Literature DB >> 6154711

Cell differentiation and flagellar elongation in Naegleria gruberi. Dependence on transcription and translation.

C Fulton, C Walsh.   

Abstract

This paper presents evidence that the phenotypic transformation of Naegleria gruberi from amebae to flagellates that occurs when cells are placed in a nutrient-free aqueous environment is dependent on transcription and translation. RNA and protein are synthesized during the hour-long differentiation. Actinomycin D and daunomycin selectively inhibit RNA synthesis, and cycloheximide selectively inhibits protein synthesis, throughout the time required for differentiation. These inhibitors prevent differentiation if added soon after the cells are transferred to nonnutrient buffer but cease to block specific differentiation events at subsequent, reproducible times, the transition points. After each transition point, morphogenesis can occur in the presence of the inhibitor and in the virtual absence of transcription or translation. A map of the transition points indicates that RNA synthesis is required until halfway through the temporal process from initiation to flagellum assembly, and that protein synthesis is required until three-fourths of the way through. Even when flagellum outgrowth can occur in the presence of cycloheximide, the length of the flagella formed is determined by the extent of synthesis of an unknown "limiting precursor." The transition points for formation of flagella and for formation of the streamlined flagellate body shape are temporally separate. These results indicate that differentiation in Naegleria involves a redirection of cell metabolism to produce new RNA and protein molecules that are essential for morphogenesis.

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Year:  1980        PMID: 6154711      PMCID: PMC2110630          DOI: 10.1083/jcb.85.2.346

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  39 in total

1.  Induction of microtubule protein synthesis in Chlamydomonas reinhardi during flagellar regeneration.

Authors:  D P Weeks; P S Collis
Journal:  Cell       Date:  1976-09       Impact factor: 41.582

2.  Programmed synthesis of tubulin for the flagella that develop during cell differentiation in Naegleria gruberi.

Authors:  J D Kowit; C Fulton
Journal:  Proc Natl Acad Sci U S A       Date:  1974-07       Impact factor: 11.205

Review 3.  Control of enzyme levels in animal tissues.

Authors:  R T Schimke; D Doyle
Journal:  Annu Rev Biochem       Date:  1970       Impact factor: 23.643

4.  Regulation of protein synthesis in mammalian cells. V. Further studies on the effect of actinomycin D on translation control in HeLa cells.

Authors:  E S Goldstein; S Penman
Journal:  J Mol Biol       Date:  1973-10-25       Impact factor: 5.469

5.  Sporulation in Physarum polycephalum: a model system for studies on differentiation.

Authors:  H W Sauer; K L Babcock; H P Rusch
Journal:  Exp Cell Res       Date:  1969-10       Impact factor: 3.905

6.  Intracellular regulation of cell shape and motility in Naegleria. First insights and a working hypothesis.

Authors:  C Fulton
Journal:  J Supramol Struct       Date:  1977

7.  Cycloheximide is not a specific inhibitor of protein synthesis in vivo.

Authors:  D McMahon
Journal:  Plant Physiol       Date:  1975-05       Impact factor: 8.340

8.  Programmed appearance of translatable flagellar tubulin mRNA during cell differentiation in Naegleria.

Authors:  E Y Lai; C Walsh; D Wardell; C Fulton
Journal:  Cell       Date:  1979-08       Impact factor: 41.582

9.  Flagellar regeneration in Chlamydomonas reinhardtii: evidence that cycloheximide pulses induce a delay in morphogenesis.

Authors:  K W Farrell
Journal:  J Cell Sci       Date:  1976-05       Impact factor: 5.285

10.  Basal bodies, but not centrioles, in Naegleria.

Authors:  C Fulton; A D Dingle
Journal:  J Cell Biol       Date:  1971-12       Impact factor: 10.539

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  13 in total

Review 1.  To shape a cell: an inquiry into the causes of morphogenesis of microorganisms.

Authors:  F M Harold
Journal:  Microbiol Rev       Date:  1990-12

2.  rRNA genes of Naegleria gruberi are carried exclusively on a 14-kilobase-pair plasmid.

Authors:  C G Clark; G A Cross
Journal:  Mol Cell Biol       Date:  1987-09       Impact factor: 4.272

3.  Transcriptional regulation of coordinate changes in flagellar mRNAs during differentiation of Naegleria gruberi amebae into flagellates.

Authors:  J H Lee; C J Walsh
Journal:  Mol Cell Biol       Date:  1988-06       Impact factor: 4.272

4.  Biological factors affecting enflagellation of Naegleria fowleri.

Authors:  T W Woodworth; D T John; S G Bradley
Journal:  J Bacteriol       Date:  1982-11       Impact factor: 3.490

5.  Nucleolus-like morphology produced during the in vitro reassociation of nucleolar components.

Authors:  G M Trimbur; C J Walsh
Journal:  J Cell Biol       Date:  1993-08       Impact factor: 10.539

6.  mRNAs for microtubule proteins are specifically colocalized during the sequential formation of basal body, flagella, and cytoskeletal microtubules in the differentiation of Naegleria gruberi.

Authors:  J W Han; J H Park; M Kim; J Lee
Journal:  J Cell Biol       Date:  1997-05-19       Impact factor: 10.539

7.  Synthesis and assembly of the cytoskeleton of Naegleria gruberi flagellates.

Authors:  C Walsh
Journal:  J Cell Biol       Date:  1984-02       Impact factor: 10.539

8.  mRNAs for alpha- and beta-tubulin and flagellar calmodulin are among those coordinately regulated when Naegleria gruberi amebae differentiate into flagellates.

Authors:  D K Shea; C J Walsh
Journal:  J Cell Biol       Date:  1987-09       Impact factor: 10.539

9.  New poly(A)+RNAs appear coordinately during the differentiation of Naegleria gruberi amebae into flagellates.

Authors:  J Mar; J H Lee; D Shea; C J Walsh
Journal:  J Cell Biol       Date:  1986-02       Impact factor: 10.539

10.  Two calmodulins in Naegleria flagellates: characterization, intracellular segregation, and programmed regulation of mRNA abundance during differentiation.

Authors:  C Fulton; K L Cheng; E Y Lai
Journal:  J Cell Biol       Date:  1986-05       Impact factor: 10.539

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