C. Mcarthur et al., SALIVARY PROLINE-RICH PROTEINS IN MAMMALS - ROLES IN ORAL HOMEOSTASISAND COUNTERACTING DIETARY TANNIN, Journal of chemical ecology, 21(6), 1995, pp. 663-691
We review information on the structure of proline-rich proteins (PRPs)
, their various functions related to oral homeostasis and dietary tann
in, and the structural basis of these functions. Considerations of the
multifunctional nature of these salivary proteins helps explain both
the subtle and large variations found in structure and secretion rates
both within individuals and between species. We propose that the ance
stral function of PRPs is in maintaining oral homeostasis and that cou
nteracting dietary tannins by binding with them is a derived function.
PRPs are effective in oral homeostasis at low secretion levels, where
as counteracting tannin depends on high secretion levels. In the dieta
ry habits ranging from carnivores through omnivores to exclusively pla
nt-eaters, the dietary nitrogen level is progressively reduced, and pl
ant allelo-chemical intake, including tannins, increases. We suggest t
hat during this evolution from meat-eater to plant-eater, there was so
me point in omnivory at which selective pressure from nitrogen limitat
ions, arising from a low nitrogen/high tannin diet, became sufficientl
y great for the evolution of increased secretion level and diversifica
tion of PRPs for dealing with tannin. If this hypothesis is correct, c
arnivorous mammals should secrete low levels of PRPs for oral homeosta
sis, but should never secrete high levels, unless they are secondarily
carnivorous. Omnivores consuming a diet of very little animal tissue
but higher levels of tannin-containing foliage or fruit should general
ly have the capacity to produce high levels of salivary PRPs. Browsers
and frugivores should also produce high levels of PRPs, but grazers m
ay have reduced secretion rates depending on the antiquity of the diet
ary habit. This hypothesis is consistent with the limited information
available on the abundance, type, and distribution of PRPs in mammals.
Studies are suggested which would test the functional and evolutionar
y arguments presented.