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Single molecule mtDNA fiber FISH for analyzing numtogenesis.
Koo, Dal-Hoe; Singh, Bhupendra; Jiang, Jiming; Friebe, Bernd; Gill, Bikarm S; Chastain, Paul D; Manne, Upender; Tiwari, Hemant K; Singh, Keshav K.
Afiliación
  • Koo DH; Wheat Genetics Resources Center, Department of Plant Pathology, Throckmorton Plant Sciences Center, Kansas State University, Manhattan, KS 66506, United States.
  • Singh B; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, United States.
  • Jiang J; Department of Horticulture, University of Wisconsin-Madison, Madison, WI 53706, United States.
  • Friebe B; Wheat Genetics Resources Center, Department of Plant Pathology, Throckmorton Plant Sciences Center, Kansas State University, Manhattan, KS 66506, United States.
  • Gill BS; Wheat Genetics Resources Center, Department of Plant Pathology, Throckmorton Plant Sciences Center, Kansas State University, Manhattan, KS 66506, United States.
  • Chastain PD; College of Osteopathic Medicine, William Carey University, Hattiesburg, MS, United States.
  • Manne U; Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294, United States.
  • Tiwari HK; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL 35294, United States.
  • Singh KK; Departments of Genetics, Pathology, Environmental Health, Center for Free Radical Biology, Center for Aging, UAB Comprehensive Cancer Center, University of Alabama at Birmingham, AL 35294, United States; Birmingham Veterans Affairs Medical Center, Birmingham, AL 35294, United States. Electronic addr
Anal Biochem ; 552: 45-49, 2018 07 01.
Article en En | MEDLINE | ID: mdl-28322800
Somatic human cells contain thousands of copies of mitochondrial DNA (mtDNA). In eukaryotes, natural transfer of mtDNA into the nucleus generates nuclear mitochondrial DNA (NUMT) copies. We name this phenomenon as "numtogenesis". Numtogenesis is a well-established evolutionary process reported in various sequenced eukaryotic genomes. We have established a molecular tool to rapidly detect and analyze NUMT insertions in whole genomes. To date, NUMT analyses depend on deep genome sequencing combined with comprehensive computational analyses of the whole genome. This is time consuming, cumbersome and cost prohibitive. Further, most laboratories cannot accomplish such analyses due to limited skills. We report the development of single-molecule mtFIBER FISH (fluorescence in situ hybridization) to study numtogenesis. The development of mtFIBER FISH should aid in establishing a role for numtogenesis in cancers and other human diseases. This novel technique should help distinguish and monitor cancer stages and progression, aid in elucidation of basic mechanisms underlying tumorigenesis and facilitate analyses of processes related to early detection of cancer, screening and/or cancer risk assessment.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN Mitocondrial / Núcleo Celular / Hibridación Fluorescente in Situ Tipo de estudio: Risk_factors_studies / Screening_studies Límite: Humans Idioma: En Revista: Anal Biochem Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN Mitocondrial / Núcleo Celular / Hibridación Fluorescente in Situ Tipo de estudio: Risk_factors_studies / Screening_studies Límite: Humans Idioma: En Revista: Anal Biochem Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos