4.4 Article

The proprotein convertase amontillado (amon) is required during Drosophila pupal development

期刊

DEVELOPMENTAL BIOLOGY
卷 333, 期 1, 页码 48-56

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2009.06.021

关键词

Prohormone convertase; PC2; Pupal development; Metamorphosis; Ecdysis

资金

  1. National Institutes of Health [GM53681]
  2. National Science Foundation [IOS-0823472]
  3. ARCS Foundation Fellowship
  4. American Association of UniversityWomen Educational Foundation Dissertation Fellowship
  5. National Institutes of Health Training [GM07103]
  6. University of Georgia
  7. Direct For Biological Sciences
  8. Division Of Integrative Organismal Systems [0823472] Funding Source: National Science Foundation

向作者/读者索取更多资源

Peptide hormones governing many developmental processes are generated via endoproteolysis of inactive precursor molecules by a family of subtilisin-like proprotein convertases (SPCs). We previously identified mutations in the Drosophila amontillado (amon) gene, a homolog of the vertebrate neuroendocrine-specific Prohormone Convertase 2 (PC2) gene, and showed that amon is required during embryogenesis, early larval development, and larval molting. Here, we de. ne amon requirements during later developmental stages using a conditional rescue system and find that amon is required during pupal development for head eversion, leg and wing disc extension, and abdominal differentiation. Immuno-localization experiments show that amon protein is expressed in a subset of central nervous system cells but does not co-localize with peptide hormones known to elicit molting behavior, suggesting the involvement of novel regulatory peptides in this process. The amon protein is expressed in neuronal cells that innervate the corpus allatum and corpora cardiaca of the ring gland, an endocrine organ which is the release site for many key hormonal signals. Expression of amon in a subset of these cell types using the GAL4/UAS system in an amon mutant background partially rescues larval molting and growth. Our results show that amon is required for pupal development and identify a subset of neuronal cell types in which amon function is sufficient to rescue developmental progression and growth defects shown by amon mutants. The results are consistent with a model that the amon protein acts to proteolytically process a diverse suite of peptide hormones that coordinate larval and pupal growth and development. (C) 2009 Elsevier Inc. All rights reserved.

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