scholarly journals Different nucleotide changes in the large rRNA gene of the mitochondrial DNA confer chloramphenicol resistance on two human cell lines

1981 ◽  
Vol 9 (21) ◽  
pp. 5785-5796 ◽  
Author(s):  
Hugues Blanc ◽  
Camellia W. Adams ◽  
Douglas C. Wallace
1997 ◽  
Vol 23 (4) ◽  
pp. 287-290 ◽  
Author(s):  
Isabelle Nelson ◽  
Michael G. Hanna ◽  
Nicholas W. Wood ◽  
A. E. Harding

A genetic analysis of the resistance phenotype of a recently described chloramphenicol-resistant variant derived from the human cell line, HeLa (MC63), has been undertaken. Whole cells or enucleated fragments, produced by treatment with cytochalasin B, were fused with chloram­phenicol-sensitive mouse, or human cells. Enucleated cells (cytoplasts) act as very efficient donors of the resistance phenotype in fusions with other human cell lines derived from HeLa. We conclude that chloram­phenicol resistance is determined cytoplasmically. Transfer of resistance to unrelated human cell lines occurred at much lower frequency and we were unable to demonstrate transfer to mouse cells. An examination of mitochondrial protein synthesis in the fusion products of cytoplasts and whole cells suggested that mixed populations of mitochondria from both parental cells were maintained under the conditions of selection.


2019 ◽  
Vol 20 (13) ◽  
pp. 3245 ◽  
Author(s):  
Matthew J. Young ◽  
Anitha D. Jayaprakash ◽  
Carolyn K. J. Young

The mitochondrial DNA (mtDNA) sequences of two commonly used human cell lines, HepaRG and SJCRH30, were determined. HepaRG originates from a liver tumor obtained from a patient with hepatocarcinoma and hepatitis C while SJCRH30 originates from a rhabdomyosarcoma patient tumor. In comparison to the revised Cambridge Reference Sequence, HepaRG and SJCRH30 mtDNA each contain 14 nucleotide variations. In addition to an insertion of a cytosine at position 315 (315insC), the mtDNA sequences from both cell types share six common polymorphisms. Heteroplasmic variants were identified in both cell types and included the identification of the 315insC mtDNA variant at 42 and 75% heteroplasmy in HepaRG and SJCRH30, respectively. Additionally, a novel heteroplasmic G13633A substitution in the HepaRG ND5 gene was detected at 33%. Previously reported cancer-associated mtDNA variants T195C and T16519C were identified in SJCRH30, both at homoplasmy (100%), while HepaRG mtDNA harbors a known prostate cancer-associated T6253C substitution at near homoplasmy, 95%. Based on our sequencing analysis, HepaRG mtDNA is predicted to lie within haplogroup branch H15a1 while SJCRH30 mtDNA is predicted to localize to H27c. The catalog of polymorphisms and heteroplasmy reported here should prove useful for future investigations of mtDNA maintenance in HepaRG and SJCRH30 cell lines.


Mitochondrion ◽  
2002 ◽  
Vol 1 (5) ◽  
pp. 425-435 ◽  
Author(s):  
Daciana H Margineantu ◽  
W Gregory Cox ◽  
Linda Sundell ◽  
Steven W Sherwood ◽  
Joseph M Beechem ◽  
...  

2015 ◽  
Vol 29 (S1) ◽  
Author(s):  
Shikha Gautam ◽  
Michelle Gulfo ◽  
Robert O'Donnell ◽  
Wendy Pogozelski

2004 ◽  
Vol 10 (5-6) ◽  
pp. 226-228
Author(s):  
L.M. Nosach ◽  
◽  
O.Yu. Povnitsa ◽  
V.L. Zhovnovata ◽  
◽  
...  

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