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The Arabidopsis nuclear DAL gene encodes a chloroplast protein which is required for the maturation of the plastid ribosomal RNAs and is essential for chloroplast differentiation
Authors:Bisanz  Cordelia  Bégot  Laurent  Carol  Pierre  Perez  Pascual  Bligny  Muriel  Pesey  Hélène  Gallois   Jean-Luc  Lerbs-Mache  Silva  Mache  Régis
Affiliation:(1) Laboratoire Plastes et Differenciation cellulaire, Université Joseph Fourier et Centre National de la Recherche Scientifique (CNRS), UMR 5575, BP53, 38041 Grenoble cedex 9, France;(2) Present address: Lab. PEGM, CERMO, BP53, 38041 Grenoble cedex 9, France;(3) Present address: I.M.A.S.S.A, BP 73, 91223 Brétigny sur Orge, France;(4) Present address: Cell and Dev. Biol., John Innes Centre, Norwich, NR4 7UH, United Kingdom
Abstract:Altered pigmentation is an easily scored and sensitive monitor of plastid function. We analyzed in detail a yellow colored transposon-tagged mutant (dal1-2) that is allelic to the dal mutant previously identified (Babiychuk et al., 1997). Mesophyll cells of mutant plants possess abnormal nucleoids and more but smaller plastids than wild type cells. Plastid development in dal1-2 is not altered in the dark but is arrested at the early steps of thylakoid assembly. The amino acid sequence of the protein deduced from our cDNA clone is 21 amino acids longer than the previously published DAL sequence (Babiychuk et al., 1997) and allowed us to show that DAL codes for a chloroplast protein. The dal1-2 mutation has a global negative effect on plastid RNA accumulation and on expression of nuclear encoded photosynthetic genes. We show that the plastid RNA polymerases, the nuclear-encoded NEP and the plastid-encoded PEP, are functional in the mutant. Precursor 16S and 23S rRNA species specifically accumulate at a high level in the mutant but the 5prime-end and the long 3prime-end trailer are not modified. We suggest that the dal mutation is involved in plastid rRNA processing and consequently in translation and early chloroplast differentiation.
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