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Sex-contingent face after-effects suggest distinct neural populations code male and female faces.

ABSTRACT: Exposure to faces biases perceptions of subsequently viewed faces. Faces similar to those seen previously are judged more normal and attractive than they were prior to exposure. Here we show sex-contingent after-effects following adaptation to eye-spacing (experiment 1), facial identity (experiment 2) and masculinity (experiment 3). Viewing faces of one sex with increased eye-spacing and faces of the other sex with decreased eye-spacing simultaneously induced opposite after-effects for male and female faces (assessed by normality judgments). Viewing faces transformed in identity or masculinity increased preferences for novel faces with characteristics similar to those viewed only when the sex of the faces presented in the adaptation phase and in post-adaptation preference tests were congruent. Because after-effects reflect changes in responses of neural populations that code faces, our findings indicate that distinct neural populations code male and female faces.

SUBMITTER: Little AC

PROVIDER: S-EPMC1560190 | biostudies-literature | 2005 Nov

REPOSITORIES: biostudies-literature

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Sex-contingent face after-effects suggest distinct neural populations code male and female faces.

Little Anthony C AC DeBruine Lisa M LM Jones Benedict C BC

Proceedings. Biological sciences 20051101 1578

Exposure to faces biases perceptions of subsequently viewed faces. Faces similar to those seen previously are judged more normal and attractive than they were prior to exposure. Here we show sex-contingent after-effects following adaptation to eye-spacing (experiment 1), facial identity (experiment 2) and masculinity (experiment 3). Viewing faces of one sex with increased eye-spacing and faces of the other sex with decreased eye-spacing simultaneously induced opposite after-effects for male and ...[more]

PMID: 16191641

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Project description:BackgroundChinese bayberry (Myrica rubra Sieb. & Zucc.) is an important subtropical evergreen fruit tree in southern China. Generally dioecious, the female plants are cultivated for fruit and have been studied extensively, but male plants have received very little attention. Knowledge of males may have a major impact on conservation and genetic improvement as well as on breeding. Using 84 polymorphic SSRs, we genotyped 213 M. rubra individuals (99 male individuals, 113 female varieties and 1 monoecious) and compared the difference in genetic diversity between the female and the male populations.ResultsNeighbour-joining cluster analysis separated M. rubra from three related species, and the male from female populations within M. rubra. By structure analysis, 178 M. rubra accessions were assigned to two subpopulations: Male dominated (98) and Female dominated (80). The well-known cultivars 'Biqi' and 'Dongkui', and the landraces 'Fenhong' are derived from three different gene pools. Female population had a slightly higher values of genetic diversity parameters (such as number of alleles and heterozygosity) than the male population, but not significantly different. The SSR loci ZJU062 and ZJU130 showed an empirical Fst value of 0.455 and 0.333, respectively, which are significantly above the 95 % confidence level, indicating that they are outlier loci related to sex separation.ConclusionThe male and female populations of Chinese bayberry have similar genetic diversity in terms of average number of alleles and level of heterozygosity, but were clearly separated by genetic structure analysis due to two markers associated with sex type, ZJU062 and ZJU130. Zhejiang Province China could be the centre of diversity of M. rubra in China, with wide genetic diversity coverage; and the two representative cultivars 'Biqi' and 'Dongkui', and one landrace 'Fenhong' in three female subpopulations. This research provides genetic information on male and female Chinese bayberry and will act as a reference for breeding programs.

Project description:BACKGROUND:Sex-differences in cancer occurrence and mortality are evident across tumor types; men exhibit higher rates of incidence and often poorer responses to treatment. Targeted approaches to the treatment of tumors that account for these sex-differences require the characterization and understanding of the fundamental biological mechanisms that differentiate them. Hepatocellular Carcinoma (HCC) is the second leading cause of cancer death worldwide, with the incidence rapidly rising. HCC exhibits a male-bias in occurrence and mortality, but previous studies have failed to explore the sex-specific dysregulation of gene expression in HCC. METHODS:Here, we characterize the sex-shared and sex-specific regulatory changes in HCC tumors in the TCGA LIHC cohort using combined and sex-stratified differential expression and eQTL analyses. RESULTS:By using a sex-specific differential expression analysis of tumor and tumor-adjacent samples, we uncovered etiologically relevant genes and pathways differentiating male and female HCC. While both sexes exhibited activation of pathways related to apoptosis and cell cycle, males and females differed in the activation of several signaling pathways, with females showing PPAR pathway enrichment while males showed PI3K, PI3K/AKT, FGFR, EGFR, NGF, GF1R, Rap1, DAP12, and IL-2 signaling pathway enrichment. Using eQTL analyses, we discovered germline variants with differential effects on tumor gene expression between the sexes. 24.3% of the discovered eQTLs exhibit differential effects between the sexes, illustrating the substantial role of sex in modifying the effects of eQTLs in HCC. The genes that showed sex-specific dysregulation in tumors and those that harbored a sex-specific eQTL converge in clinically relevant pathways, suggesting that the molecular etiologies of male and female HCC are partially driven by differential genetic effects on gene expression. CONCLUSIONS:Sex-stratified analyses detect sex-specific molecular etiologies of HCC. Overall, our results provide new insight into the role of inherited genetic regulation of transcription in modulating sex-differences in HCC etiology and provide a framework for future studies on sex-biased cancers.

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Sex-contingent face after-effects suggest distinct neural populations code male and female faces.

Publications

Sex-contingent face after-effects suggest distinct neural populations code male and female faces.

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