Cyclic development of contact behavior in apes and humans

Nursing and mother-infant distance were observed in three orangutans, two gorillas, one chimpanzee and four humans. All four species showed periods of a recurrence of greater time spent nursing and in contact with the mother. The initial regressive or reattachment period occurred similarly in all four species at between 6–12 months of age. An orangutan observed for two years showed a second period at 19–21 months. Other studies of weight gain in the three ape species coincidently peaked at the same time. When estimated peaks of individuals of each species were summed, the resulting graphs showed a differentiation of species rates of development. Gorillas developed most rapidly, orangutans developed most slowly, while chimpanzees and humans developed within the middle range.     

Antifolding activity of hsp60 couples protein import into the mitochondrial matrix with export to the intermembrane space.

Cytochrome b2 reaches the intermembrane space of mitochondria by transport into the matrix followed by export across the inner membrane. While in the matrix, the protein interacts with hsp60, which arrests its folding prior to export. The bacterial-type export sequence in pre-cytochrome b2 functions by inhibiting the ATP-dependent release of the protein from hsp60. Release for export apparently requires, in addition to ATP, the interaction of the signal sequence with a component of the export machinery in the inner membrane. Export can occur before import is complete provided that a critical length of the polypeptide chain has been translocated into the matrix. Thus, hsp60 combines two activities: catalysis of folding of proteins destined for the matrix, and maintaining proteins in an unfolded state to facilitate their channeling between the machineries for import and export across the inner membrane. Anti-folding signals such as the hydrophobic export sequence in cytochrome b2 may act as switches between these two activities.     

Use of surrogate parental models and age periods in a successful release of hand-reared sandhill cranes

Ten sandhill crane chicks were reared in isolation from humans to prepare them for an experimental wild release. They were imprinted on realistic models using crane brooding calls and were fed by crane-like puppets. Six of the chicks were simultaneously imprinted on a human in a crane costume. The other four chicks were introduced to this surrogate parent at 5–7 days of age. The chicks were fed natural foods by the parent at two wild sites, one of which, the release site, was a staging area for migratory cranes. Observations were made on their behavioral development, including the time spent close to the model or costumed parent and the percentage of time spent foraging. The chicks spent the initial month close to the surrogate parent but moved away more to forage during the second month. The chicks regressed to again spend a great deal of time near the parent during the third and fourth months. They were released during this regressive period by removing the surrogate parent. All five of the released chicks showed increased interest in wild cranes within days of the release and formed a continuous association with wild cranes within 30 days. Four of the five were relocated by telemetry the following spring back in Wisconsin. These young juvenile cranes were excellent candidates for release due to their adaptable nature and their level of social development. The artificial stimuli of the surrogate parent helped the chicks to generalize their attachment to wild cranes. Once with wild cranes they quickly learned additional survival skills.     

Species status of the black howler monkey,Alouatta pigra,of Belize

Small troop sizes which averaged 5.23 members per troop and the early descent of male testes inAlouatta pigra show a marked difference fromA. palliata. These differences strengthenSmith's (1970) observations of morphological differences betweenA. pigra andA. palliata.     

Geographical distribution of the black howler (Alouatta pigra) in Central America

The geographic range of the black howler,Alouatta pigra in Mexico, Guatemala, and Belize was investigated by travelling through and visiting 65 locations within or close to the expected range. The existence of the species was noted through first hand observations or was documented by talking with residents and knowledgeable people in the area. Observations were made on captive animals as well. All sites and probable sites ofA. pigra were noted to be under 1,300 ft in altitude and in areas with a mean annual temperature above 25°C and a mean annual rainfall over 1,000 mm per year. This area coincides with tropical rain forest areas, including both tropical evergreen and semievergreen rain forests.A. pigra was most plentiful in riverine areas which showed flooding for some part of the year. Two areas of possible sympatry withA. palliata were noted. In all cases, the troop sizes ofA. pigra were extremely small, under ten individuals, and infants could easily be sexed, in contrast toA. palliata which is known to occur in troops of 15–18 and is difficult to sex at an early age. Finally, a very gross method for population estimation from searching time emerged from the study.     

Meiotic expression of human ornithine transcarbamylase in the testes of transgenic mice.

In an attempt to use mouse metallothionein-I (mMT-I) regulatory sequences to direct expression of human ornithine transcarbamylase in the liver of transgenic animals, fusion genes joining either 1.6 kilobases or 185 base pairs of the mMT-I regulatory region to the human ornithine transcarbamylase protein-coding sequence were used to produce transgenic mice. In mice carrying the fusion gene with 1.6 kilobases of the mMT-I 5'-flanking sequences, transgene expression was observed in a wide range of tissues, but, unexpectedly, expression in liver was never observed. Surprisingly, in mice carrying the fusion gene regulated by only 185 base pairs of the mMT-I 5'-flanking sequences, the transgene was expressed exclusively in male germ cells during the tetraploid, pachytene stage of meiosis.     

Sorting pathways of mitochondrial inner membrane proteins

Two distinct pathways of sorting and assembly of nuclear-encoded mitochondrial inner membrane proteins are described. In the first pathway, precursor proteins that carry amino-terminal targeting signals are initially translocated via contact sites between both mitochondrial membranes into the mitochondrial matrix. They become proteolytically processed, interact with the 60-kDa heat-shock protein hsp60 in the matrix and are retranslocated to the inner membrane. The sorting of subunit 9 of Neurospora crassa F0-ATPase has been studied as an example. F0 subunit 9 belongs to that class of nuclear-encoded mitochondrial proteins which are evolutionarily derived from a prokaryotic ancestor according to the endosymbiont hypothesis. We suggest that after import into mitochondria, these proteins follow the ancestral sorting and assembly pathways established in prokaryotes (conservative sorting). On the other hand, ADP/ATP carrier was found not to require interaction with hsp60 for import and assembly. This agrees with previous findings that the ADP/ATP carrier possesses non-amino-terminal targeting signals and uses a different import receptor to other mitochondrial precursor proteins. It is proposed that the ADP/ATP carrier represents a class of mitochondrial inner membrane proteins which do not have a prokaryotic equivalent and thus appear to follow a non-conservative sorting pathway.     

GroEL-GroES cycling: ATP and nonnative polypeptide direct alternation of folding-active rings.

The double-ring chaperonin GroEL mediates protein folding in the central cavity of a ring bound by ATP and GroES, but it is unclear how GroEL cycles from one folding-active complex to the next. We observe that hydrolysis of ATP within the cis ring must occur before either nonnative polypeptide or GroES can bind to the trans ring, and this is associated with reorientation of the trans ring apical domains. Subsequently, formation of a new cis-ternary complex proceeds on the open trans ring with polypeptide binding first, which stimulates the ATP-dependent dissociation of the cis complex (by 20- to 50-fold), followed by GroES binding. These results indicate that, in the presence of nonnative protein, GroEL alternates its rings as folding-active cis complexes, expending only one round of seven ATPs per folding cycle.     

Exploring the structural dynamics of the E.coli chaperonin GroEL using translation-libration-screw crystallographic refinement of intermediate states

Large rigid-body domain movements are critical to GroEL-mediated protein folding, especially apical domain elevation and twist associated with the formation of a folding chamber upon binding ATP and co-chaperonin GroES. Here, we have modeled the anisotropic displacements of GroEL domains from various crystallized states, unliganded GroEL, ATPgammaS-bound, ADP-AlFx/GroES-bound, and ADP/GroES bound, using translation-libration-screw (TLS) analysis. Remarkably, the TLS results show that the inherent motions of unliganded GroEL, a polypeptide-accepting state, are biased along the transition pathway that leads to the folding-active state. In the ADP-AlFx/GroES-bound folding-active state the dynamic modes of the apical domains become reoriented and coupled to the motions of bound GroES. The ADP/GroES complex exhibits these same motions, but they are increased in magnitude, potentially reflecting the decreased stability of the complex after nucleotide hydrolysis. Our results have allowed the visualization of the anisotropic molecular motions that link the static conformations previously observed by X-ray crystallography. Application of the same analyses to other macromolecules where rigid body motions occur may give insight into the large scale dynamics critical for function and thus has the potential to extend our fundamental understanding of molecular machines.