نتایج جستجو برای: heteroplasmy

تعداد نتایج: 700  

Journal: :Journal of forensic sciences 2004
Kazumasa Sekiguchi Hajime Sato Kentaro Kasai

A denaturing gradient gel electrophoresis (DGGE) assay was used to detect mitochondrial DNA (mtDNA) sequence heteroplasmy in 160 hairs from each of three individuals. The HV1 and HV2 heteroplasmic positions were then identified by sequencing. In several hairs, the heteroplasmic position was not evident by sequencing and dHPLC separation of the homoduplex/heteroduplex species was carried out wit...

2016
Ruoyu Zhang Kiichi Nakahira Xiaoxian Guo Augustine M.K. Choi Zhenglong Gu

Cell free DNA (cfDNA) has received increasing attention and has been studied in a broad range of clinical conditions. However, few studies have focused on mitochondrial DNA (mtDNA) in the cell free form. We optimized DNA isolation and sequencing library preparation protocols to better retain short DNA fragments from plasma, and applied these optimized methods to plasma samples from patients wit...

Journal: :The Journal of heredity 2010
Brenna A McLeod Bradley N White

Mitochondrial heteroplasmy has been identified in a variety of species and can result from either paternal leakage, whereby sperm mitochondria enter the ova during fertilization, or more commonly by the "survival" and proliferation of mutant variants within an organism. From an evolutionary perspective, this process represents the generation of new mitochondrial diversity within a species. Alth...

Journal: :Cell 2015
Pradeep Reddy Alejandro Ocampo Keiichiro Suzuki Jinping Luo Sandra R. Bacman Sion L. Williams Atsushi Sugawara Daiji Okamura Yuji Tsunekawa Jun Wu David Lam Xiong Xiong Nuria Montserrat Concepcion Rodriguez Esteban Guang-Hui Liu Ignacio Sancho-Martinez Dolors Manau Salva Civico Francesc Cardellach Maria del Mar O’Callaghan Jaime Campistol Huimin Zhao Josep M. Campistol Carlos T. Moraes Juan Carlos Izpisua Belmonte

Mitochondrial diseases include a group of maternally inherited genetic disorders caused by mutations in mtDNA. In most of these patients, mutated mtDNA coexists with wild-type mtDNA, a situation known as mtDNA heteroplasmy. Here, we report on a strategy toward preventing germline transmission of mitochondrial diseases by inducing mtDNA heteroplasmy shift through the selective elimination of mut...

2013
Elizabeth E. Boyle Ron J. Etter

Most metazoan species have strict maternal inheritance of the mitochondrial genome. In bivalves, a unique inheritance pattern called doubly uniparental inheritance (DUI) occurs in at least seven bivalve families. In this system of mitochondrial inheritance, males inherit and carry mtDNA from both parents, while females only carry mtDNA from the mother. Here, we present evidence of mitochondrial...

2014
Claudia Calabrese Domenico Simone Maria Angela Diroma Mariangela Santorsola Cristiano Guttà Giuseppe Gasparre Ernesto Picardi Graziano Pesole Marcella Attimonelli

MOTIVATION The increasing availability of mitochondria-targeted and off-target sequencing data in whole-exome and whole-genome sequencing studies (WXS and WGS) has risen the demand of effective pipelines to accurately measure heteroplasmy and to easily recognize the most functionally important mitochondrial variants among a huge number of candidates. To this purpose, we developed MToolBox, a hi...

2012
Maria Ximena Sosa I. K. Ashok Sivakumar Samantha Maragh Vamsi Veeramachaneni Ramesh Hariharan Minothi Parulekar Karin M. Fredrikson Timothy T. Harkins Jeffrey Lin Andrew B. Feldman Pramila Tata Georg B. Ehret Aravinda Chakravarti

We describe methods for rapid sequencing of the entire human mitochondrial genome (mtgenome), which involve long-range PCR for specific amplification of the mtgenome, pyrosequencing, quantitative mapping of sequence reads to identify sequence variants and heteroplasmy, as well as de novo sequence assembly. These methods have been used to study 40 publicly available HapMap samples of European (C...

Journal: :Biology letters 2007
Beata Ujvari Mark Dowton Thomas Madsen

Mitochondrial DNA (mtDNA) is the traditional workhorse for reconstructing evolutionary events. The frequent use of mtDNA in such analyses derives from the apparent simplicity of its inheritance: maternal and lacking bi-parental recombination. However, in hybrid zones, the reproductive barriers are often not completely developed, resulting in the breakdown of male mitochondrial elimination mecha...

2008
Lynsey M Cree David C Samuels Susana Chuva de Sousa Lopes Harsha Karur Rajasimha Passorn Wonnapinij Jeffrey R Mann Hans-Henrik M Dahl Patrick F Chinnery

Mammalian mitochondrial DNA (mtDNA) is inherited principally down the maternal line, but the mechanisms involved are not fully understood. Females harboring a mixture of mutant and wild-type mtDNA (heteroplasmy) transmit a varying proportion of mutant mtDNA to their offspring. In humans with mtDNA disorders, the proportion of mutated mtDNA inherited from the mother correlates with disease sever...

2013
Erin A. Tripp Siti Fatimah Iain Darbyshire Lucinda A. McDade

Gene flow between closely related species is a frequent phenomenon that is known to play important roles in organismal evolution. Less clear, however, is the importance of hybridization between distant relatives. We present molecular and morphological evidence that support origin of the plant genus Physacanthus via "wide hybridization" between members of two distantly related lineages in the la...

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