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Hsu, H.-W.

Publications and source records attributed to Hsu, H.-W..

2 recordsLinked to original sources

Temperature dependence of pollen germination in Douglas-fir (Pseudotsuga menziesii): A machine learning-based detection of pollen viability from microscopic images

Background and Aims: Pollen germination and tube growth are critical stages of plant reproduction that are highly sensitive to temperature but remain labor-intensive to quantify. This study aimed to develop a deep learning-based approach for pollen phenotyping and to characterize the temperature dependence of pollen germination and elongation in Douglas-fir (Pseudotsuga menziesii). Methods: A convolutional neural network (CNN) was trained to segment pollen grains and classify germination status from microscopic images. Germination percentage and pollen length were quantified across a range of incubation temperatures from 5 to 40{degrees}C. Gamma functions were fitted to temperature response curves to estimate the optimal temperatures for pollen germination and elongation among Douglas-fir populations collected across an elevational gradient. Key Results: The CNN achieved high segmentation accuracy (intersection over union = 0.846), accurately distinguishing pollen grains from the background but showing moderate accuracy in separating germinated from ungerminated pollen during early elongation. Both pollen germination and elongation exhibited bell-shaped temperature response curves with distinct thermal optima. Pollen elongation consistently reached its optimum at higher temperatures than pollen germination. Estimated optimal temperatures fell within a narrow range, approximately 19 to 23{degrees}C. No significant relationship was detected between elevation and thermal optima, although some higher-elevation populations exhibited lower optimal temperatures. Comparisons with previous analyses of three western North American conifers showed that each species occupied a distinct reproductive thermal niche corresponding to the spring temperatures of its native habitat. Conclusions: Deep learning provides an efficient approach for high-throughput quantification of pollen germination and elongation from microscopic images. The narrow thermal range for reproductive performance suggests that Douglas-fir pollen is sensitive to temperature variation and that warming climates may alter reproductive success. These findings improve our understanding of the thermal sensitivity of conifer reproduction and provide a scalable framework for assessing impacts of climate warming on forest regeneration.

ecology↗

N6-methyladenosine regulates Influenza A virus mRNA stability yet is rarely found on genomic RNA

Previous studies have found widespread N6-methyladenosine (m6A methylation) on all forms of Influenza A virus (IAV) RNA, with m6A found critical for viral replication, pathogenicity as well as viral RNA packaging. Here we applied the latest quantitative technologies to revisit the methylation landscape on the anti-sense genomic RNA of IAV. Unexpectedly, upon Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS) analysis of IAV virion -extracted genomic RNA, we detected very little m6A regardless of production from human cells or chicken eggs. Concordantly, Nanopore direct RNA sequencing also detected an overall low occurrence and stoichiometry (generally <5%) of m6A across all viral genomic RNA segments, compared with abundant m6A sites on viral mRNAs at ~20-30% m6A. Cross validation with glyoxal- and nitrite-mediated deamination of unmethylated adenosines (GLORI) confirmed multiple m6A sites on viral mRNA yet very few m6A on the genomic RNA. This paucity of m6A on genomic RNA makes it unlikely that m6A contributes to viral RNA packaging. Knockdown or pharmacological inhibition of the m6A methyltransferase METTL3 as well as the reader protein YTHDF2 both reduced viral mRNA levels and infectious viral particle production, with YTHDF2 promoting viral mRNA stability. Thus, the presence of m6A on IAV transcripts is indeed proviral, yet it is the mRNAs instead of genomic RNAs that are methylated at functionally relevant levels. Lastly, we provide proof of concept that a METTL3 small molecule inhibitor can be antiviral, and propose that m6A-targeted antivirals would mainly impact the intracellular gene expression phase of IAV replication.

microbiology↗