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Soham Dibyachintan

@sohamdibyachintan.bsky.social
136 followers 448 following 14 posts

Ph.D. student Landry Lab gene duplication, cell signaling, protein evolution, full time member of the APOYG cult

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Reposted by Soham Dibyachintan
Nature Reviews Genetics @natrevgenet.nature.com · 01/07/2026
Our Review is free to read here: rdcu.be/e4CYK
rdcu.be
Evolutionary causes and consequences of gene duplication
Nature Reviews Genetics - Gene duplication is a key evolutionary mechanism, as initially redundant paralogues diverge over time. The authors review how adaptive and non-adaptive forces influence...
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Reposted by Soham Dibyachintan
Nature Reviews Genetics @natrevgenet.nature.com · 09/03/2026
FYI: New online! Evolutionary causes and consequences of gene duplication
dlvr.it
Evolutionary causes and consequences of gene duplication
Nature Reviews Genetics, Published online: 16 February 2026; doi:10.1038/s41576-026-00935-5Gene duplication is a key evolutionary mechanism, as initially redundant paralogues diverge over time. The authors review how adaptive and non-adaptive forces influence the evolutionary fates of gene duplicates, highlighting the importance of function–fitness relationships and gene expression dynamics.
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Reposted by Soham Dibyachintan
Stephen Turner @stephenturner.us · 21/02/2026
Evolutionary causes and consequences of gene duplication www.nature.com/articles/s41... 🧬💻🧪 (🔓 rdcu.be/e4CYK)
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Reposted by Soham Dibyachintan
Soham Dibyachintan @sohamdibyachintan.bsky.social · 16/02/2026
Our new review about the evolutionary causes and consequences of gene duplication is out!!! We delve into the various adaptive and non-adaptive forces which shape the fate of gene duplicates uncovered across the last decade through cutting edge experimental and computational techniques
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 16/02/2026
Our new review about the evolutionary causes and consequences of gene duplication is out!!! We delve into the various adaptive and non-adaptive forces which shape the fate of gene duplicates uncovered across the last decade through cutting edge experimental and computational techniques
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Reposted by Soham Dibyachintan
Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
How does cryptic genetic variation influence the long-term fate of gene duplicates (paralogs)? Our new study addresses this question by dissecting the evolutionary potential of redundant myosin paralogs in yeast nature.com/articles/s41... (1/12)
nature.com
Cryptic genetic variation shapes the fate of gene duplicates in a protein interaction network - Nature Communications
Over time, paralogous genes accumulate changes in their sequences that do not affect their function, which is called cryptic variation. Using paralogous myosins, this study shows how cryptic variation...
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Reposted by Soham Dibyachintan
Vaughn Cooper @vscooper.micropopbio.org · 02/06/2025
Fantastic study of the evolution of epistasis in paralogs!
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
n summary: Cryptic genetic variation — both regulatory and coding variation— biases the future of redundant gene duplicates by altering the effects of new mutations (12/12) #evolution #epistasis #genetics
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
Our work underscores the importance of historical contingency in molecular evolution. Redundant paralogs are not evolutionary blank slates — they are subtly shaped by past substitutions and regulatory shifts that influence their future evolution (11/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
Thus, cryptic divergence alters the functional landscape of gene duplicates. A mutation that is benign in one paralog can be deleterious in the other, thereby shaping asymmetric evolutionary trajectories and biasing the potential for subfunctionalization or loss of one of the paralogs (10/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
To explore the origin of this divergence in effects, we introduced historical substitutions from one paralog into the other individually and in pairs. We found strong evidence of pairwise epistasis: certain mutations only impacted function in specific sequence contexts (9/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
Approximately 15% of mutations showed divergence in functional effects between domains, which we refer to as contingent mutations, even when both domains were expressed at the same levels. These mutations were enriched at solvent-exposed, consistent with roles in binding specificity (8/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
Not all mutations were globally destabilizing for all interactions. Some selectively impaired binding to a single interaction partner, suggesting that such changes could lead to subfunctionalization — the partitioning of ancestral functions between paralogs (7/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
By swapping the SH3 domains between the two paralogs, we found that the expression level alone can modulate the severity of binding impairment. A mutation's impact is not fixed — it depends on the expression level of the protein in which it occurs (6/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
We found the divergence in functional effects arose from two main sources: 1. Regulatory divergence — MYO5 is more highly expressed than MYO3, buffering it against deleterious mutations 2. Sequence divergence — cryptic amino acid substitutions that modulate mutational effects via epistasis (5/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
We found that many mutations exhibited paralog-specific effects. Identical substitutions in the two SH3 domains led to divergent impacts on binding, demonstrating that even functionally redundant domains diverge in their evolutionary potential (4/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
We combined saturated mutagenesis and CRISPR with high-throughput phenotyping of SH3 domains of MYO3 and MYO5 in S. cerevisiae, introducing all possible single amino acid substitutions, and assessed how these variants affected binding to 8 biologically relevant protein interaction partners (3/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
Although paralogs like myosin-3 (MYO3) and myosin-5 (MYO5) often retain redundant functions, they gradually accumulate subtle changes in expression and sequence that do not immediately impact function, a phenomenon called cryptic divergence (2/12)
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 02/06/2025
How does cryptic genetic variation influence the long-term fate of gene duplicates (paralogs)? Our new study addresses this question by dissecting the evolutionary potential of redundant myosin paralogs in yeast nature.com/articles/s41... (1/12)
nature.com
Cryptic genetic variation shapes the fate of gene duplicates in a protein interaction network - Nature Communications
Over time, paralogous genes accumulate changes in their sequences that do not affect their function, which is called cryptic variation. Using paralogous myosins, this study shows how cryptic variation...
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Soham Dibyachintan @sohamdibyachintan.bsky.social · 10/11/2024
Welcome! Hi Harmit!!
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