Across species, animals have diverse sex determination pathways, each consisting of a hierarchical cascade of genes and its associated regulatory mechanism. Houseflies have a distinctive polymorphic sex determination system in which a dominant male determiner, the M-factor, can reside on any of the chromosomes. We identified a gene, (), as the M-factor. originated from a duplication of the spliceosomal factor gene (). Targeted disruption results in complete sex reversal to fertile females because of a shift from male to female expression of the downstream genes and The presence of on different chromosomes indicates that translocated to different genomic sites. Thus, an instructive signal in sex determination can arise by duplication and neofunctionalization of an essential splicing regulator.
A gene function prediction method suitable for the design of targeted RNAi libraries is described and used to predict chromosome condensation genes. Systematic experimental validation of candidate genes in a focused RNAi screen by automated microscopy and quantitative image analysis reveals many new chromosome condensation factors.
Determining the network of physical protein associations is an important first step in developing mechanistic evidence for elucidating biological pathways. Despite rapid advances in the field of high throughput experiments to determine protein interactions, the majority of associations remain unknown. Here we describe computational methods for significantly expanding protein association networks. We describe methods for integrating multiple independent sources of evidence to obtain higher quality predictions and we compare the major publicly available resources available for experimentalists to use.
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