A Complete Genome for the Common Marmoset

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Authors: Prajna Hebbar, Tamara Potapova, Hailey Loucks, Karina Ray, Murillo Fernando Rodrigues, Fedor Ryabov, Joanna Malukiewicz, DongAhn Yoo, Leonardo Gomes de Lima, Annat Haber, Sonal Kumar, Swati Banerjee
+30 more Matthew Borchers, Gage H. Garcia, Joshua M.V. Gardner, Stephanie Hachem, Harrison D. Heath, Seung-Kwon Ha, Mira Mastoras, Brandy M. McNulty, Julian Menendez, Katherine M. Munson, Karol Pál, Jungeun Park, Simon Ploesch, Christian Roos, William Seligmann, Valery A. Shepelev, Catrina Spruce, Ivo Violich, Lutz Walter, Kateryna D. Makova, Amantha Thathiah, Stacey J. Sukoff Rizzo, Afonso C. Silva, Gregory W. Carter, Karen H. Miga, Evan E. Eichler, Donald F. Conrad, Jennifer L. Gerton, Ivan A. Alexandrov, Benedict Paten
Cited by: 1
References: 71

Abstract

The common marmoset is a New World monkey (NWM) commonly used as a model organism to investigate questions in primate evolution and human disease, including Alzheimer's and other neurodegenerative diseases, as well as neuropsychiatric disorders. Here we present the first telomere-to-telomere (T2T) reference genome for the common marmoset, adding over 88 Mb of sequence and resolving challenging genomic regions. An additional near-T2T assembly from a second unrelated individual yields a total of four high-quality haplotypes for analysis. The improved contiguity and accuracy of these assemblies enable unprecedented insights into complex and rapidly evolving genomic regions such as centromeres, sex chromosomes, ribosomal DNA (rDNA) structure, and the major histocompatibility complex (MHC). We fully resolved all marmoset centromeres, uncovering dimeric alpha satellites with chromosomal specificity and stratified inactive layers documenting ancestral centromere turnover. We assembled six acrocentric autosomes with gene-poor, satellite-rich short arms and provide evidence that most of them can harbor rDNA and all of them share large pseudo-homologous regions (PHRs). The Y chromosome, but not the X chromosome, carries active rDNA and PHRs, and the rDNA copy number is sexually dimorphic. Chromosomes that share PHRs also share closely related centromeric satellite DNA, supporting a model of ongoing recombinational exchange between heterologous chromosomes facilitated by rDNA. We discovered multiple novel, marmoset-specific MHC genes that are predicted to protect against pathogens encountered in its environment. Leveraging this complete reference, we further identified over 500 transcribed genes with transcript models or expansions specific to the marmoset lineage. Together with additional long-read marmoset assemblies, these genomes were used to construct a marmoset pangenome, providing a robust reference framework for short-read mapping across diverse individuals. This resource will improve the utility of the common marmoset as a biomedical model organism and fill key gaps in our understanding of primate evolution.

Fields of Study & Subjects

Chromosomal and Genetic Variations Genomic variations and chromosomal abnormalities Genomics and Phylogenetic Studies

Publication details

Journal / source
bioRxiv (Cold Spring Harbor Laboratory)
Publisher
openRxiv
Publication date
26 March 2026
Language
EN
Document type
Preprint