Ray, Malay Kumar (1985) Studies of cytoplasmically inherited genes for components of the mitochondrial ATP ase complex: analysis of the Oli-2 region of the mitrochondrial genome of 'Saccharomyces cerevisiae'. PhD thesis, University of Warwick.

Preview

PDF WRAP_Theses_Ray_1985.pdf - Unspecified Version - Requires a PDF viewer. Download (16Mb) | Preview

Request Changes to record.

Abstract

This thesis describes studies of the structure and organisation of the Oli-2 region of the mitochondrial genome from wild type, drug resistant (01i2 . Ossl ) and mit strains of the yeast Saccharomyces cercvisiac . In addition attempts have been made to identify the locus of cytoplasmic, nonmitochondrial markers (VENR , TET R, Rh8GR), to drugs which affect mitochondrial energy metabolism.

Firstly, a fine structure genetic map of the Oli-2 region of the mitochondrial genome has been generated by petite deletion mapping. Two mit mutations (pho8 and pho9) have been mapped upstream and one mit mutation (mit-175) has been mapped downstream of the 01i2 locus (Chapter-2). A problem was identified regarding the effect of a nuclear gene ( kar-1) on the copy number and transmission of petite (p ) mitochondrial genomes I Chapter-3). To circumvent this problem the relevent portions of the mitochondrial DNA l mt-DNA) from various mutants of the Oli-2 region have been cloned in a multicopy plasmid. pAT 153 of E. colI, for their amplification and propagation (Chapter-4).

The cloned DMAs have been sequenced using the single stranded phage, M 13 as a sequencing vector. A sequence of about 4000 bp. starting from the Carboxyl terminal end of cytochrome oxidase subunit-1 (Oxi-3) to 1500 bp downstream of 01i2 has been sequenced. Three main reading frames have been identified in this stretch of the DNA segment. The mutations (0/i'2 , Oa 1 ) leading to the resistivity towards the drugs oli- gomycin and ossamycin have been located in the reading frame for subunit-6. The mit mutation (pho9) has been found not to lie on the structural gene for subunit-8 which is located upstream of the gene for subunit-6. It is assumed that the mutation is possibly located in the intergenic regulatory region of the genes. A putative reading frame has been identified downstream of subunit-6 reading frame, which could be the possible site for the genetic locus, mit-175 (Chapter-5).

Models for the secondary and tertiary structures of subunit-6, subunit-8, and subunit-9 have been proposed on a theoretical basis using hydrophobicity plots and a modified Chou and Fasman method (Chou & Fasman, 1978). Suggestions as to the mechanism of inhibi­tion of oxidative phosphorylation by oligomycin and ossamycin have been made on the basis of these models. The present studies also indicate that subunit-8 has structural analogies to subunit-b of E. colt ATP synthetase (Chapter-6).
An attempt has also been made to identify a cytoplasmic candidate for nonmitochondrial, cytoplasmic genetic markers (P£,VR, TETR, Rh6GR) with special emphasis on studies of the 3 μ plasmid (Chapter-7). It has been demonstrated that the 2μ plasmid, or dsRNAs found in the cytoplasm are not the bearer of these genetic markers. In spite of the fact that the 3 μ DNA species under investigation has an insertion, no evidence has been obtained that the 3 μ plasmid contain the above markers. The existence of a high molec­ular weight plasmid in the cytoplasm of S. cercvisiae has also been demonstrated.

Item Type:	Thesis or Dissertation (PhD)
Subjects:	Q Science > QP Physiology
Library of Congress Subject Headings (LCSH):	Mitochondrial DNA, Saccharomyces -- Biotechnology, Molecular biology, Cytology -- Research, Mitochondrial pathology, Saccharomyces cerevisiae -- Genetics
Official Date:	February 1985
Dates:	Date Event February 1985 Submitted
Institution:	University of Warwick
Theses Department:	Department Chemistry
Thesis Type:	PhD
Publication Status:	Unpublished
Supervisor(s)/Advisor:	Griffiths, D. E.
Sponsors:	West Bengal (India)
Extent:	viii, 290 leaves : illustrations
Language:	eng

Request changes or add full text files to a record

Repository staff actions (login required)

View Item

Downloads