Seedlings of the rubber tree clone RRIM600 after curative treatments with water (A), Colletotrichum alone (B), P. macrosporus-Isolate 37/06 (C), C. eragrostidi-Isolate 47/06 (D), M. levispora-Isolate 33/08 (E), and M. roridum-Isolate 03/10 (F).

Seedlings of the rubber tree clone RRIM600 after curative treatments with water (A), Colletotrichum alone (B), P. macrosporus-Isolate 37/06 (C), C. eragrostidi-Isolate 47/06 (D), M. levispora-Isolate 33/08 (E), and M. roridum-Isolate 03/10 (F).

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Anthracnose, caused by fungi of the genus Colletotrichum, is present in the main areas where rubber trees (Hevea brasiliensis) are planted. Thus, considering that biological agents can be an alternative for disease control, the present study aimed to carry out initial studies to investigate the response of rubber tree seedlings inoculated with Coll...

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... Differently from their response to powdery mildew, except for HbPAL3 and HbPAL6 with no change in expression, all other HbPALs were down-regulated in anthracnose-infected leaves. Bergamini Lopes et al. [40] showed that the activity of PAL was enhanced after treatments that strengthened anthracnose resistance in rubber trees. Therefore, we speculate that the susceptibility to anthracnose may be related to the decrease in HbPAL expression in the rubber tree. ...
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The majority of the world’s natural rubber comes from the rubber tree (Hevea brasiliensis). As a key enzyme for synthesizing phenylpropanoid compounds, phenylalanine ammonia-lyase (PAL) has a critical role in plant satisfactory growth and environmental adaptation. To clarify the characteristics of rubber tree PAL family genes, a genome-wide characterization of rubber tree PALs was conducted in this study. Eight PAL genes (HbPAL1-HbPAL8), which spread over chromosomes 3, 7, 8, 10, 12, 13, 14, 16, and 18, were found to be present in the genome of H. brasiliensis. Phylogenetic analysis classified HbPALs into groups I and II, and the group I HbPALs (HbPAL1-HbPAL6) displayed similar conserved motif compositions and gene architectures. Tissue expression patterns of HbPALs quantified by quantitative real-time PCR (qPCR) proved that distinct HbPALs exhibited varying tissue expression patterns. The HbPAL promoters contained a plethora of cis-acting elements that responded to hormones and stress, and the qPCR analysis demonstrated that abiotic stressors like cold, drought, salt, and H2O2-induced oxidative stress, as well as hormones like salicylic acid, abscisic acid, ethylene, and methyl jasmonate, controlled the expression of HbPALs. The majority of HbPALs were also regulated by powdery mildew, anthracnose, and Corynespora leaf fall disease infection. In addition, HbPAL1, HbPAL4, and HbPAL7 were significantly up-regulated in the bark of tapping panel dryness rubber trees relative to that of healthy trees. Our results provide a thorough comprehension of the characteristics of HbPAL genes and set the groundwork for further investigation of the biological functions of HbPALs in rubber trees.