Australian lungfish (Neoceratodus forsteri): a missing link in the evolution of complementary side biases for predator avoidance and prey capture.

Side biases in behavior, reflecting lateral specializations of the brain, are widespread amongst vertebrates. We studied laterality in the Australian lungfish (Neoceratodus forsteri) to gain insight into the evolution of the complementary specializations of predator avoidance (right hemisphere) and foraging behavior (left hemisphere). Because N. forsteri is the closest extant ancestor of the first land-dwelling vertebrates, knowledge of laterality in this species should provide a missing link in the transition from fish to tetrapods. Predator escape responses were elicited by generating pressure waves and a significant bias for C-start responses to the left side was found. This bias was unaffected by activity levels that change according to a diurnal cycle: activity is higher in the dark phase than the light phase. A complementary bias to turn to the right side was found during feeding behavior. This pattern of opposite-side specializations matches that known for fish, anurans, reptiles, birds and, as some evidence indicates, also mammals. Hence, we conclude that it is a homologous pattern of lateralization that evolved in early aquatic vertebrates and was retained as they made the transition to land-dwelling tetrapods.

Thyroid hormone deiodinases revisited: insights from lungfish: a review.

In vertebrates, hormones released from the thyroid gland travel in the circulation to target tissues where they may be processed by deiodinating enzymes into more active or inactive iodothyronines. In mammals, there are three deiodinating enzymes described. Type1 (D1), which primarily occurs in the liver, converts reverse T3 into T2 for clearance. It also converts T4 into T3. This production of T3 is believed to contribute to the bulk of circulating T3 in mammals. The type2 (D2) enzyme may be found in many other tissues where it converts T4 to T3, which is then transferred to the receptors in the nucleus of the same cell, i.e. does not contribute to the circulating T3. The type3 (D3) enzyme converts T3 into T2. The expression of the genes for these three enzymes and/or the activity of the enzymes have been studied in several non-mammalian groups of vertebrates. From agnathans to birds, D2 and D3 appear to occur universally, with the possible exception of squamate reptiles (lack D2?). D1 has not been found in amphibians, lungfish or agnathans. All three enzymes are selenoproteins, in which a selenocysteine is found in the active centre. The nucleotide code for translation of a selenocysteine is UGA, which under normal circumstances is a stop codon. In order for UGA to code for selenocysteine, there must be a SECIS element in the 3'UTR of the mRNA. Any disruption of the SECIS will result in a truncated protein in the region of its active centre. It is suggested that such alternative splicing may be a mode of altering the expression of deiodinases in particular tissues to change the response of such tissues to thyroid hormones under differing circumstances such as stages of development.

The seasonal reproductive cycle of a marsupial, Antechinus stuartii: effects of oral administration of melatonin.

Antechinus stuartii is a small marsupial with a brief, highly synchronised mating period believed to be controlled by the rate of change of photoperiod. Two experiments were performed to explore aspects of photoperiodic control of the seasonal cycle. In the first experiment the pineal hormone, melatonin, administered in the drinking water from the winter solstice, changed the normal response of A. stuartii to increasing rate of change of photoperiod. Melatonin administration shifted the induction of estrus in the females from the first week of August (controls) to an earlier time of mid-July and the consequent pouch changes associated with pregnancy and pseudo-pregnancy were also shifted by the same length of time. Post-mating decline and consequent death of males were also accelerated. In the second experiment melatonin was administered from the autumnal equinox, and this experimental protocol resulted in a desynchronisation of reproductive events. Melatonin administration desynchronised the female reproductive cycle, such that the mating period was extended to eight weeks, instead of the two weeks displayed by control females. Pouch changes and birth of young reflected this desynchronisation. Melatonin administration in males resulted in desynchronisation of reproductive parameters. While the normal yearly reproductive cycle was approximated in these males, the high syncronisation of reproductive maturation and male mortality events observed in control males, was not evident in melatonin-treated males. These results indicate that the pineal gland by way of the hormone melatonin is important in the synchronisation of the unusual life history of this marsupial mammal.