Stabilization of Z-RNA by chemical bromination and its recognition by anti-Z-DNA antibodies

Biochemistry ◽  
1987 ◽  
Vol 26 (16) ◽  
pp. 5191-5199 ◽  
Author(s):  
Charles C. Hardin ◽  
David A. Zarling ◽  
Joseph D. Puglisi ◽  
Mark O. Trulson ◽  
Peter W. Davis ◽  
...  
Keyword(s):  
1995 ◽  
Vol 48 (3) ◽  
pp. 215-219 ◽  
Author(s):  
Sadia Arjumand ◽  
Zarina Arif ◽  
Asif Ali ◽  
Rashid Ali
Keyword(s):  

1997 ◽  
Vol 45 (11) ◽  
pp. 1511-1521 ◽  
Author(s):  
Claude E. Gagna ◽  
W. Clark Lambert ◽  
Hon-Reen Kuo ◽  
Patricia N. Farnsworth

We examined histochemically and immunohistochemically the distribution of B- and Z-DNA in the epithelium and terminally differentiating dog lens fiber cells. On the basis of anti-DNA antibody reactivity, qualitative and quantitative data on B- and Z-DNA in cells were determined. Anti-B-DNA immunoreactivity gradually declined throughout nucleated fibers, with a precipitous decrease at ∼90 μm. Anti-Z-DNA antibody binding decreased with a sudden loss of immunoreactivity at ∼90 μm. The pattern of anti-B- and Z-DNA staining correlates with the loss of α-crystallin immunoreactivity, the major lens crystallin, and decreased eosin staining of proteins. Germinative zone cell nuclei showed the highest DNA probe binding values, followed by the superficial fibers, central zone, middle fibers, and deep fibers. The presence of single-stranded (ss)DNA in deeper fibers was detected by anti-ss-DNA antibodies. This is indicative of DNA degradation. These observations suggest that a dramatic reorganization of lens fiber cells' supramolecular order occurs at ∼90 μm, the phase transition zone. (J Histochem Cytochem 45:1511–1521, 1997)


1987 ◽  
Vol 75 (2) ◽  
pp. 114-119 ◽  
Author(s):  
E. Viegas-Pequignot ◽  
B. Malfoy ◽  
L. Sabatier ◽  
B. Dutrillaux

1985 ◽  
Vol 5 (11) ◽  
pp. 3270-3273 ◽  
Author(s):  
L Staiano-Coico ◽  
B D Stollar ◽  
Z Darzynkiewicz ◽  
R Dutkowski ◽  
M E Weksler

Although regions of DNA reacting with anti-Z-DNA antibodies have been identified in the polytene chromosomes of Drosophila spp. and the metaphase chromosomes from a number of different mammalian species, the biological role of this DNA is unknown. Flow cytometry was used in the present studies to quantitate the binding of anti-Z-DNA antibodies in quiescent and activated human peripheral blood lymphocytes; the antibody binding was then correlated with cell cycle phase. The data show that quiescent (G0 or G1Q) lymphocytes are heterogeneous with respect to their reaction with anti-Z-DNA antibodies. The transition from quiescence (G1Q) into the cell cycle (G1), which involves decondensation of chromatin, did not result in any significant change in binding of these antibodies. In contrast, progression of cells from G1 through S and G2 is correlated with a 27% decrease in anti-Z-DNA antibody reactivity relative to total DNA content. No significant change was observed during the transition from G2 to mitosis (M).


1993 ◽  
Vol 294 (2) ◽  
pp. 419-425 ◽  
Author(s):  
T J Thomas ◽  
J R Seibold ◽  
L E Adams ◽  
E V Hess

We studied the effect of hydralazine, an antihypertensive drug with lupus-inducing side effects, on the conformation of poly(dG-m5dC).poly(dG-m5dC) and a plasmid with a 23 bp insert of (dG-dC)n.(dG-dC)n sequences. Using an e.l.i.s.a. with a monoclonal anti-(Z-DNA) antibody Z22, we found that hydralazine provoked the Z-DNA conformation in poly(dG-m5dC).poly(dG-m5dC) at 250-500 microM concentration. The supercoiled form of hydralazine-treated plasmid bound to Z22 in a gel-retardation assay. To examine further whether Z-DNA could act as an inciting agent in anti-nuclear antibody production in patients, we analysed 65 sera from 25 hypertensive patients taking hydralazine and found anti-(Z-DNA) antibodies in 82% of these sera. Sera from age-matched normal controls showed no binding to Z-DNA. Data on sera drawn sequentially from four hypertensive patients showed that antibodies were present after the drug treatment. These data demonstrate the presence of a high incidence of anti-(Z-DNA) antibodies in patients treated with hydralazine and suggest that a possible mechanism for the production of autoantibodies in drug-related lupus might involve the induction and stabilization of Z-DNA by drugs.


1994 ◽  
Vol 298 (2) ◽  
pp. 485-491 ◽  
Author(s):  
T J Thomas ◽  
T Thomas

Blocks of potential Z-DNA-forming (dA-dC)n.(dG-dT)n sequences are ubiquitous in eukaryotic genomes. We examined whether naturally occurring polyamines, putrescine, spermidine and spermine, could provoke the Z-DNA conformation in plasmids pDHf2 and pDHf14 with 23 and 60 bp inserts respectively of (dA-dC)n.(dG-dT)n sequences using an e.l.i.s.a. Spermidine and spermine could provoke Z-DNA conformation in these plasmids, but putrescine was ineffective. For pDHf2 and pDHf14, the concentration of spermidine at the midpoint of B-DNA to Z-DNA transition was 25 microM, whereas that of spermine was 16 microM. Polyamine structural specificity was evident in the ability of spermidine homologues to induce Z-DNA. Inorganic cations, Co(NH3)6(3+) and Ru(NH3)6(3+), were ineffective. Our experiments also showed increased binding of anti-DNA autoantibodies from lupus patients as well as autoimmune MRL-lpr/lpr mice to pDHf2 and pDHf14 in the presence of polyamines. These data demonstrate that small blocks of (dA-dC)n.(dG-dT)n sequences could assume the Z-DNA conformation in the presence of natural polyamines. Increased concentrations of polyamines in the sera of lupus patients might facilitate immune complex-formation involving circulating DNA and anti-Z-DNA antibodies.


1987 ◽  
Vol 15 (4) ◽  
pp. 1661-1677 ◽  
Author(s):  
Alfred Nordheim ◽  
Rafael E. Herrera ◽  
Alexander Rich
Keyword(s):  
Z Dna ◽  

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