Evidence map›Paper›PMID 42230317›Full record

ArticleGenome biology and evolution2026

Conservation of Human IgSF Proteins Throughout Eukaryotic Evolution.

Steven Grudman, Andras Fiser

Abstract read
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Article in Genome biology and evolution, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Steven GrudmanDepartment of Systems & Computational Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.ORCID 0009-0002-2504-9575
Andras FiserDepartment of Systems & Computational Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.ORCID 0000-0003-0085-5335

Funding

Molecular basis of recognition in the Immunological SynapseR35GM136357 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI FISER, ANDRAS · 2020 to 2024
$2.7M
NIGMS NIH HHS R35 GM136357
6 · The paper itself

Abstract

The human immunoglobulin superfamily (IgSF) encompasses hundreds of proteins involved in cell-cell adhesion, neural connectivity, junctional organization, and immune regulation, with many serving as key checkpoint proteins. To elucidate the evolutionary history of human IgSF members, we systematically analyzed all available eukaryotic reference genomes to determine when each IgSF subfamily first appeared. The human IgSF was partitioned into six major evolutionary timeframes: Metazoa, Vertebrata, Gnathostomata, Tetrapoda, Amniota, and Mammalia. Although proteins were grouped solely by their conservation across eukaryotes, their biological functions clustered naturally, reflecting how new physiological systems create selective pressures that drive the appearance, retention, and diversification of protein architectures suited to those functions. Conservation and functional analyses indicate that human IgSF members arising in tetrapods and amniotes primary regulate the strength and duration of immune responses and form many of the critical components of the immune synapse, while IgSF genes that appear first in mammals have evolved to fine-tune immune activation thresholds to support maternal-fetal tolerance. Case studies are provided to illustrate three key evolutionary themes: (i) highly conserved yet catalytically inactive proteins retain essential regulatory functions, (ii) functional convergence among evolutionarily distinct IgSF families, and (iii) compensatory evolution within adaptive immunity following a lineage-specific loss of an IgSF member. Together, these findings establish an evolutionary framework for organizing the human IgSF by both ancestry and function, providing a foundation for assessing IgSF importance. Notably, this study facilitates the identification of conserved but understudied proteins that emerged alongside the development of the adaptive immune system, highlighting them as promising candidates for future experimental investigation.

Indexed as

Evolution, MolecularImmunoglobulinsAnimalsConserved SequenceHumansPhylogenyImmunoglobulinsevolution of adaptive immune systemevolution of co-stimulatory immune receptorsextracellular IgSFgnathostomes

Identifiers

PMID42230317
PMCPMC13262535

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