Developmental expression of the creatine kinase isozyme system of Xenopus: maternally derived CK-IV isoform persists far beyond the degradation of its maternal mRNA and into the zygotic expression period

Development ◽  
1990 ◽  
Vol 108 (3) ◽  
pp. 507-514
Author(s):  
J. Robert ◽  
J. Wolff ◽  
H. Jijakli ◽  
J.D. Graf ◽  
F. Karch ◽  
...  
Keyword(s):  
Creatine Kinase ◽  
Differential Expression ◽  
Early Development ◽  
Developmental Expression ◽  
Developmental Profile ◽  
Maternal Mrna ◽  
Skeletal Musculature ◽  
Adult Pattern ◽  
Specific Manner ◽  
Isozyme System

The differential expression of the multilocus CK isozyme system throughout development of the two Xenopus species X. laevis and X. borealis was investigated. A cDNA containing the nearly complete coding sequence of the CK-IV subunit of X. laevis was isolated and sequenced. Early development of X. laevis proceeds with a stock of maternally derived CK-IV/IV isozyme. While the mRNA declines rapidly after fertilization and disappears before neurulation, maternal CK-IV/IV isozyme is active far beyond the onset of zygotic expression and is still detectable when tadpoles start feeding. Zygotic expression of CK-IV begins after neurulation, at stage 22/24, and seems to start simultaneously with that of another gene, CK-III. Modulation in the expression of these two genes and the appearance of two other isoforms, the CK-I and CK-II/III isozymes, take place during development in a tissue-specific manner. During metamorphosis, the CK phenotypes of eyes and skeletal musculature undergo additional changes. The final adult pattern only appears several weeks after metamorphosis. The presumed orthologous CK isozymes of X. borealis show a developmental profile similar to that of X. laevis, except that CK-II/II is equally present in oocytes and during early development, in addition to CK-IV/IV isozyme. These results show that the expression of each of the four CK genes of Xenopus is under differential developmental control.

scholarly journals Tentacle Morphological Variation Coincides with Differential Expression of Toxins in Sea Anemones

Toxins ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 452
Author(s):  
Lauren M. Ashwood ◽  
Michela L. Mitchell ◽  
Bruno Madio ◽  
David A. Hurwood ◽  
Glenn F. King ◽  
...  
Keyword(s):  
Differential Expression ◽  
Morphological Variation ◽  
Expression Profiles ◽  
The Body ◽  
Sea Anemones ◽  
Tissue Specific ◽  
Venom Composition ◽  
Specific Manner ◽  
Branched Structures ◽  
Morphological Variants

Phylum Cnidaria is an ancient venomous group defined by the presence of cnidae, specialised organelles that serve as venom delivery systems. The distribution of cnidae across the body plan is linked to regionalisation of venom production, with tissue-specific venom composition observed in multiple actiniarian species. In this study, we assess whether morphological variants of tentacles are associated with distinct toxin expression profiles and investigate the functional significance of specialised tentacular structures. Using five sea anemone species, we analysed differential expression of toxin-like transcripts and found that expression levels differ significantly across tentacular structures when substantial morphological variation is present. Therefore, the differential expression of toxin genes is associated with morphological variation of tentacular structures in a tissue-specific manner. Furthermore, the unique toxin profile of spherical tentacular structures in families Aliciidae and Thalassianthidae indicate that vesicles and nematospheres may function to protect branched structures that host a large number of photosynthetic symbionts. Thus, hosting zooxanthellae may account for the tentacle-specific toxin expression profiles observed in the current study. Overall, specialised tentacular structures serve unique ecological roles and, in order to fulfil their functions, they possess distinct venom cocktails.

Synthesis and phosphorylation of uvomorulin during mouse early development

Development ◽  
1992 ◽  
Vol 115 (1) ◽  
pp. 313-318 ◽  
Author(s):  
M. Sefton ◽  
M.H. Johnson ◽  
L. Clayton
Keyword(s):  
Cell Adhesion ◽  
Early Development ◽  
Adhesion Molecule ◽  
Cell Adhesion Molecule ◽  
Blastocyst Stage ◽  
Embryonic Stage ◽  
Cell Stage ◽  
Mouse Oocytes ◽  
Maternal Mrna ◽  
Embryonic Genome

The cell adhesion molecule, uvomorulin, is synthesised in both the 135 × 10(3) M(r) precursor and 120 × 10(3) M(r) mature forms on maternal mRNA templates in unfertilized and newly fertilized mouse oocytes. Synthesis on maternal message ceases during the 2-cell stage to resume later on mRNA encoded presumptively by the embryonic genome. Uvomorulin is detectable by immunoblotting at all stages upto the blastocyst stage, but shows variations in its total amount and processing with embryonic stage. Whilst only trace levels of phosphorylated uvomorulin are detectable in early and late 4-cell embryos, uvomorulin in 8-cell embryos is phosphorylated.

Differential expression and cellular localization of somatolactin-1 and -2 during early development in the gilthead sea bream

2003 ◽  
Vol 132 (1) ◽  
pp. 77-87 ◽  
Author(s):  
M. Javier Herrero-Turrión ◽  
Raquel E. Rodrı́guez ◽  
Almudena Velasco ◽  
José Aijón ◽  
Juan M. Lara
Keyword(s):  
Differential Expression ◽  
Early Development ◽  
Cellular Localization ◽  
Gilthead Sea Bream ◽  
Sea Bream

Analysis of transcriptional regulation of the s38 chorion gene of Drosophila by P element-mediated transformation

Development ◽  
1984 ◽  
Vol 83 (Supplement) ◽  
pp. 137-146
Author(s):  
Laura Kalfayan ◽  
Barbara Wakimoto ◽  
Allan Spradling
Keyword(s):  
Transcriptional Regulation ◽  
P Element ◽  
Developmental Expression ◽  
Developmental Profile ◽  
E Coli ◽  
Flanking Sequences ◽  
Dna Fragment ◽  
P Element Transformation ◽  
Lac Z

Transcriptional regulation of the s38 chorion gene was studied using P element-mediated germline transformation. A 5·27 kb DNA fragment containing the s38 gene and 5′- and 3′-flanking sequences, was tested for its ability to be transcribed with correct developmental specificity. Five single-insert transformed lines were generated by microinjection of this DNA fragment cloned into a marked P element transformation vector. In each line, the transformed gene was transcribed according to the precise developmental pattern followed by the native s38 gene. The 1·3 kb at the 5′ end of this tested fragment was fused to the E. coli lac z gene. This fragment was also capable of initiating transcription of E. coli lac z RNA with the developmental profile of the native s38 gene. In vitro deletion studies are underway to determine which sequences in the 1·3 kb fragment are necessary for regulating the developmental expression of the gene.

Maternal mRNA Expression in Early Development: Regulation at the 3' End

Enzyme ◽  
1990 ◽  
Vol 44 (1-4) ◽  
pp. 129-146 ◽  
Author(s):  
Jeannie Paris ◽  
L. Lynn McGrew ◽  
Joel D. Richter
Keyword(s):  
Mrna Expression ◽  
Early Development ◽  
Maternal Mrna ◽  
Development Regulation

Ontogeny of the Electroreceptive System of The Platypus.

1998 ◽  
Vol 20 (2) ◽  
pp. 309
Author(s):  
P.R. Manger ◽  
R. Collins ◽  
J.D. Pettigrew
Keyword(s):  
Histological Examination ◽  
Developmental Stages ◽  
Developmental Profile ◽  
Adult Pattern ◽  
Poorly Differentiated ◽  
Sensory Structures

A series of developmental stages of the platypus were examined in order to obtain an anatomical description of the development of the periphery of the electroreceptive system. Putative electroreceptors, composed of modified mucous glands, were observed to appear at I0 days post hatching (p.h.). The typical striped arrangement of peripheral electroreceptors in the platypus was seen at 12 days p.h. The arrangement of the stripes was modified during development with a range of additions and divisions of stripes occurring until the adult pattern is obtained, approximately 6 months p.h. After appearing at 10 days p.h. the number of electroreceptors increases rapidly until sometime between 24 and 28 days p.h. when there is massive death of electroreceptors, the number present at 28 days p.h. being 60% of the number present at 24 days p.h. This massive death of receptors is coincident with the appearance of other sensory structures in the epidermis of the bill skin, the push-rod mechanoreceptors and the sensory serous glands. Histological examination of a range of developmental stages demonstrated poorly differentiated innervation at 28 days p.h. which became differentiated and reached the adult configuration between 11 weeks p.h. and 6 months p.h. Lamination of the cells lining the duct of the electroreceptors showed a similar developmental profile. This study indicates that the electroreceptive system of the developing platypus is not functional, in a similar manner to the adult, until around the time the platypus leaves the nesting burrow. However, the system may be functional in the developing platypus, and speculatively may be used in the location o f the mammary region for suckling.

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