Characterization of RNA species synthesized during early development of sea urchins

1965 ◽  
Vol 14 (1) ◽  
pp. 195-213 ◽  
Author(s):  
Donald G. Comb ◽  
Solomon Katz ◽  
Richard Branda ◽  
Charles J. Pinzino
Author(s):  
D. F. Blake ◽  
L. F. Allard ◽  
D. R. Peacor

Echinodermata is a phylum of marine invertebrates which has been extant since Cambrian time (c.a. 500 m.y. before the present). Modern examples of echinoderms include sea urchins, sea stars, and sea lilies (crinoids). The endoskeletons of echinoderms are composed of plates or ossicles (Fig. 1) which are with few exceptions, porous, single crystals of high-magnesian calcite. Despite their single crystal nature, fracture surfaces do not exhibit the near-perfect {10.4} cleavage characteristic of inorganic calcite. This paradoxical mix of biogenic and inorganic features has prompted much recent work on echinoderm skeletal crystallography. Furthermore, fossil echinoderm hard parts comprise a volumetrically significant portion of some marine limestones sequences. The ultrastructural and microchemical characterization of modern skeletal material should lend insight into: 1). The nature of the biogenic processes involved, for example, the relationship of Mg heterogeneity to morphological and structural features in modern echinoderm material, and 2). The nature of the diagenetic changes undergone by their ancient, fossilized counterparts. In this study, high resolution TEM (HRTEM), high voltage TEM (HVTEM), and STEM microanalysis are used to characterize tha ultrastructural and microchemical composition of skeletal elements of the modern crinoid Neocrinus blakei.


2016 ◽  
Author(s):  
Eric M. Erkenbrack ◽  
Eric H. Davidson

AbstractDevelopmental gene regulatory networks (GRNs) are assemblages of gene regulatory interactions that direct ontogeny of animal body plans. Studies of GRNs operating in early development of euechinoid sea urchins has revealed that little appreciable change has occurred since their divergence approximately 90 million years ago (mya). These observations suggest that strong conservation of GRN architecture has been maintained in early development of the sea urchin lineage. To test whether this is true for all sea urchins, comparative analyses of echinoid taxa that diverged deeper in geological time must be conducted. Recent studies highlighted extensive divergence of skeletogenic mesoderm specification in the sister clade of euechinoids, the cidaroids, suggesting that comparative analyses of cidaroid GRN architecture may confer a greater understanding of the evolutionary dynamics of developmental GRNs. Here, we report spatiotemporal patterning of 55 regulatory genes and perturbation analyses of key regulatory genes involved in euechinoid oral-aboral patterning of non-skeletogenic mesodermal and ectodermal domains in early development of the cidaroid Eucidaris tribuloides. Our results indicate that developmental GRNs directing mesodermal and ectodermal specification have undergone marked alterations since the divergence of cidaroids and euechinoids. Notably, statistical and clustering analyses of echinoid temporal gene expression datasets indicate that regulation of mesodermal genes has diverged more markedly than regulation of ectodermal genes. Although research on indirect-developing euechinoid sea urchins suggests strong conservation of GRN circuitry during early embryogenesis, this study indicates that since the divergence of cidaroids and euechinoids developmental GRNs have undergone significant divergence.


1990 ◽  
Vol 142 (2) ◽  
pp. 486-488 ◽  
Author(s):  
Margaret Truschel Peeler ◽  
Leslie Kelso-Winemiller ◽  
Ming-Fan Wu ◽  
James K. Skipper ◽  
Matthew M. Winkler

2002 ◽  
Vol 14 (5) ◽  
pp. 269-277 ◽  
Author(s):  
Giuseppe Testa ◽  
Riccardo Caccia ◽  
Francesca Tilesi ◽  
Gian Soressi ◽  
Andrea Mazzucato
Keyword(s):  

Development ◽  
1999 ◽  
Vol 126 (19) ◽  
pp. 4305-4315 ◽  
Author(s):  
Y. Cinnamon ◽  
N. Kahane ◽  
C. Kalcheim

We have previously found that the myotome is formed by a first wave of pioneer cells generated along the medial epithelial somite and a second wave emanating from the dorsomedial lip (DML), rostral and caudal edges of the dermomyotome (Kahane, N., Cinnamon, Y. and Kalcheim, C. (1998a) Mech. Dev. 74, 59–73; Kahane, N., Cinnamon, Y. and Kalcheim, C. (1998b) Development 125, 4259–4271). In this study, we have addressed the development and precise fate of the ventrolateral lip (VLL) in non-limb regions of the axis. To this end, fluorescent vital dyes were iontophoretically injected in the center of the VLL and the translocation of labeled cells was followed by confocal microscopy. VLL-derived cells colonized the ventrolateral portion of the myotome. This occurred following an early longitudinal cell translocation along the medial boundary until reaching the rostral or caudal dermomyotome lips from which fibers emerged into the myotome. Thus, the behavior of VLL cells parallels that of their DML counterparts which colonize the opposite, dorsomedial portion of the myotome. To precisely understand the way the myotome expands, we addressed the early generation of hypaxial intercostal muscles. We found that intercostal muscles were formed by VLL-derived fibers that intermingled with fibers emerging from the ventrolateral aspect of both rostral and caudal edges of the dermomyotome. Notably, hypaxial intercostal muscles also contained pioneer myofibers (first wave) showing for the first time that lateral myotome-derived muscles contain a fundamental component of fibers generated in the medial domain of the somite. In addition, we show that during myotome growth and evolution into muscle, second-wave myofibers progressively intercalate between the pioneer fibers, suggesting a constant mode of myotomal expansion in its dorsomedial to ventrolateral extent. This further suggests that specific hypaxial muscles develop following a consistent ventral expansion of a ‘compound myotome’ into the somatopleure.


Author(s):  
Keith Stewart Thomson

The Amphibia has been one of the most important animal groups for the study of developmental biology, and a huge descriptive and experimental literature has accumulated over the years. While sea urchins, molluscs, and nematodes, and more recently, Drosophila, have each become an important vehicle for the study of different aspects of development, the Amphibia and chordates in general have been especially important as the vehicle for the study of inductive regulative mechanisms. The early development of all chordates is marked by two revolutions in the control of early pattern formation: dorsalization at the blastula stage and gastrulation—primary induction caused by the “organizer” —which was studied in great detail in Amphibia by Spemann and his coworkers and continues to be the subject of intense scrutiny. The early phases of development in Amphibia exemplify rather well some of the problems in discovering the causal processes in development, whether in the egg, at fertilization, in the blastula, or in gastrulation itself. The short discussion of early development in Amphibia that follows is meant to exemplify rather than catalogue these questions. The oocyte in amphibians is radially symmetrical. A first axis of symmetry is established between a more heavily pigmented animal hemisphere and a less pigmented vegetal hemisphere. Before fertilization the egg is covered with a transparent vitelline membrane. When fertilization occurs, the vitelline membrane lifts from the surface of the egg and the egg is then free to rotate inside it so that the animal hemisphere lies uppermost and the vegetal hemisphere is lowermost. This rotation is apparently a response to gravity, which means that the vegetal hemisphere is heavier, almost certainly a result of the concentration of more and larger yolk granules in the vegetal hemisphere. Therefore, if the egg rotates to a new orientation with the yolk down and the animal hemisphere up, it must be the case that at this point the yolk and other egg contents are not free to be redistributed within the egg but are secured in place. The animal vegetal axis now marks the future anteroposterior axis of the embryo.


1996 ◽  
Vol 30 (10) ◽  
pp. 2508-2511 ◽  
Author(s):  
Mutsuyasu Nakajima ◽  
Takahiro Ogura ◽  
Yoshiyuki Kusama ◽  
Noriyuki Iwabuchi ◽  
Taichi Imawaka ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document