Adaptive Profile Versus Adaptive Specialization: Fossils and Gummivory in Early Primate Evolution

Author(s):  
Alfred L. Rosenberger
2008 ◽  
Vol 16 (1) ◽  
pp. 41-56 ◽  
Author(s):  
Hildegard Kehrer-Sawatzki ◽  
David N. Cooper

2009 ◽  
Vol 277 (1684) ◽  
pp. 1011-1020 ◽  
Author(s):  
Chet C. Sherwood ◽  
Mary Ann Raghanti ◽  
Cheryl D. Stimpson ◽  
Muhammad A. Spocter ◽  
Monica Uddin ◽  
...  

Inhibitory interneurons participate in local processing circuits, playing a central role in executive cognitive functions of the prefrontal cortex. Although humans differ from other primates in a number of cognitive domains, it is not currently known whether the interneuron system has changed in the course of primate evolution leading to our species. In this study, we examined the distribution of different interneuron subtypes in the prefrontal cortex of anthropoid primates as revealed by immunohistochemistry against the calcium-binding proteins calbindin, calretinin and parvalbumin. In addition, we tested whether genes involved in the specification, differentiation and migration of interneurons show evidence of positive selection in the evolution of humans. Our findings demonstrate that cellular distributions of interneuron subtypes in human prefrontal cortex are similar to other anthropoid primates and can be explained by general scaling rules. Furthermore, genes underlying interneuron development are highly conserved at the amino acid level in primate evolution. Taken together, these results suggest that the prefrontal cortex in humans retains a similar inhibitory circuitry to that in closely related primates, even though it performs functional operations that are unique to our species. Thus, it is likely that other significant modifications to the connectivity and molecular biology of the prefrontal cortex were overlaid on this conserved interneuron architecture in the course of human evolution.


1999 ◽  
Vol 16 (2) ◽  
pp. 357-362
Author(s):  
Heui-Soo Kim ◽  
Catharine Winstanley ◽  
Rekha V. Wadekar ◽  
Osamu Takenaka ◽  
Fusako Mitsunaga ◽  
...  

2011 ◽  
Vol 68 (3) ◽  
pp. 499-506 ◽  
Author(s):  
W. Stewart Grant ◽  
Susan E. Merkouris ◽  
Gordon H. Kruse ◽  
Lisa W. Seeb

AbstractGrant, W. S., Merkouris, S. E., Kruse, G. H., and Seeb, L. W. 2011. Low allozyme heterozygosity in North Pacific and Bering Sea populations of red king crab (Paralithodes camtschaticus): adaptive specialization, population bottleneck, or metapopulation structure? – ICES Journal of Marine Science, 68: . Populations of red king crab in the North Pacific and Bering Sea have declined in response to ocean-climate shifts and to harvesting. An understanding of how populations are geographically structured is important to the management of these depressed resources. Here, the Mendelian variability at 38 enzyme-encoding loci was surveyed in 27 samples (n = 2427) from 18 general locations. Sample heterozygosities were low, averaging HE = 0.015 among samples. Weak genetic structure was detected among three groups of populations, the Bering Sea, central Gulf of Alaska, and Southeast Alaska, but without significant isolation by distance among populations. A sample from Adak Island in the western Aleutians was genetically different from the remaining samples. The lack of differentiation among populations within regions may, in part, be due to post-glacial expansions and a lack of migration-drift equilibrium and to limited statistical power imposed by low levels of polymorphism. Departures from neutrality may reflect the effects of both selective and historical factors. The low allozyme diversity in red king crab may, in part, be attributable to adaptive specialization, background selection, ice-age population bottlenecks, or metapopulation dynamics in a climatically unstable North Pacific.


2010 ◽  
Vol 185 (9) ◽  
pp. 5360-5368 ◽  
Author(s):  
Wilfred W. Raymond ◽  
Neil N. Trivedi ◽  
Anastasia Makarova ◽  
Manisha Ray ◽  
Charles S. Craik ◽  
...  

Science News ◽  
1994 ◽  
Vol 145 (16) ◽  
pp. 245
Author(s):  
B. Bower
Keyword(s):  

1990 ◽  
Vol 10 (6) ◽  
pp. 2513-2520
Author(s):  
L C Samuelson ◽  
K Wiebauer ◽  
C M Snow ◽  
M H Meisler

We have analyzed the junction regions of inserted elements within the human amylase gene complex. This complex contains five genes which are expressed at high levels either in the pancreas or in the parotid gland. The proximal 5'-flanking regions of these genes contain two inserted elements. A gamma-actin pseudogene is located at a position 200 base pairs upstream of the first coding exon. All of the amylase genes contain this insert. The subsequent insertion of an endogenous retrovirus interrupted the gamma-actin pseudogene within its 3'-untranslated region. Nucleotide sequence analysis of the inserted elements associated with each of the five human amylase genes has revealed a series of molecular events during the recent history of this gene family. The data indicate that the entire gene family was generated during primate evolution from one ancestral gene copy and that the retroviral insertion activated a cryptic promoter.


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