Hepatic expression of cytochrome P450 enzymes in non-human primate species.

Cytochromes P450 (P450) largely remain to be characterized in great apes. Comparative immunochemical detection of drug metabolizing forms of P450s 1A, 2A, 2B, 2C, 2D, 2E, 2J, 3A, 4A, and 4F in liver microsomes from chimpanzees, gorillas, orangutans, gibbons, cynomolgus and rhesus macaques, and common marmosets were carried out.

Genetic comparisons yield insight into the evolution of enamel thickness during human evolution.

Enamel thickness varies substantially among extant hominoids and is a key trait with significance for interpreting dietary adaptation, life history trajectory, and phylogenetic relationships. There is a strong link in humans between enamel formation and mutations in the exons of the four genes that code for the enamel matrix proteins and the associated protease. The evolution of thick enamel in humans may have included changes in the regulation of these genes during tooth development. The cis-regulatory region in the 5' flank (upstream non-coding region) of MMP20, which codes for enamelysin, the predominant protease active during enamel secretion, has previously been shown to be under strong positive selection in the lineages leading to both humans and chimpanzees. Here we examine evidence for positive selection in the 5' flank and 3' flank of AMELX, AMBN, ENAM, and MMP20. We contrast the human sequence changes with other hominoids (chimpanzees, gorillas, orangutans, gibbons) and rhesus macaques (outgroup), a sample comprising a range of enamel thickness. We find no evidence for positive selection in the protein-coding regions of any of these genes. In contrast, we find strong evidence for positive selection in the 5' flank region of MMP20 and ENAM along the lineage leading to humans, and in both the 5' flank and 3' flank regions of MMP20 along the lineage leading to chimpanzees. We also identify putative transcription factor binding sites overlapping some of the species-specific nucleotide sites and we refine which sections of the up- and downstream putative regulatory regions are most likely to harbor important changes. These non-coding changes and their potential for differential regulation by transcription factors known to regulate tooth development may offer insight into the mechanisms that allow for rapid evolutionary changes in enamel thickness across closely-related species, and contribute to our understanding of the enamel phenotype in hominoids.

Hormonal correlates of paternal care differences in the Hylobatidae.

Only one of the 15 species of monogamous hylobatids, the siamang (Symphalangus syndactylus), demonstrates direct paternal care in the form of infant-carrying, providing a unique model for examining hormonal correlates of paternal care differences between siamangs and gibbons. We used behavioral data and fecal hormone analysis to investigate (1) differences in monthly percent father-infant proximity in relation to monthly fecal androgen metabolite concentrations from infant birth to the late postpartum period between siamangs and gibbons, (2) the pattern of change in fecal androgen and fecal estrogen metabolite concentrations during the 8-week peripartum period between siamangs and gibbons, and (3) the change in mean fecal glucocorticoid metabolite concentrations at 1-month postpartum from individual baseline between siamangs and gibbons. Father-infant proximity increased as androgen concentrations decreased over the postpartum period in siamangs but not in gibbons. Androgen concentrations increased around birth in siamangs during the 8-week peripartum period, but exhibited a decreasing trend around birth in gibbons. Estrogen concentrations increased from pre- to postpartum in siamangs during the 8-week peripartum period, but exhibited a decreasing trend from pre- to postpartum in gibbons. The difference in mean glucocorticoid metabolite concentrations from baseline was greater in siamangs than gibbons. Our data suggest a relationship between specific steroid hormone patterns and differences in paternal care among the hylobatids, warranting further investigation of such proximate mechanisms.

Comparative energetics of primate fetal growth.

Among the primates, Homo sapiens has evolved a life history which includes long gestation, relatively slow growth to reproductive maturity, and large body size. While the slow growth rate may be linked to the energetic demands of having a large brain, there are other important morphological and physiological linkages that may be adaptive, including the development of significant fat stores with which to buffer against episodic and periodic energetic stress. In this comparative analysis of the energetic burden of pregnancy among primates (including humans), the daily energy investment in the development of neonatal tissue is modeled. During pregnancy, larger primates, notably the Hominidae, invest a smaller proportion of their maternal daily nonmaintenance energy budget in fetal tissue with increasing energy budget, allowing diverse adaptations, including foraging strategies which include folivory and mixed patterns of food getting, and meat consumption. Humans have a similar proportion of maternal daily nonmaintenance energy budget invested in fetal tissue with increasing energy budget to other apes and have a diet which is of much higher quality than predicted for body size and metabolic needs. The combination of high diet quality and low proportion of maternal daily nonmaintenance energy budget invested in fetal tissue allows greater brain size relative to body weight at birth compared with all other primates, apart from chimpanzees, and higher birthweight and body fatness at birth for a given body size than other primate species.