Spengler, Sandra W. Clifton, Chris T. Amemiya

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

Over the last several years, the sea lamprey (Petromyzon marinus) has grown substantially as a model for understanding the evolutionary fundaments and capacity of vertebrate developmental and genome biology. Recent work on the lamprey genome has resulted in a preliminary assembly of the lamprey genome and led to the realization that nearly all somatic cell lineages undergo extensive programmed rearrangements. Here we describe the development of a bacterial artificial chromosome (BAC) resource for lamprey germline DNA and use sequence information from this resource to probe the subchromosomal structure of the lamprey genome. The arrayed germline BAC library represents ∼10× coverage of the lamprey genome. Analyses of BAC-end sequences reveal that the lamprey genome possesses a high content of repetitive sequences (relative to human), which show strong clustering at the subchromosomal level. This pattern is not unexpected given that the sea lamprey genome is dispersed across a large number of chromosomes (n∼99) and suggests a low-copy DNA targeting strategy for efficiently generating informative paired-BAC-end linkages from highly repetitive genomes. This library therefore represents a new and biologically informed resource for understanding the structure of the lamprey genome and the biology of programmed genome rearrangement.

Original languageEnglish
Pages (from-to)381-389
Number of pages9
JournalChromosoma
Volume119
Issue number4
DOIs
StatePublished - Aug 2010

Bibliographical note

Funding Information:
Acknowledgments This work was supported by the National Institutes of Health [grant number GM079492] and the National Science Foundation [grant number MCB-0719558] to CTA. This work was supported by the National Institutes of Health [grant number T32-HG00035, F32-GM087919] to JJS. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of NIH.

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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