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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Development genes and evolution 198 (1989), S. 129-136 
    ISSN: 1432-041X
    Keywords: Bioluminescence ; Polar lobe ; Spiralian development
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The light emitting photocytes ofChaetopterus variopedatus larvae are bilaterally situated within the ectoderm of the post-trochal region. Their histological appearance is similar to that of the adult photocytes. The larval photocytes contain a large quantity of membranous secretory vesicles (photosomes), which probably contain the photoluminescent protein. The two-cellChaetopterus embryo contains a small AB and a large CD blastomere. Previous studies have shown that only the “larvae” resulting from isolated CD blastomeres are able to luminesce. Consistent with these findings, morphologically distinct photocytes are only found in the CD larvae. The removal of the small polar lobe that forms during first cleavage leads to the production of a “larva” that is unable to produce light. All delobed larvae contain morphologically distinct photocytes, which are identical to those in normal larvae except they appear to contain only a small quantity of photosomes. Experimental equalization of first cleavage leads to the production of a double embryo. While photocytes are found in both of the duplicated post-trochal regions, usually only one of these is capable of emitting luminescence. Apparently, the highly localized vagetal material (determinants) responsible for functional light emission is distributed to both halves in only a few cases when first cleavage is experimentally “equalized”. These results indicate that the determinative action of the polar lobe is not required for the formation of the photocytes themselves, but rather for their ability to function as emitters of light. The determinants in the polar lobe ofChaetopterus may control some aspect of the photoluminescence reaction itself, such as the production of the photoprotein.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-041X
    Keywords: Determination/intermediate ; filament/gene ; expression/in situ ; hybridization/chick ; embryo/germ layers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Using in situ hybridization we show that a chick type II cytokeratin (CKsel) is differentially expressed within the developing ectoderm, mesoderm, and endoderm as early as the time of germ layer formation. CKsel expression demarcates specific regions that in many instances can be correlated with distinct presumptive developmental fates or potencies. In the epiblast of definitive streak stage embryos, CKsel hybridization is detected only in regions destined to form extraembryonic ectoderm. After this stage expression occurs within embryonic ectoderm but is largely restricted to regions that will form epidermis. It is not detected in presumptive neural ectoderm or in most regions of head ectoderm. The area of non-expression of CKsel in head ectoderm delineates ectoderm which has a strong bias for lens formation, and gives rise not only to lenses but to other placodally derived structures such as the nasal epithelium and the otic vesicles. In the developing mesoderm, CKsel transcripts become restricted to regions of lateral plate and extraembryonic mesodermal tissues at later stages. CKsel is expressed throughout the developing endoderm except in the region of the presumptive foregut roof. There is a unifying pattern to the expression of CKsel transcripts in all three germ layers: it is expressed in more lateral areas which generally have more ventral fates, beginning at the time of germ layer formation and indicating the existence of medial/lateral boundaries early in development.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-041X
    Keywords: Determination ; Polar lobe ; Unequal cleavage ; Spiralians
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The inequality of the first cleavage division of the Chætopterus embryo is caused by the production of a small polar lobe and the internal shifting of the first cleavage spindle. This division produces a two-celled embryo containing a small AB and a large CD blastomere. These blastomeres have different morphogenetic potentials. Only the larvae resulting from isolated CD blastomeres are able to form bioluminescent photocytes, eyes and lateral hooked bristles. The removal of the polar lobe during first cleavage does not have a great effect on development. These lobeless embryos display a normal pattern of cleavages through the time of mesentoblast formation. The resulting larvae are essentially normal, however they do not form functional photocytes. If the CD cell is isolated after the removal of the first polar lobe, the resulting larva is virtually identical to those formed by the intact CD cell except it lacks the photocyte cells. These results indicate that two separate pathways are involved in the segregation of developmental or morphogenetic potential which takes place during first cleavage. One set of factors, which are necessary for photocyte formation, are associated with the first polar lobe. Other factors that are necessary for the formation of the eyes and lateral hooked bristles are segregated by the unequal cleavage which results from an internal shifting of the cleavage spindle. The removal of a large portion of the vegetal region of the embryo during first cleavage leads to the production of larvae which display a decreased ability to form eyes and lateral hooked bristles. These embryos frequently display an abnormal pattern of cleavages. They do not form the primary somatoblast or the mesentoblast. These results indicate that the vegetal region of the CD cell of Chætopterus is analogous to polar lobes which have been studied in other species, and is therefore important in the specification of the D quadrant. These features of the first cleavage of Chætopterus are a combination of those displayed by forms with direct unequal cleavage and other forms which cleave unequally through the production of large polar lobes. The significance of these findings is discussed relative to the origins of these different types of unequal cleavage.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-041X
    Keywords: Dorsoventral polarity ; Egg organization ; Spiral cleavage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The egg of the polychaete Chætopterus, like many spiralian embryos, undergoes unequal cleavage during the first two cell divisions following fertilization. The first cleavage gives rise to a large CD blastomere and a smaller AB blastomere. At second cleavage the CD blastomere divides asymmetrically, forming a large D blastomere and a smaller C blastomere while the AB cell divides to give rise to the two smaller blastomeres, A and B, which are virtually identical in size. As in many of the other spiralians which have been studied, the A, B, C, and D blastomeres give rise to characteristic portions of the larval body plan. It has been shown in these related forms that the D blastomere derivatives are necessary for the production of various structures derived from the remaining three quadrants, as well as in organizing the overall symmetry properties of the embryo. If Chætopterus embryos are compressed underneath a coverslip at the appropriate stage of development prior to first cleavage (the “pear stage”) some of the embryos divide to form two equal sized blastomeres. Each of the two cells in equalized embryos appears to develop as a normal CD blastomere often dividing to generate a four-celled embryo with two C and two D blastomeres opposite one another (CDCD embryos). These embryos often grow up to form larvae which have duplicated structures. We investigated the role of the early cleavage program in the production of double larvae by staining individual blastomeres of normal and equalized embryos with Nile blue sulfate. Our results reveal that previous descriptions of the symmetry properties of twinned larvae are incorrect. Twins are not true Janus larvae of the duplicitus cruciata form but are organized along a single axis. The two halves face one another along a plane of mirror symmetry, each one fused to the other at their ventral surface just above a single, common, fused mouth. Furthermore, the median plane of the two fused heads is the same as that of the two trunks. These labeling studies indicate that cells derived from both of the two C blastomeres in compressed embyos contribute to the formation of similar structures in both halves of the double larva. The two C quadrants within the double embryos each can give rise to two eyes, and the plane of mirror symmetry between the two halves of the double embryo as mentioned above corresponds to a plane running through the two C blastomeres in the fourcelled CDCD embryo. These findings indicate that the two D quadrants in these double embryos interact to organize the development of the double embryo in a coordinating manner. Both D quadrants, therefore, appear to be inductively active within the CDCD double embryos. These results are discussed in view of various hypotheses which have been proposed to explain the phenomenon of twinning in spiralians.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Hydrobiologia 383 (1998), S. 137-137 
    ISSN: 1573-5117
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Because the embryos of polyclad turbellarians exhibit the ancestral features of quartet spiral cleavage and a trochophore-type larva, knowledge of polyclad development is crucial to understanding the evolution of development in the Spiralia. Surprisingly polyclads have been the subject of few developmental investigations, and experiments have been done only on the embryos of Hoploplana inquilina (see Boyer, 1995). However interpretation of the results of this work has been handicapped by the lack of a complete cell lineage of the embryo. Recently Henry et al. (1995) have shown that the quadrant fates of four-cell stage Hoploplana embryos are essentially identical to those of the higher Spiralia. The present study follows the cell lineage from the eight-cell stage through the fourth quartet. The first three quartets of micromeres form primarily ectoderm, including the nervous system. Mesoderm comes from second and fourth quartet blastomeres, with 2b giving rise to circular muscles and 4d to longitudinal muscles and mesenchyme. The remainder of the fourth quartet apparently serves as nutrient reserves for the developing embryo. This work demonstrates a striking similarity between the cell lineages of polyclad and higher spiralian embryos. It also confirms that there are both ectodermal (2b) and endodermal (4d) contributions to the mesoderm in primitive spiralians and supports the concept that the dual origin of mesoderm represents the ancestral condition.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Hydrobiologia 402 (1999), S. 255-265 
    ISSN: 1573-5117
    Keywords: evolution ; spiral cleavage ; Spiralia ; cell lineage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract It is clear that the spiralian developmental program represents a highly flexible platform for the generation of diverse larval and adult body plans. The widespread occurrence of this pattern of early development attests to its tremendous evolutionary success. Despite the large degree of conservation in the spiral cleavage pattern and other basic aspects of early development, changes in cell fate maps and in the mechanisms of blastomere specification have arisen. While we have learned a great deal about this mode of development, a number of important questions remain to be answered. To what extent do these conditions apply to the lesser studied spiralian phyla? What constraints have led to the preservation of the early spiral cleavage program? How has this developmental program been adapted for the construction of the various spiralian body plans (e.g. the segmental body plans of annelids or to the potential secondary loss of segmentation)? Are most changes associated with the elaboration of these different larval and adult body plans restricted to the late period of development? What molecular/genetic processes underlie this developmental program? Clearly, the spiralian phyla represent an important group of organisms for further studies on development and evolution.
    Type of Medium: Electronic Resource
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