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A Kunitz type protease inhibitor related protein is synthesized in Drosophila prepupal salivary glands and released into the moulting fluid during pupation.
- Source :
-
Insect biochemistry and molecular biology [Insect Biochem Mol Biol] 2004 Aug; Vol. 34 (8), pp. 855-69. - Publication Year :
- 2004
-
Abstract
- From the Drosophila virilis late puff region 31C, we microcloned two neighbouring genes, Kil-1 and Kil-2, that encode putative Kunitz serine protease inhibitor like proteins. The Kil-1 gene is expressed exclusively in prepupal salivary glands. Using a size mutant of the KIL-1 protein and MALDI-TOF analysis, we demonstrate that during pupation this protein is released from the prepupal salivary glands into the pupation fluid covering the surface of the pupa. 3-D-structure predictions are consistent with the known crystal structure of the human Kunitz type protease inhibitor 2KNT. This is the first experimental proof for the extracorporal presence of a distinct Drosophila prepupal salivary gland protein. Possible functions of KIL-1 in the context of the control of proteolytic activities in the pupation fluid are discussed.
- Subjects :
- Amino Acid Sequence
Animals
Base Sequence
Cloning, Molecular
Drosophila growth & development
Endopeptidases metabolism
Evolution, Molecular
Genes, Insect genetics
Larva enzymology
Larva genetics
Molecular Sequence Data
Physical Chromosome Mapping
Pupa genetics
Pupa metabolism
Salivary Proteins and Peptides chemistry
Salivary Proteins and Peptides genetics
Sequence Analysis, Protein
Trypsin Inhibitors chemistry
Trypsin Inhibitors genetics
Aprotinin chemistry
Drosophila genetics
Larva metabolism
Salivary Glands growth & development
Salivary Glands metabolism
Salivary Proteins and Peptides metabolism
Trypsin Inhibitors metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0965-1748
- Volume :
- 34
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Insect biochemistry and molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 15262289
- Full Text :
- https://doi.org/10.1016/j.ibmb.2004.05.006