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Nucleic Acids Res ; 28(22): 4444-51, 2000 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-11071931

RESUMO

The 3'-termini of maize mitochondrial RNAs were characterized by ligation of an anchor oligonucleotide, reverse transcription and amplification. DNA sequence analysis of cDNA clones for tRNA(Ser) and 18S rRNA confirmed the expected 3'-terminal nucleotides and demonstrated the accuracy and fidelity of the protocol. Analysis of cDNAs for rps12, cox2 and atp9 indicated that non-genomically encoded nucleotides were present at the 3'-terminus. rps12 cDNAs exhibited the highest degree of modification, with 94% of 35 cDNA clones analyzed containing one to four non-genomically encoded C or A residues; 83% of these cDNAs terminated with the trinucleotide CCA. DNA sequence and transcript mapping analyses demonstrated that four positions exhibited modified 3'-termini within a small region of the 3' flank of rps12 transcripts. These transcript termini represented low abundance, truncated forms of rps12 mRNAs which may be intermediates in degradation. cox2 mRNAs are also modified at a truncated position. Sixty percent of the cox2 cDNAs were modified with 1-5 nt that most frequently included A and C residues, but also included a few G and T residues. Non-genomically encoded nucleotides were detected in 27% of the atp9 cDNAs as a single C or A residue.


Assuntos
Regiões 3' não Traduzidas/genética , Mitocôndrias/genética , ATPases Mitocondriais Próton-Translocadoras , RNA de Plantas/genética , Zea mays/genética , Proteínas de Arabidopsis , Sequência de Bases , DNA Complementar/química , DNA Complementar/genética , Complexo IV da Cadeia de Transporte de Elétrons/genética , Dados de Sequência Molecular , Proteínas de Plantas/genética , Proteolipídeos/genética , ATPases Translocadoras de Prótons/genética , Processamento Pós-Transcricional do RNA , RNA Mensageiro/genética , RNA Ribossômico 18S/genética , RNA de Transferência de Serina/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Análise de Sequência de DNA
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