scholarly journals Meiotic segregation analysis of restriction site polymorphisms allows rapid genetic mapping

1986 ◽  
Vol 5 (6) ◽  
pp. 1125-1127 ◽  
Author(s):  
Ute Raeder ◽  
Paul Broda
1993 ◽  
Vol 111 (2-3) ◽  
pp. 239-243 ◽  
Author(s):  
David Ralph ◽  
Daniele Postic ◽  
Guy Baranton ◽  
Charles Pretzman ◽  
Michael McClelland

1982 ◽  
Vol 2 (1) ◽  
pp. 30-41
Author(s):  
N A Oliver ◽  
D C Wallace

Two mitochondrially synthesized marker polypeptides, MV-1 and MV-2, were found in human HeLa and HT1080 cells. These were assigned to the mitochondrial DNA in HeLa-HT1080 cybrids and hybrids by demonstrating their linkage to cytoplasmic genetic markers. These markers include mitochondrial DNA restriction site polymorphisms and resistance to chloramphenicol, an inhibitor of mitochondrial protein synthesis. In the absence of chloramphenicol, the expression of MV-1 and MV-2 in cybrids and hybrids was found to be directly proportional to the ratio of the parental mitochondrial DNAs. In the presence of chloramphenicol, the marker polypeptide linked to the chloramphenicol-sensitive mitochondrial DNA continued to be expressed. This demonstrated that resistant and sensitive mitochondrial DNAs can cooperate within a cell for gene expression and that the CAP-resistant allele was dominant or codominant to sensitive. Such cooperation suggests that mitochondrial DNAs can be exchanged between mitochondria.


2014 ◽  
Vol 59 (12) ◽  
pp. 667-674 ◽  
Author(s):  
Alina Teresa Midro ◽  
Barbara Panasiuk ◽  
Beata Stasiewicz-Jarocka ◽  
Marta Olszewska ◽  
Ewa Wiland ◽  
...  

2011 ◽  
Vol 155 (5) ◽  
pp. 1157-1161 ◽  
Author(s):  
Miluse Vozdova ◽  
Vera Horinova ◽  
Vendula Wernerova ◽  
Romana Skalikova ◽  
Roman Rybar ◽  
...  

1984 ◽  
Vol 4 (5) ◽  
pp. 978-981 ◽  
Author(s):  
C Blatt ◽  
M E Harper ◽  
G Franchini ◽  
M N Nesbitt ◽  
M I Simon

The murine homologs of two viral oncogenes associated with tyrosine-specific kinase activity have been assigned to different loci in the mouse genome. The segregation of restriction site polymorphisms, as detected by probes that are specific for endogenous c-fes and c-src sequences, was followed in the DNA of recombinant inbred strains. The c-fes gene was mapped to the proximal portion of chromosome 7, very close to the Gpi-1 locus, whereas c-src was linked to the Psp locus on the distal half of chromosome 2.


2000 ◽  
Vol 66 (1) ◽  
pp. 167-175 ◽  
Author(s):  
Anne Girardet ◽  
Mary Sara McPeek ◽  
Esther P. Leeflang ◽  
Francis Munier ◽  
Norman Arnheim ◽  
...  

Genetics ◽  
1994 ◽  
Vol 136 (3) ◽  
pp. 1121-1141 ◽  
Author(s):  
O P Das ◽  
J Messing

Abstract Two instances of genetic transmission of spontaneous epimutation of the maize P-rr gene were identified. Transmission gave rise to two similar, moderately stable alleles, designated P-pr-1 and P-pr-2, that exhibited Mendelian behavior. Both isolates of P-pr conditioned a variable and variegated phenotype, unlike the uniform pigmentation conditioned by P-rr. Extensive genomic analysis failed to reveal insertions, deletions or restriction site polymorphisms between the new allele and its progenitor. However, methylation of the P gene was increased in P-pr relative to P-rr, and was greatly reduced (though not lost) in a revertant to uniform pigmentation. Variability in pigmentation conditioned by P-pr correlated with variability in transcript levels of the P gene, and both correlated inversely with variability in its methylation. Part of the variability in methylation could be accounted for by a developmental decrease in methylation in all tissues of plants carrying P-pr. We hypothesize that the variegated phenotype results from a general epigenetic pathway which causes a progressive decrease in methylation and increase in expression potential of the P gene as a function of cell divisions in each meristem of the plant. This renders all tissues chimeric for a functional gene; chimerism is visualized as variegation only in pericarp due to the tissue specificity of P gene expression. Therefore, this allele that originates from epimutation may exemplify an epigenetic mechanism for variegation in maize.


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