HETEROPLASMY IN HUMAN MITOCHONDRIAL DNA

ABSTRACT: <br /> <br /> <br /> Identification process through sequence determination of hypervariable segment I (HVSI) of mitochondrial DNA (mtDNA) could be done due to its high mutation rate. However, T16189C mutation, which leads to poli-cytosin stretch (poli-C), gives rise to t...

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主要作者: Dwiyanti (NIm 20504008), Faika
格式: Theses
語言:Indonesia
在線閱讀:https://digilib.itb.ac.id/gdl/view/7859
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機構: Institut Teknologi Bandung
語言: Indonesia
id id-itb.:7859
spelling id-itb.:78592017-09-27T15:39:40ZHETEROPLASMY IN HUMAN MITOCHONDRIAL DNA Dwiyanti (NIm 20504008), Faika Indonesia Theses INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/7859 ABSTRACT: <br /> <br /> <br /> Identification process through sequence determination of hypervariable segment I (HVSI) of mitochondrial DNA (mtDNA) could be done due to its high mutation rate. However, T16189C mutation, which leads to poli-cytosin stretch (poli-C), gives rise to the incompletion of sequence determination through direct sequencing shown by the unread sequences after the stretch. This problem has been solved using cloning method. Hypothetically, the failure of direct sequencing and the success of sequencing after cloning happened due to heteroplasmy phenomena. Several recombinant DNA clones of samples that have poli-C stretch are sequenced using Dideoxy Sanger method to test this hypothesis. Three out of four clones of GMR samples have 11C-long and the other has 12C-long poli-C stretch. Whereas for XXAM sample, two clones showed different length of poli-C stretch, i.e. 12C and 15C. This work has successfully shown the existence of heteroplasmy that can be proposed as the cause of incompletion in mtDNA HVSI sequence determination of sample containing poli-C stretch through direct sequencing. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description ABSTRACT: <br /> <br /> <br /> Identification process through sequence determination of hypervariable segment I (HVSI) of mitochondrial DNA (mtDNA) could be done due to its high mutation rate. However, T16189C mutation, which leads to poli-cytosin stretch (poli-C), gives rise to the incompletion of sequence determination through direct sequencing shown by the unread sequences after the stretch. This problem has been solved using cloning method. Hypothetically, the failure of direct sequencing and the success of sequencing after cloning happened due to heteroplasmy phenomena. Several recombinant DNA clones of samples that have poli-C stretch are sequenced using Dideoxy Sanger method to test this hypothesis. Three out of four clones of GMR samples have 11C-long and the other has 12C-long poli-C stretch. Whereas for XXAM sample, two clones showed different length of poli-C stretch, i.e. 12C and 15C. This work has successfully shown the existence of heteroplasmy that can be proposed as the cause of incompletion in mtDNA HVSI sequence determination of sample containing poli-C stretch through direct sequencing.
format Theses
author Dwiyanti (NIm 20504008), Faika
spellingShingle Dwiyanti (NIm 20504008), Faika
HETEROPLASMY IN HUMAN MITOCHONDRIAL DNA
author_facet Dwiyanti (NIm 20504008), Faika
author_sort Dwiyanti (NIm 20504008), Faika
title HETEROPLASMY IN HUMAN MITOCHONDRIAL DNA
title_short HETEROPLASMY IN HUMAN MITOCHONDRIAL DNA
title_full HETEROPLASMY IN HUMAN MITOCHONDRIAL DNA
title_fullStr HETEROPLASMY IN HUMAN MITOCHONDRIAL DNA
title_full_unstemmed HETEROPLASMY IN HUMAN MITOCHONDRIAL DNA
title_sort heteroplasmy in human mitochondrial dna
url https://digilib.itb.ac.id/gdl/view/7859
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