scholarly journals Transfer RNA genes in the cap-oxil region of yeast mitochondrial DNA

1980 ◽  
Vol 8 (21) ◽  
pp. 5017-5030 ◽  
Author(s):  
Roberta E. Berlani ◽  
Susan G. Bonitz ◽  
Gloria Coruzzi ◽  
Marina Nobrega ◽  
Alexander Tzagoloff
Gene ◽  
1981 ◽  
Vol 16 (1-3) ◽  
pp. 297-307 ◽  
Author(s):  
Kobayashi Midori ◽  
Seki Tetsunori ◽  
Yaginuma Katsuyuki ◽  
Koike Katsuro

1974 ◽  
Vol 88 (4) ◽  
pp. 735-747 ◽  
Author(s):  
James W. Casey ◽  
Huey-Juang Hsu ◽  
Godfrey S. Getz ◽  
Murray Rabinowitz ◽  
Hiroshi Fukuhara

Zootaxa ◽  
2019 ◽  
Vol 4652 (1) ◽  
pp. 126-134 ◽  
Author(s):  
JUN LI ◽  
KUNJIE HU ◽  
YAQI ZHAO ◽  
RUIRUI LIN ◽  
YAOYAO ZHANG ◽  
...  

In this study, the complete mitochondrial DNA sequence of Parum colligata (Lepidoptera: Sphingidae: Smerinthinae) was sequenced firstly. The mitogenome is 15,288 bp in size, containing 13 protein-coding genes (PCGs), 22 transfer RNA genes (tRNAs), two ribosomal RNA genes (rRNAs), and an A+T-rich region. In the mitogenome, Ile, Leu2, and Phe are the most frequently used codon families, while codons GCG, TGC, GGC, CTG, AGG, and ACG are absent. The A+T-rich region is 358 bp in length including a motif ‘ATAGA’, an 18 bp poly-T stretch, three copies of a 12 bp ‘TATATATATATA’, and a short poly-A element. The nucleotides sequence of A+T-rich region is closer to Sphinginae than Macroglossinae. Phylogenetic analyses, based on the PCGs by using Maximum Likelihood (ML) and Bayesian Inference (BI) methods, generated consistent results that Smerinthinae was clustered together with Sphinginae to be the sister groups rather than Macroglossinae. 


1974 ◽  
Vol 88 (4) ◽  
pp. 717-733 ◽  
Author(s):  
James W. Casey ◽  
Huey-Juang Hsu ◽  
Murray Rabinowitz ◽  
Godfrey S. Getz ◽  
Hiroshi Fukuhara

1980 ◽  
Vol 255 (24) ◽  
pp. 11922-11926 ◽  
Author(s):  
S.G. Bonitz ◽  
G. Coruzzi ◽  
B.E. Thalenfeld ◽  
A. Tzagoloff ◽  
G. Macino

1988 ◽  
Vol 8 (6) ◽  
pp. 2361-2366 ◽  
Author(s):  
K A Jarrell ◽  
R C Dietrich ◽  
P S Perlman

A self-splicing group II intron of yeast mitochondrial DNA (aI5g) was divided within intron domain 4 to yield two RNAs that trans-spliced in vitro with associated trans-branching of excised intron fragments. Reformation of the domain 4 secondary structure was not necessary for the trans reaction, since domain 4 sequences were shown to be dispensable. Instead, the trans reaction depended on a previously unpredicted interaction between intron domain 5, the most highly conserved region of group II introns, and another region of the RNA. Domain 5 was shown to be essential for cleavage at the 5' splice site. It stimulated that cleavage when supplied as a trans-acting RNA containing only 42 nucleotides of intron sequence. The relevance of our findings to in vivo trans-splicing mechanisms is discussed.


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