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Gunther, L.

Publications and source records attributed to Gunther, L..

2 recordsLinked to original sources

ABCC10 roles in plant development and the transport of indole-3-butyric acid

Proper spatiotemporal distribution of the phytohormone auxin throughout plant tissues mediates a variety of developmental processes. Auxin levels are tightly regulated via de novo synthesis, transport, and conversion from its conjugated forms and precursors. These levels can be regulated through conversion of the auxin precursor, indole 3-butyric acid (IBA), into the active auxin, indole-3-acetic acid (IAA), in a peroxisomal {beta}-oxidation process. Defects in IBA-to-IAA conversion cause multiple developmental defects in Arabidopsis, demonstrating IBA-derived IAA is physiologically important to the active auxin pool. Similar to IAA, transport of IBA modulates development. However, the mechanisms governing transport of this molecule remain largely unknown. Here, we identify a mutation in the ABCC10 gene of Arabidopsis that suppresses the abcg36 hypersensitivity to IBA and its synthetic analog, 2,4-dichlorophenoxy butyric acid (2,4-DB) and the abcg36 hyperaccumulation of [3H]-IBA. We found that ABCC10 acts as a direct vacuolar transporter of IBA. Further, ABCC10 is necessary for proper development of the root apical meristem and leaf tissue. Our findings uncover a previously uncharacterized method of IBA transport that regulates aspects of plant development.

plant biology↗

Genome Methylation Predicts Age and Longevity of Bats

Exceptionally long-lived species, including many bats, rarely show overt signs of aging, making it difficult to determine why species differ in lifespan. Here, we use DNA methylation (DNAm) profiles from 712 known-age bats, representing 26 species, to identify epigenetic changes associated with age and longevity. We demonstrate that DNAm accurately predicts chronological age. Across species, longevity is negatively associated with the rate of DNAm change at age-associated sites. Furthermore, analysis of several bat genomes reveals that hypermethylated age- and longevity-associated sites are disproportionately located in promoter regions of key transcription factors (TF) and enriched for histone and chromatin features associated with transcriptional regulation. Predicted TF binding site motifs and enrichment analyses indicate that age-related methylation change is influenced by developmental processes, while longevity-related DNAm change is associated with innate immunity or tumorigenesis genes, suggesting that bat longevity results from augmented immune response and cancer suppression.

genomics↗