Abstract

The Muller F element (4.2 Mb, ~80 protein-coding genes) is an unusual autosome of Drosophila melanogaster; it is mostly heterochromatic with a low recombination rate. To investigate how these properties impact the evolution of repeats and genes, we manually improved the sequence and annotated the genes on the D. erecta, D. mojavensis, and D. grimshawi F elements and euchromatic domains from the Muller D element. We find that F elements have greater transposon density (25–50%) than euchromatic reference regions (3–11%). Among the F elements, D. grimshawi has the lowest transposon density (particularly DINE-1: 2% vs. 11–27%). F element genes have larger coding spans, more coding exons, larger introns, and lower codon bias. Comparison of the Effective Number of Codons with the Codon Adaptation Index shows that, in contrast to the other species, codon bias in D. grimshawi F element genes can be attributed primarily to selection instead of mutational biases, suggesting that density and types of transposons affect the degree of local heterochromatin formation. F element genes have lower estimated DNA melting temperatures than D element genes, potentially facilitating transcription through heterochromatin. Most F element genes (~90%) have remained on that element, but the F element has smaller syntenic blocks than genome averages (3.4–3.6 vs. 8.4–8.8 genes per block), indicating greater rates of inversion despite lower rates of recombination. Overall, the F element has maintained characteristics that are distinct from other autosomes in the Drosophila lineage, illuminating the constraints imposed by a heterochromatic milieu.

Highlights

  • The Muller F element (4.2 Mb, ~80 protein-coding genes) is an unusual autosome of Drosophila melanogaster; it is mostly heterochromatic with a low recombination rate

  • Quality assessments of the Comparative Analysis Freeze 1 (CAF1) assemblies (Drosophila 12 Genomes Consortium et al 2007) led us to improve the D. mojavensis F element, the D. grimshawi F element, and the D. mojavensis euchromatic reference region from the D element to a quality standard that is similar to those used for the mouse genome project

  • Detailed alignments between the CAF1 and the improved regions are available through the “D. mojavensis CAF1 Difference” and “D. grimshawi CAF1 Difference” tracks on the Genomics Education Partnership (GEP) UCSC Genome Browser

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Summary

Introduction

The Muller F element (4.2 Mb, ~80 protein-coding genes) is an unusual autosome of Drosophila melanogaster; it is mostly heterochromatic with a low recombination rate To investigate how these properties impact the evolution of repeats and genes, we manually improved the sequence and annotated the genes on the D. erecta, D. mojavensis, and D. grimshawi F elements and euchromatic domains from the Muller D element. With an estimated size of 4.2 Mb overall, the Drosophila melanogaster Muller F element, ( known as the dot chromosome, or the fourth chromosome in that species) is unusual in that it appears entirely heterochromatic by most criteria, but the distal 1.3 Mb has a gene density and fraction of active genes (~50% in S2 cells) that are similar to the euchromatic regions of the D. melanogaster genome (Riddle et al 2009, 2012). Most of these analyses only focused on the Muller elements A–E and the properties of the F element generally have not been examined carefully

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