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  • 1
    ISSN: 1432-0983
    Keywords: Key words  Sorghum ; Mitochondrial DNA ; orf25 ; Cytoplasmic male sterility
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract   We describe fundamental characteristics of sorghum mitochondrial orf25, urf209, and a related chimeric configuration, orf265/130, which is restricted to the IS1112C source of cytoplasmic male sterility in sorghum. Transcripts of urf209 are edited at ten nucleotides, resulting in nine amino-acid changes predicted from genomic sequences. The cDNA-predicted polypeptide product is 23.6 kDa, while Western blot analyses identify a product of 20 kDa. Transcription of urf209 is characterized by one or two transcripts, dependent on nuclear background, but this difference is not related to male fertility status. The orf265/130 chimeric region includes 288 bp 95% identical to sequences 5′ to maize T-cytoplasm T-urf13 and atp6, which includes a common transcription initiation site, and terminates with a recombinational event involving urf209. The urf209 similarity extends 189 bp, followed by sequences duplicated 5′ to sorghum atp6-2. Sequences immediately 3′ to the atp6-2 similarity include a second in-frame start codon, defining orf130. Structural features 5′ to orf130 are shared with motifs found 5′ to several translated mitochondrial open reading frames. The orf265/orf130 configuration is uniquely transcribed, and transcripts of orf130 exhibit one silent RNA editing event. Transcription in somatic cells is not altered by male fertility status.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0983
    Keywords: Sorghum ; Mitochondrial DNA ; orf25 ; Cytoplasmic male sterility
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We describe fundamental characteristics of sorghum mitochondrial orf25,urf209, and a related chimeric configuration,orf265/130, which is restricted to the IS1112C source of cytoplasmic male sterility in sorghum. Transcripts ofurf209 are edited at ten nucleotides, resulting in nine amino-acid changes predicted from genomic sequences. The eDNA-predicted polypeptide product is 23.6 kDa, while Western blot analyses identify a product of 20 kDa. Transcription ofurf209 is characterized by one or two transcripts, dependent on nuclear background, but this difference is not related to male fertility status. Theorf265/130 chimeric region includes 288 by 95% identical to sequences 5′ to maize T-cytoplasmT-urf13 andatp6, which includes a common transcription initiation site, and terminates with a recombinational event involvingurf209. Theurf209 similarity extends 189 bp, followed by sequences duplicated 5′ to sorghumatp6-2. Sequences immediately 3′ to theatp6-2 similarity include a second inframe start codon, definingorf130. Structural features 5′ toorf130 are shared with motifs found 5′ to several translated mitochondrial open reading frames. Theorf265/orf130 configuration is uniquely transcribed, and transcripts oforf130 exhibit one silent RNA editing event. Transcription in somatic cells is not altered by male fertility status.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    ISSN: 1432-0983
    Keywords: Key words Cytoplasmic male sterility (CMS) ; Sorghum bicolor ; Tissue-specific mitochondrial ; RNA editing ; Pollen development
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract RNA editing and cytoplasmic male sterility are two important phenomena associated with higher plant mitochondria. We recently have shown a potential function of RNA editing in CMS development. The frequency of atp6 RNA editing was specifically reduced in anthers of male-sterile Sorghum bicolor, which increased in frequency in partially restored progeny. Here we present data that show that the loss of RNA editing capability also occurs in a second nuclear background that allows the expression of male sterility. Loss of RNA editing thus appears to be associated with unique combinations of male-sterile cytoplasm and non-restoring nuclear backgrounds. In addition, the reduction of RNA editing affects both gametophytic and sporophytic anther cell-types but not other floral tissues. An analysis of F2 plants exhibiting different levels of fertility indicates a co-segregation of fertility restoration and atp6 RNA editing. The atp6 transcript abundance is similar in seedlings and anthers of male-sterile, partially restored, and male-fertile lines and thus is not associated with loss of atp6 RNA editing in anthers. A model for RNA editing and male sterility based on the data available is presented. Functional correlations with other CMS systems are also discussed.
    Type of Medium: Electronic Resource
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