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The objective of this study was to determine the effects of four phenol–formaldehyde (PF) resin treatments with different molecular weights at four different concentrations (5, 10, 15, and 20%) in treated beech wood. The mechanical properties of untreated and treated beech wood were evaluated. After impregnation with PF resin, all modified beech wood at all PF resin concentrations exhibited an increase in weight percent gain compared with that in untreated beech samples. PF resins with lower molecular weights more easily penetrate the wood cell wall, leading to increased bulking of the wood structure, which in turn improves the dimensional stability of the wood. The PF resin treatment with a molecular weight of 305 g/mol showed better impregnation ability than that of the other PF resins. The impact bending strength of PF-treated wood was considerably reduced because PF-cured resins formed inside the wood and are rigid and brittle. Additionally, PF resin treatments at all concentrations decreased the modulus of elasticity of the wood. Scanning electron microscopy and light microscopy revealed that the PF resins were comparatively well fixed in the wood samples. The results indicate that the large molecular weight PF resins are more uniformly distributed in the fiber lumens.

The effects of introns, especially the first intron, on the regulation of gene expression remains unclear. Therefore, the objective of the present study was to investigate the transcriptional regulatory function of intron 1 on the chicken growth hormone (cGH) gene in the rat pituitary tumor cell line (GH4-C1). Transient transfection using first-intron-inserted cGH complete coding sequences (CDSs) and non-intron-inserted cGH CDS plasmids, quantitative RT-PCR (qRT-PCR) and western blot assays were used to detect the expression of cGH. The reporter gene assay was also used to investigate the effect of a series of fragments in the first intron of cGH on gene expression in GH4-C1. All of the results revealed that a 200-bp fragment located in the +485/+684 region of intron 1 was essential for repressing the expression of cGH. Further informatics analysis showed that there was a cluster of 13 transcriptional factor binding sites (TFBSs) in the +485/+684 region of the cGH intron 1. Disruption of a glucocorticoid response-like element (the 19-nucleotide sequence 5′-AGGCTTGACAGTGACCTCC-3′) containing a T-box motif (TGACCT) located within this DNA fragment increased the expression of the reporter gene in GH4-C1. In addition, an electrophoretic mobility shift assay (EMSA) revealed a glucocorticoid receptor (GR) protein of rat binding to the glucocorticoid response-like element. Together, these results indicate that there is a negative glucocorticoid response-like element (nGRE) located in the +591/+609 region within the first intron of cGH, which is essential for the down-regulation of cGH expression.