Role of the Neural Crest in Vertebrate Development and Evolution by Nicole Le Douarin, March 2008 - Part 1: The Quail Chick Marker System and Its Use to Study the Ontogeny of the Neural Crest (24:45)

SciVee ◽  
2008 ◽  
2021 ◽  
pp. 105971232110306
Author(s):  
Vincenzo Raimondi

Genetic reductionism is increasingly seen as a severely limited approach to understanding living systems. The Neo-Darwinian explanatory framework tends to overlook the role of the organism for an understanding of development and evolution. In the current fast-changing theoretical landscape, the autopoietic approach provides conceptual distinctions and tools that may contribute to building an alternative framework. In this article, I examine the implications of the theories of autopoiesis and natural drift for an organism-centered view of evolution. By shifting the attention from genes to ontogenetic organism-niche configurations and their transformations over generations, this approach presents a compelling perspective on the role of organismal behavior in guiding phylogenetic drift.


2006 ◽  
Vol 235 (10) ◽  
pp. 2722-2735 ◽  
Author(s):  
Binnur Eroglu ◽  
Guanghu Wang ◽  
Naxin Tu ◽  
Xutong Sun ◽  
Nahid F. Mivechi

2002 ◽  
Vol 251 (1) ◽  
pp. 157-166 ◽  
Author(s):  
Lazaros Kochilas ◽  
Sandra Merscher-Gomez ◽  
Min Min Lu ◽  
Vijaya Potluri ◽  
Jun Liao ◽  
...  

Development ◽  
1988 ◽  
Vol 102 (2) ◽  
pp. 301-310 ◽  
Author(s):  
R.M. Langille ◽  
B.K. Hall

Lamprey embryos were obtained by artificial fertilization to ascertain the contributions made by the neural crest to the head skeleton. Early-neurula-stage embryos of Petromyzon marinus were subjected to neural crest extirpation along the anterior half from one of seven zones, raised to a larval stage at which control larvae exhibit well-developed skeletons and analysed by light microscopy for any abnormalities to the cranial and visceral skeleton. The removal of premigratory neural crest at the level of the anterior prosencephalon (zone I) and at the level of somites 6 to 8 (zone VII) had no effect on skeletal development. However, the extirpation of neural crest from the intervening regions was positively correlated with deletions/reductions to the trabeculae (basicranial elements) and to the branchial arches (viscerocranial elements). Alterations to the trabeculae (16/27 cases, or 59%) occurred only after extirpation of zones II-V (corresponding to the posterior prosencephalon to midrhombencephalon) while alterations to the branchial arches (21/28 cases, or 75%) occurred only after removal of neural crest from zones III-VI (corresponding to the mesencephalon to the level of the fifth somite). Furthermore, the first three branchial arches were correlated in a majority of cases with neural crest from zone III, the next two arches with zones IV, V and VI and the last two arches with zone VI. Organs that develop within or adjacent to the area of neural crest extirpation such as the brain, notochord and lateral mesodermal derivatives were not affected. Parachordals were never altered by the operations nor were there any discernible changes to developing mucocartilage or to the prechondrogenic otic capsule. The contributions of the neural crest to the petromyzonid head skeleton described herein are compared with the roles of neural crest in the development of cranial and visceral skeletal elements in other vertebrates. The importance of these findings to the current hypothesis of the phylogeny of the vertebrate skeleton and the central role of the neural crest in vertebrate cephalization is discussed.


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