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Trim66's paternal deficiency causes intrauterine overgrowth. | LitMetric

Trim66's paternal deficiency causes intrauterine overgrowth.

Life Sci Alliance

Epigenetics and Neurobiology Unit, EMBL Rome, European Molecular Biology Laboratory, Monterotondo, Italy

Published: July 2024

The tripartite motif-containing protein 66 (TRIM66, also known as TIF1-delta) is a PHD-Bromo-containing protein primarily expressed in post-meiotic male germ cells known as spermatids. Biophysical assays showed that the TRIM66 PHD-Bromodomain binds to H3 N-terminus only when lysine 4 is unmethylated. We addressed TRIM66's role in reproduction by loss-of-function genetics in the mouse. Males homozygous for mutations produced functional spermatozoa. Round spermatids lacking TRIM66 up-regulated a network of genes involved in histone acetylation and H3K4 methylation. Profiling of H3K4me3 patterns in the sperm produced by the -null mutant showed minor alterations below statistical significance. Unexpectedly, -null males, but not females, sired pups overweight at birth, hence revealing that mutations cause a paternal effect phenotype.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11077763PMC
http://dx.doi.org/10.26508/lsa.202302512DOI Listing

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