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Remarkably, >30% of the differentially expressed genes exhibited a male or female expression bias.
Our finding that 31% of the expressed genes (>6700 transcripts) had a male or female expression bias (confirmed by permutation analysis) lends support for the role of the sex chromosomes in global gene regulation.
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In willows, inconstant males suggest that the supression of female expression in a male genotype is labile, depending on environmental conditions (Mosseler and Zsuffa, 1989).
In the studied S. subfragilis, genetic, epigenetic and cytoplasmic changes in the factor supressing female expression in males may be responsible for the occurance of hermaphrodites.
In "only F and H years", for example, "biased to F years" means that number of years when female expression was observed are more than that when hermaphroditic expression was observed.
In hermaphrodites, for example, sub-category "only F and M years" means that there are both years when female expression was observed and years when male expression was observed.
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The X-chromosome of T. castaneum is known to be enriched for female expression-biased genes [ 17].
Fig. S11 Male-female expression distances in faster aging and slower aging females.
In contrast, X. vesparum genes mapping to Tribolium chromosome 4 show significantly lower male/female expression ratios, using both the adult and larvae female sample (fig. 3).
In both lineages, the rate of protein evolution correlated positively with the male/female expression ratio.
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