2006
DOI: 10.1016/j.jplph.2005.05.001
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Molecular cloning and expression analysis of the replacement histone H3 gene of Italian ryegrass (Lolium multiflorum)

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Cited by 6 publications
(6 citation statements)
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References 28 publications
(28 reference statements)
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“…We found that NgRDR1 cannot be induced by the bacterium Ralstonia solanacearum. Similar results were reported in Arabidopsis, where the T-DNA insertion 36 mutant for AtRDR1 inoculated by bacterium worked similarly to the wild type [43]. However, NgRDR1 can be induced by some fungi and viruses.…”
Section: Discussionsupporting
confidence: 84%
See 1 more Smart Citation
“…We found that NgRDR1 cannot be induced by the bacterium Ralstonia solanacearum. Similar results were reported in Arabidopsis, where the T-DNA insertion 36 mutant for AtRDR1 inoculated by bacterium worked similarly to the wild type [43]. However, NgRDR1 can be induced by some fungi and viruses.…”
Section: Discussionsupporting
confidence: 84%
“…Firstly, the Pro1 and Pro2 primers were designed in accordance with the 5 0 end of the genomic sequence and the adaptor-PCR was performed as described previously [37]. Then, we designed primers TF1, TF2, TR1 and TR2 based on the cloned sequence and used the inverse polymerase chain reaction (IPCR) to clone the residual region [36]. At last, the whole obtained sequence of the 5 0 -flanking region was used to design the specific primers Fp and Rp for direct PCR amplification from N. glutinosa genomic DNA.…”
Section: Cis-elementmentioning
confidence: 99%
“…Since expression levels of ZBD1 in the transgenic plants seemed to be low, other promoters should be investigated. The multiple-stress-inducible promoter IRH3prm, which is the 5′-regulatory sequence of a replacement histone H3 gene of Italian ryegrass (Takahashi et al 2006), is a possible candidate.…”
Section: Discussionmentioning
confidence: 99%
“…One microgram genomic DNA was digested individually at 37°C for 24 h with 7 restriction endonucleases (BglII, EcoRI, EcoRV, HaeIII, HindIII, XbaI and VspI), respectively. The purification and circularization of the digested DNA samples were performed as described previously (Takahashi et al 2006). For cloning of the full-length GhMPK2 promoter, the circularized DNA digested with BglII was used as template in IPCR, employing two pairs of nested primers: P1 and P2, and P3 and P4.…”
Section: Vector Construction and Genetic Transformationmentioning
confidence: 99%