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Madeja, Z. E.

Publications and source records attributed to Madeja, Z. E..

2 recordsLinked to original sources

Multi-omic screening identifies RBMXL3 as a primate-specific RNA-binding protein and candidate regulator of RNA metabolism in human spermatogenesis

BackgroundRBMXL3 is a primate-specific gene localized on the X chromosome, which expression is detectable mainly in the male gonad. So far, very little is known about the RBMXL3 protein function and its molecular interactions. However, recent reports mention the RBMXL3 gene in the context of human spermatogenesis, cancer, and a breathing disorder that affects newborns. In this study, we investigate the RBMXL3s molecular network on a genome-wide scale using the human seminoma cell line (TCam-2) as a male germline in vitro model. MethodsBy using transcriptomic (RNA sequencing (RNA-seq) and enhanced crosslinking and immunoprecipitation (eCLIP)) and proteomic (Co-immunoprecipitation coupled with Mass Spectrometry, (Co-IP-MS)) approaches we show RBMXL3 importance in RNA metabolism. Additionally, Western Blot, qRT-PCR, immunostaining, and confocal imaging were used in order to investigate the function of RBMXL3. Finally, we used a plasmid-based L1 retrotransposition assay to demonstrate the suppressive effect of RBMXL3 on human Long Interspersed Nuclear Element-1 (LINE-1, L1) retrotransposition. ResultsOur RNA-seq data show that RBMXL3 expression drives gene expression changes and influence alternative splicing in human cells. Moreover, by performing eCLIP we provide a proof that RBMXL3 binds to a wide range of RNA transcripts. Additionally, we confirmed the nuclear localization of RBMXL3 in TCam-2 cells and its presence in spermatogonia and spermatocytes within the human testis. Finally, we report for the first time that RBMXL3 restricts human LINE-1 retrotransposition. ConclusionsOur findings for the first time identify primate-specific RBMXL3 protein as a new upstream regulator of RNA metabolism, characterized by broad RNA-binding activity in human TCam-2 cells. Finally, we show that RBMXL3 expression heavily reduces LINE-1 retrotransposition in human cells, underlying RBMXL3 importance in maintaining genome integrity. Our data suggest that RBMXL3 may contribute to the regulation of transcriptome dynamics in male germ cells, while its broader functional implications remain to be determined. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=56 SRC="FIGDIR/small/677621v3_ufig1.gif" ALT="Figure 1"> View larger version (21K): org.highwire.dtl.DTLVardef@8bf116org.highwire.dtl.DTLVardef@180fe82org.highwire.dtl.DTLVardef@1c52960org.highwire.dtl.DTLVardef@11f7519_HPS_FORMAT_FIGEXP M_FIG C_FIG Created with BioRender.com

cell biology↗

Stage-sensitive potential of isolated rabbit ICM to differentiate into extraembryonic lineages

In the course of mammalian development initial state of totipotency must be lost to allow acquisition of specific cell fates. The first differentiation event results in the formation of trophectoderm (TE) and the inner cell mass (ICM). In the mouse embryo the cell fate of these two compartments is set quickly after formation of a blastocyst. However, recent reports suggest that plasticity of these two lineages might be extended in species other than the mouse. Here we investigated how the cellular plasticity of early mammalian embryos relates to developmental time scale and changes in gene expression using rabbit isolated ICMs. We studied the dynamics of rabbit blastocyst formation using time-lapse imaging and identified GATA3 as an early marker of rabbit TE and CDX2 as a marker of fully formed TE. We then analysed developmental potential of rabbit ICMs isolated by immunosurgery and subsequently cultured in vitro. ICMs originating from early- to mid-blastocyst stage embryos are able to re-form a blastocyst-like structure, with a functional TE, and an ICM containing both SOX2-positive epiblast cells and SOX17-positive primitive endoderm cells. We further observed that rabbit ICMs isolated from later blastocyst stages lose the ability for TE specification, instead forming a halo-like cavity with an outer layer of SOX17-positive cells. Our data indicate that in mammalian embryos the potential for TE differentiation gives way to formation of a different type of extraembryonic epithelial layer, suggesting potential common mechanism of pluripotency restriction between eutherian mammals.

developmental biology↗