A gene designated jadI from the jadomycin B producer Streptomyces
venezuelae has homology to
the tetracenomycin pathway tcmI gene and encodes a putative cyclase for angucyclinone biosynthesis. Expression
in Streptomyces lividans of a jadomycin (jad) gene cassette composed of the minimal polyketide synthase
(PKS, jadABC), a cyclase (jadD), a ketoreductase (jadE), and jadI leads to production of several yellow
compounds in liquid culture. Rabelomycin (1), a known angucyclinone, results from dehydration and oxidation
of a new product, UWM6, isolated from the culture extracts. Characterization of UWM6 by UV, MS, and
NMR analyses revealed a new angucyclinone structure, 4-hydroxy-12bH-12-deoxyrabelomycin. Production
of these angucyclinones occurs only when jadI is present in the cassette, suggesting an essential cyclase
phenotype for this gene. Engineered replacement of jadI in the jad cassette with the tcmI cyclase gene, and
similar replacement of tcmI in a functional tcm PKS cassette with jadI, leads to the same set of aromatic
decapolyketides produced by either cassette in the absence of jadI. From these results we conclude that both
cyclases are nonfunctional out of their normal context.
The molecular mechanism underlying brain regeneration in vertebrates remains elusive. We performed spatial enhanced resolution omics sequencing (Stereo-seq) to capture spatially resolved single-cell transcriptomes of axolotl telencephalon sections during development and regeneration. Annotated cell types exhibited distinct spatial distribution, molecular features, and functions. We identified an injury-induced ependymoglial cell cluster at the wound site as a progenitor cell population for the potential replenishment of lost neurons, through a cell state transition process resembling neurogenesis during development. Transcriptome comparisons indicated that these induced cells may originate from local resident ependymoglial cells. We further uncovered spatially defined neurons at the lesion site that may regress to an immature neuron–like state. Our work establishes spatial transcriptome profiles of an anamniote tetrapod brain and decodes potential neurogenesis from ependymoglial cells for development and regeneration, thus providing mechanistic insights into vertebrate brain regeneration.
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