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Genetic and molecular analysis of maternal information in region 32 of Drosophila melanogaster

1991; Wiley; Volume: 28; Issue: 3 Linguagem: Inglês

10.1002/mrd.1080280314

1098-2795

C. Malva, Franco Graziani, Valeria Cavaliere, Andrea Manzi, Angela Tino,

Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Molecular Reproduction and DevelopmentVolume 28, Issue 3 p. 307-317 Review ArticleFree Access Genetic and molecular analysis of maternal information in region 32 of Drosophila melanogaster Carla Malva, Corresponding Author Carla Malva International Institute of Genetics and Biophysics, CNR, Naples, ItalyInternational Institute of Genetics and Biophysics, CNR, Via Marconi 10, 80125 Naples, ItalySearch for more papers by this authorFranco Graziani, Franco Graziani International Institute of Genetics and Biophysics, CNR, Naples, ItalySearch for more papers by this authorValeria Cavaliere, Valeria Cavaliere International Institute of Genetics and Biophysics, CNR, Naples, ItalySearch for more papers by this authorAndrea Manzi, Andrea Manzi International Institute of Genetics and Biophysics, CNR, Naples, ItalySearch for more papers by this authorAngela Tino, Angela Tino International Institute of Genetics and Biophysics, CNR, Naples, ItalySearch for more papers by this author Carla Malva, Corresponding Author Carla Malva International Institute of Genetics and Biophysics, CNR, Naples, ItalyInternational Institute of Genetics and Biophysics, CNR, Via Marconi 10, 80125 Naples, ItalySearch for more papers by this authorFranco Graziani, Franco Graziani International Institute of Genetics and Biophysics, CNR, Naples, ItalySearch for more papers by this authorValeria Cavaliere, Valeria Cavaliere International Institute of Genetics and Biophysics, CNR, Naples, ItalySearch for more papers by this authorAndrea Manzi, Andrea Manzi International Institute of Genetics and Biophysics, CNR, Naples, ItalySearch for more papers by this authorAngela Tino, Angela Tino International Institute of Genetics and Biophysics, CNR, Naples, ItalySearch for more papers by this author First published: March 1991 https://doi.org/10.1002/mrd.1080280314Citations: 6AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References Bansel R, Pferiffer SE (1985): Developmental expression of 2′-3-cyclic nucleotide 3′-phosphohydrolase in dissociated fetal rat brain cultures and rat brain. J Neurosci Res 14: 21–34. Barnet T, Pachi C, Gergen JP, Wensink PC (1980): The isolation and characterization of Drosophila yolk protein genes. Cell 21: 729–736. Bellen HJ, O'Kane CJ, Wilson C, Grossniklaus U, Pearson RK, Gehring W (1989): P-element-mediated enhancer detection: A versatile method to study development in Drosophila. Genes Dev 3: 1288–1300. Bingham PM, Chapman CH (1986): Evidence that white-blood is a novel type of temperature-sensitive mutation resulting from temperature-dependent effects of a transposon insertion on formation of white transcript. EMBO J 5: 3343–3351. Brennan MD, Weiner AJ, Goralsky TJ, Mahowald AP (1982): The follicle cells are a major site of vitellogenin synthesis in D. melanogaster. Dev Biol 89: 225–236. Burke T, Waring GL, Popodi E, Minoo P (1987): Characterization and sequence of follicle cells genes selectively expressed during vitelline membrane formation in Drosophila. Dev Biol 124: 441–450. Coleman AW, Maguire MJ, Coleman JR (1981): Mithramycin and 4-6-diamidino-2-phenylindole DNA staining for fluorescence microspectro photometric measurement of DNA in nuclei, plastids and virus particles. J Histochem Cytochem 29: 959–964. Ephrussi B, Herold JL (1945): Studies of eye pigments of Drosophila. II. Effect of temperature on the red and brown pigments in the mutant blood. Genetics 30: 62–70. Erdelyi M, Szabad J (1989): Isolation and characterization of dominant female sterile mutations of D. melanogaster. I. Mutations on the third chromosome. Genetics 122: 111–127. Fargnoli J, Waring GL (1982): Identification of vitelline membrane proteins in D. melanogaster. Dev Biol 92: 306–314. Foe VF, Alberts B (1983): Studies of nuclear and cytoplasmic behavior during the five mitotic cycles that precede gastrulation in Drosophila embryogenesis. J Cell Sci 61: 31–70. Gans M, Audit C, Masson M (1975): Isolation and characterization of sex-linked female sterile mutants in D. melanogaster. Genetics 81: 683–704. Gigliotti S, De Ponti L, Raftl F, Manzi A, Graziani F, Malva C, (1986): Isolation of an oocyte specific gene from region 32 of the second chromosome of D. melanogaster. Genetics 113 s: s32. Gigliotti S, Graziani F, De Ponti L, Rafti F, Manzi A, Lavorgna G, Gargiulo G, Malva C (1989): Sex, tissue and stage specific expression of a vitelline membrane protein gene from region 32 of the second chromosome of D. melanogaster. Dev Genet 10: 33–41. Graziani F, Rafti F, Lavorgna G, Gigliotti S, Manzi A, Malva C (1986): Isolation of a putative vitelline membrane gene from the 32 region of the second chromosome of D. melanogaster. Eur J Cell Biol 22: s5. Graziani F, Vicari L, Boncinelli E, Malva C, Manzi A, Mariani C (1981): Selective replication of rDNA repeats after the loss of the abnormal oocyte phenotype in Drosophila melanogaster. Proc Natl Acad Sci USA 78: 7662–7664. Grossniklaus U, Bellen HJ, Wilson C, Gehring W (1989): P-elementmediated enhancer detection applied to the study of oogenesis in Drosophila. Development 107: 189–200. Hafen E, Levine M, Garber RL, Gehring WJ (1983): An improved in situ hybridization method for the detection of cellular RNAs in Drosophila tissue sections and its application for localizing transcripts of the homeotic Antennapedia gene complex. EMBO J 2: 617–623. Illmensee K (1973): The potentialities of transplanted early gastrulanuclei of D. melanogaster: production of their image descendant by germ line transplantation. Wilhelm Roux Arch 191: 191–201. Illmensee K, Mahowald AP, Loomis MR (1976): The ontogeny of germ plasm during oogenesis in Drosophila. Dev Biol 49: 40–65. Ingham PW (1988): The molecular genetics of embryonic pattern formation in Drosophila. Nature 335: 25–34. King RC (1970): Ovarian Development in Drosophila melanogaster. New York: Academic Press. King RC, Mohler J (1975): The genetic analysis of oogenesis in D. melanogaster. In R. C. King (ed): Handbook of Genetics, Vol 3. New York: Plenum Press, pp 757–757. Komitopoulou K, Gans M, Margaritis LH, Kafatos F, Masson M (1983): Isolation and characterization of sex-linked female-sterile mutants in D. melanogaster with special attention to eggshell mutants. Genetics 105: 897–920. Konrad KD, Engstrom L, Perrimon N, Mahowald AP (1985): Genetic analysis of oogenesis and the role of maternal gene expression in early development. In L. W. Browder (ed): Developmental Biology, Vol 1. Oogenesis. New York: Plenum Press, pp 577–577. Krider HM, Levine BI (1975): Studies on the mutation abnormal oocyte and its interaction with the ribosomal DNA of Drosophila melanogaster. Genetics 81: 501–513. Krider HM, Yedvobnik B, Levine BI (1979): The effect of abo phenotypic expression on ribosomal DNA instability in Drosophila melanogaster. Genetics 92: 879–889. Lavorgna G, Malva C, Manzi A, Gigliotti S, Graziani F (1989): The abnormal oocyte phenotype is correlated with the presence of the blood transposon in D. melanogaster. Genetics 123: 485–494. Lin MS, Coming DE, Alfi OS (1977): Optical studies of the interaction of 4′-6′ diamidino-2-phenylindole with DNA and Metaphase chromosomes. Chromosoma 60: 15–25. Lindsley D, Grell EH (1968): Genetic variation of Drosophila melanogaster. Carneige Inst. Wash. Publ. 627. Mahowald AP (1962): Fine structure of pole cells and polar granules in D. melanogaster. J Exp Zool 151: 201–221. Mahowald AP, Kambysellis MP (1980): Oogenesis. In M. Ashburner, T. R. F. Wright (eds): The Genetics and Biology of Drosophila, “Vol 2d.” New York: Academic Press, pp 141–141. Malva C, La Bella T, Manzi A, Salzano G, Lavorgna G, De Ponti L, Graziani F (1985): Maternal and zygotic interaction between the abnormal oocyte mutation and the sc4 inversion in D. melanogaster. Genetics 111: 487–494. Manzi A, Graziani F, La Bella T, Gargiulo G, Rafti F, Malva C (1986): Changes in abo phenotypic expression without increase of rDNA. Mol Gen Genet 205: 366–371. Mariani BD, Lingappa JR, Kafatos FC (1987): Temporal regulation in development: Negative and positive cis regulators dictate the precise timing of expression of a Drosophila chorion gene. Proc Natl Acad Sci USA 85: 3029–3033. Mindrinos MN, Scherer LJ, Garcini FJ, Kwan H, Jacobs KA, Petri WH (1985): Isolation and chromosomal localization of putative vitelline membrane genes in D. melanogaster. EMBO J 4: 147–153. Mitsialis SA, Spoerel N, Leviten M, Kafatos FC (1987): A short 5-flanking DNA region is sufficient for developmentally correct expression of moth chorion genes in Drosophila. Proc Natl Acad Sci USA 84: 7987–7991. Mohler JD (1977): Developmental genetics of the Drosophila egg. I. Identification of 50 sex linked cistrons with maternal effect on embryonic development. Genetics 85: 259–272. Nusslein-Volhard C (1977): Genetic analysis of pattern formation in the embryo of Drosophila melanogaster. Characterization of the maternal effect mutant bicaudal. Wilhelm Roux Arch 183: 249–268. Nusslein-Volhard C, Frohnhofer HG, Lehmann R, (1987): Determination of anteroposterior polarity in Drosophila. Science 238: 1675–1681. Nusslein-Volhard C, Wieschaus E (1980): Mutations affecting segment number and polarity in D. melanogaster. Nature 287: 795–801. O'Kane CJ, Gehring WJ (1987): Detection “in situ” of genomic regulatory elements in Drosophila. Proc Natl Acad Sci USA 84: 9123–9127. Orr WC, Galanopoulos VK, Romano CP, Kafatos F (1989): A female sterile screen of D. melanogaster X chromosome using hybrid disgenesis: Identification and characterization of egg morfology mutants. Genetics 122: 847–858. Parks S, Spradling A (1987): Spatially regulated expression of chorion genes during Drosophila oogenesis. Genes Dev 1: 497–509. Parry DM, Sandler L (1974): The genetic identification of a heterochromatic segment on the X chromosome of Drosophila melanogaster. Genetics 77: 535–539. Perrimon N (1984): Clonal analysis of dominant female sterile germline-dependent mutations in D. melanogaster. Genetics 108: 927–939. Perrimon N, Gans M (1983): Clonal analysis of the tissue specificity of recessive female sterile mutations of D. melanogaster using a dominant female sterile mutation, Fs(1)K1237. Dev Biol 100: 365–378. Perrimon N, Mohler D, Engstrom L, Mahowald AP (1986): X-linked female sterile loci in D. melanogaster. Genetics 113: 695–712. Petri WH, Wyman AR, Kafatos FC (1976): Specific protein synthesis in cellular differentiation III. The eggshell proteins of D. melanogaster and their program of synthesis. Dev Biol 49: 185–199. Pimpinelli S, Sullivan W, Prout M, Sandler L (1985): On biological functions mapping to the heterochromatin of Drosophila melanogaster. Genetics 109: 701–724. Popodi E, Minoo P, Burke T, Waring GL (1988): Organization and expression of a second chromosome follicle cell gene cluster in Drosophila. Dev Biol 127: 248–256. Ritossa F, Atwood FC, Spiegelman S (1966): A molecular explanation of the bobbed mutants of Drosophila as partial deficiencies of ribosomal RNA. Genetics 54: 819–834. Roth S, Stein D, Nusslein-Volhard C (1989): A gradient of nuclear localization of the dorsal protein determines dorsoventral pattern in the Drosophila embryo. Cell 59: 1189–1202. Rubin GM, Spradling AC (1982): Genetic transformation of Drosophila with transposable element vectors. Science 218: 348–353. Sandler L (1970): The regulation of sex-chromosome heterochromatic activity by an autosomal gene in Drosophila melanogaster. Genetics 64: 481–493. Sandler L (1975): Studies on the genetic control of heterochromatin in Drosophila melanogaster. Isr J Med Sci 11: 1124–1134. Sandler L (1977): Evidence for a set of closely linked autosomal genes that interact with sex chromosome heterochromatin in Drosophila melanogaster. Genetics 86: 567–582. Scherer LJ, Harris DH, Petri WH (1988): Drosophila vitelline membrane genes contain a 114 base pair region of highly conserved coding sequence. Dev Biol 130: 786–788. Schupbach T (1987): Germ line and soma cooperate during oogenesis to establish the dorsoventral pattern of egg shell and embryo in D. melanogaster. Cell 49: 699–707. Schupbach T, Wieschaus E (1986): Maternal-effect mutations altering the anterior-posterior pattern of Drosophila embryo. Wilhelm Roux Arch 195: 302–317. Schupbach T, Wieschaus E (1989): Female sterile mutation on the second chromsome of D. melanogaster. I. Maternal effect mutations. Genetics 121: 101–117. Spradling AC, Rubin GM (1982): Transposition of cloned P elements into Drosophila germ line chromosomes. Science 218: 341–347. Steller H, Pirrotta V (1985): A transposable P vector that confers selectable G418 resistance to Drosophila larvae. EMBO J 4: 167–171. Struhl G, Struhl K, Macdonald PM (1989): The gradient morphogen bicoid is a concentration-dependent transcriptional activator. Cell 57: 1259–1273. Sullivan W, Minden J, Alberts B (1989): Dal, A maternal-effect mutation exhibiting abnormal cortical nuclear division. 30th Annual Drosophila Research Conference, 9.5: 9. Tautz D, Lehmann R, Schnurch H, Schuh R, Seifert E, Kienlin K, Jackle H (1987): Finger protein of novel structure encoded by hunchback, a second member of the gap class of Drosophila segmentation genes. Nature 327: 383–389. Tautz D, Pfeifle C (1989): A nonradioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback. Chromosoma 98: 81–85. Tolias PP, Kafatos FC (1990): Functional dissection of an early Drosophila chorion gene promoter: expression throughout the follicular epithelium is under spatially composite regulation. EMBO J 9: 1457–1464. Van Deusen EB (1977) Sex determination in germ line chimeras of D. melanogaster. J Embryol Exp Morphol 37: 173–185. Wieschaus E, Audit C, Masson M (1981): A clonal analysis of the roles of somatic cells and germ line during oogenesis in Drosophila. Dev Biol 88: 92–103. Wieschaus E, Marsh JL, Gehring W (1978): fs(1)K10, a germline-dependent female sterile mutation causing abnormal chorion morphology in D. melanogaster. Wilhelm Roux Arch 184: 75–82. Wilson C, Pearson RK, Bellen HJ, O'Kane CJ, Grossniklaus U, Gehring WJ (1989): P-element-mediated enhancer detection: An efficient method for isolating and characterizing developmentally regulated genes in Drosophila. Genes Dev 3: 1301–1313. Yedvobnick B, Krider HM, Levine BI (1980): Analysis of the autosomal mutation abo and its interaction with the ribosomal DNA of Drosophila melanogaster: The role of X-chromosome heterochromatin. Genetics 95: 661–672. Zhalokar M, Audit C, Erk I (1975): Developmental defects of female sterile mutants of D. melanogaster. Dev Biol 47: 419–432. Citing Literature Volume28, Issue3March 1991Pages 307-317 ReferencesRelatedInformation