𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A mutation causing variegation and abnormal development in tobacco is associated with an altered mitochondrial DNA

✍ Scribed by H.T. Bonnett; I. Djurberg; M. Fajardo; K. Glimelius


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
981 KB
Volume
3
Category
Article
ISSN
0960-7412

No coin nor oath required. For personal study only.

✦ Synopsis


A variegated mutation appeared in the leaves of a tobacco cybrid plant resulting from fusion of protoplasts from tobacco with Petunia. The mutation was inherited maternally. The light green coloration of leaf sectors resulted from a substitution of spongy parenchyma for palisade parenchyma. No defects were detected in the chloroplasts of the plants, which were derived from Petunia. The mitochondria, as judged by the electrophoretic pattern of their DNA after digestion with restriction endonucleases, were very similar to mitochondria of tobacco, although with some unique cybrid‐specific fragments. A second round of fusions was performed to confirm that mitochondria, rather than chloroplasts, were associated with the variegated phenotype. In these fusions, the Petunia chloroplasts of the variegated plants were replaced by tobacco chloroplasts. The mitochondria, according to the DNA restriction pattern, retained all or some of the unique cybrid‐specific fragments found in the original variegated tobacco cybrid. Since the variegated phenotype remained after the chloroplast exchange, the chloroplast DNA cannot be the site of the mutation which is responsible for the mutant phenotype. This result eliminates the chloroplast and confirms that the mitochondrial genome is associated with the mutant phenotype.


📜 SIMILAR VOLUMES


A novel recurrent mitochondrial DNA muta
✍ Emmanuelle Sarzi; Michael D. Brown; Sophie Lebon; Dominique Chretien; Arnold Mun 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 156 KB 👁 2 views

## Abstract Defects in NADH:ubiquinone oxidoreductase (complex I), the largest complex of the mitochondrial respiratory chain, account for most cases of respiratory chain deficiency in human. Complex I contains at least 45 subunits, 7 of which are encoded by mitochondrial DNA (mtDNA). Here we repor

m.6267G>A: a recurrent mutation in the h
✍ M. Esther Gallardo; Raquel Moreno-Loshuertos; Celia López; Mercedes Casqueiro; J 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 259 KB

Complete sequencing of the mitochondrial genome of 13 cell lines derived from a variety of human cancers revealed nine novel mitochondrial DNA (mtDNA) variations. One of them, m.6267G>A, is a recurrent mutation that introduces the Ala122Thr substitution in the mitochondrially encoded cytochrome c ox