Identification of four Drosophila allatostatins as the cognate ligands for the Drosophila orphan receptor DAR-2.

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Identification of four Drosophila allatostatins as the cognate ligands for the Drosophila orphan receptor DAR-2. / Lenz, C; Williamson, M; Hansen, G N; Grimmelikhuijzen, C J.

In: Biochemical and Biophysical Research Communications, Vol. 286, No. 5, 2001, p. 1117-22.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Lenz, C, Williamson, M, Hansen, GN & Grimmelikhuijzen, CJ 2001, 'Identification of four Drosophila allatostatins as the cognate ligands for the Drosophila orphan receptor DAR-2.', Biochemical and Biophysical Research Communications, vol. 286, no. 5, pp. 1117-22. https://doi.org/10.1006/bbrc.2001.5475

APA

Lenz, C., Williamson, M., Hansen, G. N., & Grimmelikhuijzen, C. J. (2001). Identification of four Drosophila allatostatins as the cognate ligands for the Drosophila orphan receptor DAR-2. Biochemical and Biophysical Research Communications, 286(5), 1117-22. https://doi.org/10.1006/bbrc.2001.5475

Vancouver

Lenz C, Williamson M, Hansen GN, Grimmelikhuijzen CJ. Identification of four Drosophila allatostatins as the cognate ligands for the Drosophila orphan receptor DAR-2. Biochemical and Biophysical Research Communications. 2001;286(5):1117-22. https://doi.org/10.1006/bbrc.2001.5475

Author

Lenz, C ; Williamson, M ; Hansen, G N ; Grimmelikhuijzen, C J. / Identification of four Drosophila allatostatins as the cognate ligands for the Drosophila orphan receptor DAR-2. In: Biochemical and Biophysical Research Communications. 2001 ; Vol. 286, No. 5. pp. 1117-22.

Bibtex

@article{18df3300ec2811dcbee902004c4f4f50,
title = "Identification of four Drosophila allatostatins as the cognate ligands for the Drosophila orphan receptor DAR-2.",
abstract = "The allatostatins are generally inhibitory insect neuropeptides. The Drosophila orphan receptor DAR-2 is a G-protein-coupled receptor, having 47% amino acid residue identity with another Drosophila receptor, DAR-1 (which is also called dros. GPCR, or DGR) that was previously shown to be the receptor for an intrinsic Drosophila A-type (cockroach-type) allatostatin. Here, we have permanently expressed DAR-2 in CHO cells and found that it is the cognate receptor for four Drosophila A-type allatostatins, the drostatins-A1 to -A4. Of all the drostatins, drostatin-A4 (Thr-Thr-Arg-Pro-Gln-Pro-Phe-Asn-Phe-Gly-Leu-NH(2)) is the most effective in causing a second messenger cascade (measured as bioluminescence; threshold, 10(-9) M; EC(50), 10(-8) M), whereas the others are less effective and about equally potent (EC(50), 8 x 10(-8) M). Northern blots showed that the DAR-2 gene is expressed in embryos, larvae, pupae, and adult flies. In adult flies, the receptor is more strongly expressed in the thorax/abdomen than in the head parts, suggesting that DAR-2 is a gut receptor. This is confirmed by Northern blots from 3rd instar larvae, showing that the DAR-2 gene is mainly expressed in the gut and only very weakly in the brain. The Drosophila larval gut also contains about 20-30 endocrine cells, expressing the gene for the drostatins-A1 to -A4. We suggest, therefore, that DAR-2 mediates an allatostatin (drostatin)-induced inhibition of gut motility. This is the first report on the permanent and functional expression of a Drosophila gut neurohormone receptor.",
author = "C Lenz and M Williamson and Hansen, {G N} and Grimmelikhuijzen, {C J}",
note = "Keywords: Amino Acid Sequence; Animals; Blotting, Northern; Brain; CHO Cells; Cloning, Molecular; Cricetinae; Dose-Response Relationship, Drug; Drosophila; Drosophila Proteins; Gene Expression Regulation, Developmental; Humans; In Situ Hybridization; Insect Proteins; Intestines; Kinetics; Ligands; Luminescent Measurements; Molecular Sequence Data; Neuropeptides; Protein Binding; Receptors, Cell Surface; Receptors, G-Protein-Coupled; Receptors, Neuropeptide; Time Factors",
year = "2001",
doi = "10.1006/bbrc.2001.5475",
language = "English",
volume = "286",
pages = "1117--22",
journal = "Biochemical and Biophysical Research Communications",
issn = "0006-291X",
publisher = "Elsevier",
number = "5",

}

RIS

TY - JOUR

T1 - Identification of four Drosophila allatostatins as the cognate ligands for the Drosophila orphan receptor DAR-2.

AU - Lenz, C

AU - Williamson, M

AU - Hansen, G N

AU - Grimmelikhuijzen, C J

N1 - Keywords: Amino Acid Sequence; Animals; Blotting, Northern; Brain; CHO Cells; Cloning, Molecular; Cricetinae; Dose-Response Relationship, Drug; Drosophila; Drosophila Proteins; Gene Expression Regulation, Developmental; Humans; In Situ Hybridization; Insect Proteins; Intestines; Kinetics; Ligands; Luminescent Measurements; Molecular Sequence Data; Neuropeptides; Protein Binding; Receptors, Cell Surface; Receptors, G-Protein-Coupled; Receptors, Neuropeptide; Time Factors

PY - 2001

Y1 - 2001

N2 - The allatostatins are generally inhibitory insect neuropeptides. The Drosophila orphan receptor DAR-2 is a G-protein-coupled receptor, having 47% amino acid residue identity with another Drosophila receptor, DAR-1 (which is also called dros. GPCR, or DGR) that was previously shown to be the receptor for an intrinsic Drosophila A-type (cockroach-type) allatostatin. Here, we have permanently expressed DAR-2 in CHO cells and found that it is the cognate receptor for four Drosophila A-type allatostatins, the drostatins-A1 to -A4. Of all the drostatins, drostatin-A4 (Thr-Thr-Arg-Pro-Gln-Pro-Phe-Asn-Phe-Gly-Leu-NH(2)) is the most effective in causing a second messenger cascade (measured as bioluminescence; threshold, 10(-9) M; EC(50), 10(-8) M), whereas the others are less effective and about equally potent (EC(50), 8 x 10(-8) M). Northern blots showed that the DAR-2 gene is expressed in embryos, larvae, pupae, and adult flies. In adult flies, the receptor is more strongly expressed in the thorax/abdomen than in the head parts, suggesting that DAR-2 is a gut receptor. This is confirmed by Northern blots from 3rd instar larvae, showing that the DAR-2 gene is mainly expressed in the gut and only very weakly in the brain. The Drosophila larval gut also contains about 20-30 endocrine cells, expressing the gene for the drostatins-A1 to -A4. We suggest, therefore, that DAR-2 mediates an allatostatin (drostatin)-induced inhibition of gut motility. This is the first report on the permanent and functional expression of a Drosophila gut neurohormone receptor.

AB - The allatostatins are generally inhibitory insect neuropeptides. The Drosophila orphan receptor DAR-2 is a G-protein-coupled receptor, having 47% amino acid residue identity with another Drosophila receptor, DAR-1 (which is also called dros. GPCR, or DGR) that was previously shown to be the receptor for an intrinsic Drosophila A-type (cockroach-type) allatostatin. Here, we have permanently expressed DAR-2 in CHO cells and found that it is the cognate receptor for four Drosophila A-type allatostatins, the drostatins-A1 to -A4. Of all the drostatins, drostatin-A4 (Thr-Thr-Arg-Pro-Gln-Pro-Phe-Asn-Phe-Gly-Leu-NH(2)) is the most effective in causing a second messenger cascade (measured as bioluminescence; threshold, 10(-9) M; EC(50), 10(-8) M), whereas the others are less effective and about equally potent (EC(50), 8 x 10(-8) M). Northern blots showed that the DAR-2 gene is expressed in embryos, larvae, pupae, and adult flies. In adult flies, the receptor is more strongly expressed in the thorax/abdomen than in the head parts, suggesting that DAR-2 is a gut receptor. This is confirmed by Northern blots from 3rd instar larvae, showing that the DAR-2 gene is mainly expressed in the gut and only very weakly in the brain. The Drosophila larval gut also contains about 20-30 endocrine cells, expressing the gene for the drostatins-A1 to -A4. We suggest, therefore, that DAR-2 mediates an allatostatin (drostatin)-induced inhibition of gut motility. This is the first report on the permanent and functional expression of a Drosophila gut neurohormone receptor.

U2 - 10.1006/bbrc.2001.5475

DO - 10.1006/bbrc.2001.5475

M3 - Journal article

C2 - 11527415

VL - 286

SP - 1117

EP - 1122

JO - Biochemical and Biophysical Research Communications

JF - Biochemical and Biophysical Research Communications

SN - 0006-291X

IS - 5

ER -

ID: 3045981