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Morgante, F.

Publications and source records attributed to Morgante, F..

2 recordsLinked to original sources

Leveraging multiple layers of data to predict Drosophila complex traits

An important challenge in genetics is to be able to predict complex traits accurately. Despite recent advances, prediction accuracy for most complex traits remains low. Here, we used the Drosophila Genetic Reference Panel (DGRP), a collection of 200 lines with whole-genome sequences and deep RNA sequencing data, to evaluate the usefulness of using high-quality gene expression levels compared to relying on genotypes for predicting three complex traits. We found that expression levels provided higher accuracy than genotypes for starvation resistance, similar accuracy for chill coma recovery, and lower accuracy for startle response. Models including both genotype and expressions levels did not outperform the best single component model. However, accuracy increased considerably for all the three traits when we included another layer of information, i.e., gene ontology (GO). We found that a limited number of GO terms, some of which had a clear biological interpretation, were strongly predictive of the traits. In summary, this study shows that integrating different sources of information can improve prediction accuracy, especially when large samples are not available.

genetics

Gene Expression Networks in the Drosophila Genetic Reference Panel

A major challenge in modern biology is to understand how naturally occurring variation in DNA sequences affects complex organismal traits through networks of intermediate molecular phenotypes. Here, we performed deep RNA sequencing of 200 Drosophila Genetic Reference Panel inbred lines with complete genome sequences, and mapped expression quantitative trait loci for annotated genes, novel transcribed regions (most of which are long noncoding RNAs), transposable elements and microbial species. We identified host variants that affect expression of transposable elements, independent of their copy number, as well as microbiome composition. We constructed sex-specific expression quantitative trait locus regulatory networks. These networks are enriched for novel transcribed regions and target genes in heterochromatin and euchromatic regions of reduced recombination, and genes regulating transposable element expression. This study provides new insights regarding the role of natural genetic variation in regulating gene expression and generates testable hypotheses for future functional analyses.

genomics