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Biology subjects

Saturne, M.

Publications and source records attributed to Saturne, M..

2 recordsLinked to original sources

Autosomal dominant CDC45 deficiency with allelic expression bias causes a novel genetic disease of the immune system

Here we describe a damaging heterozygous variant in CDC45 in an individual with common variable immunodeficiency (CVID) and recurrent viral infections. This individual has variably decreased number of circulating NK cells, disruption in the ratio of CD56bright to CD56dim cells, and consistently decreased NK cell function. Interestingly, the inherited CDC45 variant is also present in a sibling with less severe clinical manifestations; we determined that allelic bias of the damaging allele accounts for this differential expressivity. As previously reported for other helicase variants that cause inborn errors of immunity (IEI), we found cell cycle defects in immune cells from the proband that lead to reduced survival of NK cells. Together, these findings link another member of the core replicative helicase complex to inborn errors of immunity and highlight the sensitivity of NK cells to these variants. They also define another case of allelic bias contributing to variable expressivity of an IEI gene.

immunology↗

Single-cell analysis identifies a key role for Hhip in murine coronal suture development

Craniofacial development depends on proper formation and maintenance of sutures between adjacent bones of the skull. In sutures, bone growth occurs at the edge of each bone, and suture mesenchyme maintains the separation between them. We performed single-cell RNA-seq analyses of the embryonic, murine coronal suture. Analyzing replicate libraries at E16.5 and E18.5, we identified 14 cell populations. Seven populations at E16.5 and nine at E18.5 comprised the suture mesenchyme, osteogenic cells, and associated populations. Through an integrated analysis with bulk RNA-seq data, we found a distinct coronal suture mesenchyme population compared to other neurocranial sutures, marked by expression of Hhip, an inhibitor of hedgehog signaling. We found that at E18.5, Hhip-/- coronal osteogenic fronts are closely apposed and suture mesenchyme is depleted, demonstrating that Hhip is required for coronal suture development. Our transcriptomic approach provides a rich resource for insight into normal and abnormal development.

developmental biology↗