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Salamzade, R. A.

Publications and source records attributed to Salamzade, R. A..

2 recordsLinked to original sources

bofasa enables high-quality orthology inference across diverse multi-species bacterial genome sets

Bacterial species can be separated by billions of years of evolution. However, studies of such ancient relationships often rely on methods developed for eukaryotes, which are less diverse. Such methods can regard instances of horizontal gene transfer as contamination, rely heavily on a species phylogeny when partitioning paralogs, and fail to account for the multi-domain architectures of some genes. Here, we introduce, showcase, and benchmark bofasa, a software for high-quality and automated inference of ortholog groups across distantly related bacterial species. bofasa employs a recursive algorithm to split coarse homolog groups into paralogous subsets and first establishes domain-level ortholog groups prior to assessing evolutionary relationships between entire proteins. In comparison to other methods commonly used for multi-species bacterial comparative genomics, bofasa is substantially more conservative in predicting orthology yet can often recover the largest single-copy core genome. Beyond orthology inference, the software also features several additional utility functionalities, including assessment of which ortholog groups are commonly found on mobile genetic elements or possess variable genomic contexts.

microbiology↗

Complex multicellularity linked with expanded chemical arsenals in microbes

Single-celled microorganisms evolving to form cooperative multicellular units represents a key innovation in the history of life. Multicellularity is required for cell differentiation and, as such, is critical to the emergence of biological complexity. Here, we propose and find support for our hypothesis that multicellularity facilitated massive expansions in the biosynthetic potential to produce specialized metabolites across microbial life. Our systematic characterization of biosynthetic gene clusters (BGCs) across bacteria confirms that most taxa have limited predicted potential to produce natural products. In contrast with primarily unicellular lineages, we show that the origins of biosynthetic expansion in Actinomycetota, Cyanobacteriota, and Myxococcota coincide with independent origins of multicellular structures such as mycelia, filaments, and fruiting bodies. Further, we reveal that the two primary origins of expansions in specialized metabolism for fungi, corresponding to the Pezizomycotina and Agaricomycetes, similarly coincide with the emergence of complex multicellularity and fruiting body formation as well as mechanisms for self-identification during haplontic life cycles. Interestingly, all five of the biosynthetically talented multicellular microbial lineages are concomitantly enriched in carbohydrate utilization enzymes, suggesting that ancient chemical innovations have been further shaped by catabolic processes. Intraspecific cooperation shaping the evolution of specialized metabolism further informs our understanding of the major transitions in life and will help guide efforts to discover new antimicrobial compounds to counter the emergence of antibiotic resistance.

evolutionary biology↗