PMID- 9144202 OWN - NLM STAT- MEDLINE DCOM- 19970605 LR - 20190524 IS - 0027-8424 (Print) IS - 1091-6490 (Electronic) IS - 0027-8424 (Linking) VI - 94 IP - 10 DP - 1997 May 13 TI - Cooperative functions of the reaper and head involution defective genes in the programmed cell death of Drosophila central nervous system midline cells. PG - 5131-6 AB - In Drosophila, the chromosomal region 75C1-2 contains at least three genes, reaper (rpr), head involution defective (hid), and grim, that have important functions in the activation of programmed cell death. To better understand how cells are killed by these genes, we have utilized a well defined set of embryonic central nervous system midline cells that normally exhibit a specific pattern of glial cell death. In this study we show that both rpr and hid are expressed in dying midline cells and that the normal pattern of midline cell death requires the function of multiple genes in the 75C1-2 interval. We also utilized the P[UAS]/P[Gal4] system to target expression of rpr and hid to midline cells. Targeted expression of rpr or hid alone was not sufficient to induce ectopic midline cell death. However, expression of both rpr and hid together rapidly induced ectopic midline cell death that resulted in axon scaffold defects characteristic of mutants with abnormal midline cell development. Midline-targeted expression of the baculovirus p35 protein, a caspase inhibitor, blocked both normal and ectopic rpr- and hid-induced cell death. Taken together, our results suggest that rpr and hid are expressed together and cooperate to induce programmed cell death during development of the central nervous system midline. FAU - Zhou, L AU - Zhou L AD - Biology Department, University of Massachusetts at Amherst, Amherst, MA 01003, USA. FAU - Schnitzler, A AU - Schnitzler A FAU - Agapite, J AU - Agapite J FAU - Schwartz, L M AU - Schwartz LM FAU - Steller, H AU - Steller H FAU - Nambu, J R AU - Nambu JR LA - eng GR - R01 GM040458/GM/NIGMS NIH HHS/United States GR - AG55118/AG/NIA NIH HHS/United States GR - GM40458/GM/NIGMS NIH HHS/United States GR - NS32251/NS/NINDS NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Proc Natl Acad Sci U S A JT - Proceedings of the National Academy of Sciences of the United States of America JID - 7505876 RN - 0 (Drosophila Proteins) RN - 0 (Peptides) RN - 0 (Recombinant Proteins) RN - 0 (rpr protein, Drosophila) RN - EC 3.2.1.23 (beta-Galactosidase) SB - IM MH - Animals MH - Apoptosis MH - Crosses, Genetic MH - Drosophila/cytology/genetics/*physiology MH - *Drosophila Proteins MH - Embryo, Nonmammalian/cytology/physiology MH - *Gene Expression Regulation, Developmental MH - *Genes, Insect/*genetics/physiology MH - Multigene Family MH - Nervous System/cytology/embryology MH - *Nervous System Physiological Phenomena MH - Neuroglia/cytology/physiology MH - Peptide Biosynthesis MH - Peptides/*genetics MH - Recombinant Proteins/biosynthesis MH - beta-Galactosidase/biosynthesis PMC - PMC24643 EDAT- 1997/05/13 00:00 MHDA- 1997/05/13 00:01 PMCR- 1997/11/13 CRDT- 1997/05/13 00:00 PHST- 1997/05/13 00:00 [pubmed] PHST- 1997/05/13 00:01 [medline] PHST- 1997/05/13 00:00 [entrez] PHST- 1997/11/13 00:00 [pmc-release] AID - 0895 [pii] AID - 10.1073/pnas.94.10.5131 [doi] PST - ppublish SO - Proc Natl Acad Sci U S A. 1997 May 13;94(10):5131-6. doi: 10.1073/pnas.94.10.5131.