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Open AccessJournal ArticleDOI

The complete nucleotide sequence of the Xenopus laevis mitochondrial genome.

Bruce A. Roe, +3 more
- 15 Aug 1985 - 
- Vol. 260, Iss: 17, pp 9759-9774
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TLDR
Observations suggest that the mechanisms of replication, transcription, processing, and translation in mitochondria are highly conserved throughout higher vertebrates.
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This article is published in Journal of Biological Chemistry.The article was published on 1985-08-15 and is currently open access. It has received 702 citations till now. The article focuses on the topics: MT-RNR1 & Stop codon.

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Citations
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Journal ArticleDOI

Animal mitochondrial genomes

TL;DR: The comparison of animal mitochondrial gene arrangements has become a very powerful means for inferring ancient evolutionary relationships, since rearrangements appear to be unique, generally rare events that are unlikely to arise independently in separate evolutionary lineages.
Journal ArticleDOI

Ribosomal DNA: molecular evolution and phylogenetic inference.

TL;DR: An analysis of aligned sequences of the four nuclear and two mitochondrial rRNA genes identified regions of these genes that are likely to be useful to address phylogenetic problems over a wide range of levels of divergence.
Journal ArticleDOI

Evolution of animal mitochondrial dna: relevance for population biology and systematics

TL;DR: This work focuses on molecular aspects of animal mtDNA that are especially relevant to its use in evolutionary studies, and considers the form and frequency of three types of change in mtDNA: base substitution, length variation, and sequence rearrangement.
Book ChapterDOI

Animal mitochondrial DNA: structure and evolution.

TL;DR: The extent of size reduction within metazoan mitochondrial-transfer RNA (mt-tRNA) gene sets strongly correlates with the degree to which the more variable secondary structure element-forming regions of mt-rRNA genes are lost.
References
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Journal ArticleDOI

DNA sequencing with chain-terminating inhibitors

TL;DR: A new method for determining nucleotide sequences in DNA is described, which makes use of the 2',3'-dideoxy and arabinon nucleoside analogues of the normal deoxynucleoside triphosphates, which act as specific chain-terminating inhibitors of DNA polymerase.
Journal ArticleDOI

Sequence and organization of the human mitochondrial genome

TL;DR: The complete sequence of the 16,569-base pair human mitochondrial genome is presented and shows extreme economy in that the genes have none or only a few noncoding bases between them, and in many cases the termination codons are not coded in the DNA but are created post-transcriptionally by polyadenylation of the mRNAs.
Journal ArticleDOI

Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing

TL;DR: An approach to DNA sequencing using chain-terminating inhibitors (Sanger et al., 1977) combined with cloning of small fragments of DNA in a single-stranded DNA bacteriophage is described, determining the 2771-nucleotide sequence of the largest MboI restriction enzyme fragment from human mitochondrial DNA.
Journal ArticleDOI

A new pair of M13 vectors for selecting either DNA strand of double-digest restriction fragments.

TL;DR: Two new M13 vectors, M13MP8 and M13mp9, have been constructed that permit the cloning of the same restriction fragment in both possible orientations, allowing the use of only one of the two DNA strands as a template for M13 shotgun sequencing.
Journal ArticleDOI

Codon--anticodon pairing: the wobble hypothesis.

TL;DR: In this paper, it is suggested that while the standard base pairs may be used rather strictly in the first two positions of the triplet, there may be some wobble in the pairing of the third base.
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