<p>The <i>mgrA</i> gene has two promoters, depicted in (C). Lines labeled P2 and P1 show the fragments used to make transcriptional reporters. (A) Each <i>mgrA</i> promoter was independently cloned upstream of a promoterless copy of GFP in plasmid pCM11. Expression from the upstream promoter <i>mgrA</i> P2 (left) and downstream <i>mgrA</i> P1 (right) was assessed in the WT strain LAC (black) and the <i>arlRS</i> mutant (blue). (B) Western blot showing ArlR and MgrA protein levels at various time points (hours). (D) Quantification of MgrA protein levels in LAC (black, solid line) and the <i>arlRS</i> mutant (blue, solid line), and growth curves of the same strains (dotted lines). Quantification is representative of three separate experiments...
<p>(A) Schematic representation of the mutant <i>nadA</i> promoter variants (based on the MC58 <i>na...
<p>The Luc reporters driven by the full-length MGARP promoter (−3 kb) were transfected into HEK-293T...
<p>GFP reporter constructs were generated to assess the ability of sequences of <i>mdr1a</i> cDNA to...
<p>LAC WT, <i>arlRS</i>, and <i>mgrA</i> mutants contained either the empty vector or plasmids for c...
<p>(A) The <i>sraP</i> promoter region, showing the two putative transcription start sites (marked w...
<p>(A) Schematic drawings showing the two sites of interaction in the RsaA-<i>mgr</i>A complex. The ...
<p>A. Promoter analysis comparing the −3 kb upstream region of the MGARP gene between three species ...
<p><b>(A)</b> Staining of ARs produced by UW136 and U136::pALA8a strains, transformed with plasmid P...
<p>(A) Electrophoretic mobility shift assays carried out with a DNA fragment carrying the <i>pbgP</i...
<p>(A-B) NIH-3T3 cells stably expressing the indicated PML/RARA mutants were treated or not with 10<...
<p>(A–D) mRNA levels of the PmrA-activated <i>pbgP</i> (A, C) and <i>pmrC</i> (B, D) genes from isog...
<p>(A) Abundance of ectopically expressed PigR-V as analyzed by Western blot. (<i>Upper</i>) Western...
<p>(A) The GFP coding region was inserted between actin15 promoter (A15P) and actin8 terminator (A8T...
<p>(A) Schematic presentation of the GFP reporter constructs. The GFP coding region was inserted bet...
<p>ChIP was performed as described in the <a href="http://www.plosone.org/article/info:doi/10.1371/j...
<p>(A) Schematic representation of the mutant <i>nadA</i> promoter variants (based on the MC58 <i>na...
<p>The Luc reporters driven by the full-length MGARP promoter (−3 kb) were transfected into HEK-293T...
<p>GFP reporter constructs were generated to assess the ability of sequences of <i>mdr1a</i> cDNA to...
<p>LAC WT, <i>arlRS</i>, and <i>mgrA</i> mutants contained either the empty vector or plasmids for c...
<p>(A) The <i>sraP</i> promoter region, showing the two putative transcription start sites (marked w...
<p>(A) Schematic drawings showing the two sites of interaction in the RsaA-<i>mgr</i>A complex. The ...
<p>A. Promoter analysis comparing the −3 kb upstream region of the MGARP gene between three species ...
<p><b>(A)</b> Staining of ARs produced by UW136 and U136::pALA8a strains, transformed with plasmid P...
<p>(A) Electrophoretic mobility shift assays carried out with a DNA fragment carrying the <i>pbgP</i...
<p>(A-B) NIH-3T3 cells stably expressing the indicated PML/RARA mutants were treated or not with 10<...
<p>(A–D) mRNA levels of the PmrA-activated <i>pbgP</i> (A, C) and <i>pmrC</i> (B, D) genes from isog...
<p>(A) Abundance of ectopically expressed PigR-V as analyzed by Western blot. (<i>Upper</i>) Western...
<p>(A) The GFP coding region was inserted between actin15 promoter (A15P) and actin8 terminator (A8T...
<p>(A) Schematic presentation of the GFP reporter constructs. The GFP coding region was inserted bet...
<p>ChIP was performed as described in the <a href="http://www.plosone.org/article/info:doi/10.1371/j...
<p>(A) Schematic representation of the mutant <i>nadA</i> promoter variants (based on the MC58 <i>na...
<p>The Luc reporters driven by the full-length MGARP promoter (−3 kb) were transfected into HEK-293T...
<p>GFP reporter constructs were generated to assess the ability of sequences of <i>mdr1a</i> cDNA to...