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  • Embryogenesis  (2)
  • Bean-shaped accessory gland  (1)
  • 1
    ISSN: 1432-041X
    Keywords: Key words BHR39 ; BmFTZ-F1 ; Embryogenesis ; Diapause ; Bombyx mori
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  In the silkworm, Bombyx mori, the 5’-upstream region of the sorbitol dehydrogenase (SDH) gene contains nucleotide sequences that might be recognized and bound by steroid hormone receptors such as Drosophila hormone receptor 39 (DHR39) and Fushi tarazu transcription factor 1 (FTZ-F1). As a first trial to find out regulator(s) involved in gene expression for SDH in Bombyx eggs, we have cloned a cDNA encoding a Bombyx homolog (BHR39) of DHR39, and examined levels of mRNA expressions for BHR39 and Bombyx FTZ-F1 (BmFTZ-F1) during the entire embryonic development and diapause. During embryonic development of non-diapause eggs, mRNA expression for BmFTZ-F1, but not for BHR39, was shown to occur in parallel with that for SDH, although such a parallelism was not found at the termination of diapause, when SDH mRNA was expressed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-041X
    Keywords: Key words Cyclin ; Embryogenesis ; Insect ; Diapause ; Bombyx mori
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  To understand the molecular mechanism of G2-arrest of cell division in embryonic diapause of the silkworm, Bombyx mori, we have cloned a cDNA encoding a Bombyx homolog of B-type cyclin. Levels of Bm cyclin-B mRNA were examined during diapause stage and early embryogenesis. The results showed that this G2-arrest did not always correspond to lowered transcriptional levels of cyclin-B, and that the mRNA accumulated in oocytes began to be degraded during the first hour after oviposition, i.e. the first meiosis, suggesting that the penetration of sperm triggered the degradation of maternal cyclin-B mRNA.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-136X
    Keywords: Trehalase ; Bean-shaped accessory gland ; Spermatophore ; Male mealworm beetle ; Tenebrio molitor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Trehalase from the bean-shaped accessory glands of the male mealworm beetle, Tenebrio molitor, was purified by acid treatment, with subsequent chromatography on columns of DEAE-cellulofine and Sephacryl S-300. The molecular masses of the native and the denatured forms were estimated to be 43 and 62 kDa by gel filtration and SDS-PAGE, respectively, an indication that the trehalase may be composed of a single polypeptide. The optimum pH of the reaction catalyzed by trehalase was 5.6–5.8. The K m for trehalose was 4.4 mmol·l−1. Immunohistochemical experiments with trehalase-specific antiserum showed that the enzyme was localized in one specific type of secretory cell in the bean-shaped accessory gland epithelium and within the semisolid secretory mass that was a precursor to the wall of spermatophore. SDS-PAGE and immunoblotting analysis revealed the presence of a polypeptide of about 62 kDa in the spermatophore, Immunohistochemical observations showed that the trehalase was located at the outgrowth in the anterior portion of the spermatophore. When a fresh spermatophore was immersed in phosphate-buffered saline it discharged sperm in the same manner as in the bursa copulatrix of the female. Before the rupture of the expanded bulb of the spermatophore, almost all of the trehalase had dissolved in the phosphate-buffered saline. The addition of validoxylamine A to the saline, a specific inhibitor of trehalase, did not affect the expansion and evacuation of the spermatophore. These results demonstrate that trehalase, synthesized by a specific type of secretory cell in the bean-shaped accessory gland epithelium, is actively passed into the lumen of the bean-shaped accessory gland and then incorporated into the spermatophore. Trehalase appears to be one of the structural proteins of the spermatophore, although the possibility can not yet be completely ruled out that the trehalase-trehalose system functions for the nourishment and/or activation of the sperm in the bursa copulatrix of the female.
    Type of Medium: Electronic Resource
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