Abstract

BackgroundGerm cells in animals are highly specialized to preserve the genome. A distinct set of chromatin structures must be properly established in germ cells to maintain cell fate and genome integrity. We describe DNA-surface interactions in activated Caenorhabditis elegans oocytes that are revealed through the activity of an endogenous nuclease ('endocleavage’).ResultsOur analysis began with an unexpected observation that a majority (>50%) of DNA from ovulated but unfertilized C. elegans oocytes can be recovered in fragments of approximately 500 base pairs or shorter, cleaved at regular intervals (10 to 11 nt) along the DNA helix. In some areas of the genome, DNA cleavage patterns in these endoreduplicated oocytes appear consistent from cell-to-cell, indicating coherent rotational positioning of the DNA in chromatin. Particularly striking in this analysis are arrays of sensitive sites with a periodicity of approximately 10 bp that persist for several hundred base pairs of genomic DNA, longer than a single nucleosome core. Genomic regions with a strong bias toward a 10-nt periodic occurrence of A(n)/T(n) (so-called PATC regions) appear to exhibit a high degree of rotational constraint in endocleavage phasing, with a strong tendency for the periodic A(n)/T(n) sites to remain on the face of the helix protected from nuclease digestion.ConclusionThe present analysis provides evidence for an unusual structure in C. elegans oocytes in which genomic DNA and associated protein structures are coherently linked.

Highlights

  • Germ cells in animals are highly specialized to preserve the genome

  • A distinct set of chromatin structures must be properly established in germ cells to maintain cell fate and genome integrity [1,2]

  • Fragmented chromatin in activated fer-1(b232) C. elegans oocytes Ovulated but unfertilized oocytes have been a standard starting material for a variety of genomic and proteomic studies of C. elegans germline development [7,8,9]. These cells are a readily available germline tissue source from C. elegans, retaining transcriptional and proteomic characteristics of the oocyte lineage [8,9], certain features distinguish them from oocytes progressing to embryogenesis in the presence of fertilizing sperm

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Summary

Introduction

Germ cells in animals are highly specialized to preserve the genome. A distinct set of chromatin structures must be properly established in germ cells to maintain cell fate and genome integrity. We describe DNA-surface interactions in activated Caenorhabditis elegans oocytes that are revealed through the activity of an endogenous nuclease (‘endocleavage’). Germ cells in animals are highly specialized to preserve the genome. A distinct set of chromatin structures must be properly established in germ cells to maintain cell fate and genome integrity [1,2]. With the goal of understanding such structures in Caenorhabditis elegans, a number of groups have been applying combinations of genomics, biochemistry, and genetics (reviewed in [1]). C. elegans oocytes arrest at the diakinesis stage of meiotic prophase I. Oocyte chromosomes at this stage are highly condensed, giving rise to the characteristic

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