Turner Lab
@lab-turner.bsky.social
300 followers 210 following 23 posts
Account of the Turner lab at the Francis Crick Institute in London. We study sex chromosomes and their impact on health and disease. Rotating curation by lab members. https://www.crick.ac.uk/research/labs/james-turner
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lab-turner.bsky.social
Paper alert! 🚨 Something new from us, and this time it's not sex chromosome related 😱 All led by @sermenchero.bsky.social who used the opossum as a model to understand developmental heterochrony. Transcriptional and morphological progression of dev programs are decoupled www.cell.com/developmenta...
Reposted by Turner Lab
jamiehackett.bsky.social
We are looking to take on an intern at EMBL Rome, for anyone interested in CRISPR and Epigenetics training.

The traineeship is 3-12-months, in Rome (Italy), should start by July, and is supervised by the outstanding @steliostsagkris.bsky.social.

#job #internship; see info below...
lab-turner.bsky.social
This project was a massive team effort, within our lab, with collaborators, and with help from @crick.ac.uk facilities @sermenchero.bsky.social @aureliencourtois.bsky.social and others not on Bluesky
lab-turner.bsky.social
In marsupials, X inactivation is imprinted, affecting the paternally-inherited X chromosome, and is thought to be regulated by the non-coding RNA RSX. When comparing sperm and oocytes at the RSX locus, we see a differentially methylated region, which might be a regulatory mechanism for imprinted XCI
lab-turner.bsky.social
Of course, we also dig into epigenetic regulation of X chromosome inactivation. The inactive X in adult marsupial cells adopts an unusual hypomethylated state – devoid of DNA methylation. Using our embryo data we show that the inactive X progressively loses methylation throughout early development
lab-turner.bsky.social
Our study suggests that a unique extra-embryonic methylation state is a conserved feature of mammals – and therefore is likely to be important for the evolution of the placenta
lab-turner.bsky.social
Secondly, after 5 days, DNA methylation drops, but does so largely in the extra-embryonic trophectoderm cells that will go to form the placenta, while remaining largely unchanged in the cells that give rise to the embryo proper
lab-turner.bsky.social
The paper provides two main important findings. Firstly, in contrast to mouse, early wiping of DNA methylation simply doesn’t happen in the marsupial embryos (up to day 5), with methylation levels remaining consistent during embryo genome activation and pluripotent stem cell formation
lab-turner.bsky.social
To address this question, we looked at the DNA methylation of marsupial embryos, which split from eutherian mammals 160 million years ago. By leveraging the more spaced out embryo development in marsupials we mapped changes in the epigenome to the processes described above
lab-turner.bsky.social
In eutherian (placental) mammals, the early embryo “wipes” its epigenome, but we don't know why. Many things happen early in placental mammalian embryos, and all in very quick succession: the embryo genome activates, pluripotent stem cells appear, and the placental precursor cells are formed
lab-turner.bsky.social
These well-defined cell lines provide a unique platform to investigate the role of sex as a biological variable across diverse cell types and to elucidate the impact of sex chromosome complement in human disease models 🧫🧬
lab-turner.bsky.social
We are excited to share our latest preprint led by Ruta Meleckyte and Waz Varsally! www.biorxiv.org/content/10.1... We generated a set of human isogenic induced pluripotent stem cells (hiPSCs) that are autosomally identical but differ in sex chromosome composition: XX, XY or monosomic X
A human induced pluripotent stem cell toolbox for studying sex chromosome effects
Sex chromosomes shape male (XY) - female (XX) differences in development and disease. These differences can be modelled in vitro by comparing XY and XX human induced pluripotent stem cells (hiPSCs). H...
www.biorxiv.org
Reposted by Turner Lab
yen-network.bsky.social
Registration and abstract submission for YEN 2025 is officially open!

We are looking forward to seeing you at the 17th Young Embryologist Network Conference on the 19th May 2025.

Attendence is FREE thanks to our amazing sponsors: @biologists.bsky.social @10xgenomics.bsky.social and Azenta.
lab-turner.bsky.social
This work was only possible because of the amazing facilities at @crick.ac.uk and our wonderful collaborators.
lab-turner.bsky.social
We generate a bulk and single nuclei RNAseq atlas of Y-gene KOs, identifying possible underlying molecular mechanisms causing spermatogenic defects. We see an interesting impact of Y genes on somatic cells of the testis
lab-turner.bsky.social
We make the equivalent of the human infertility AZFa deletion encompassing Uty, Ddx3y and Usp9y. We reveal phenotypes absent in single KOs, uncovering a detrimental cumulative effect of Y-gene loss on spermatogenesis.
lab-turner.bsky.social
The transcription activator Zfy2 promotes meiotic pairing and reciprocal recombination between the sex chromosomes.
lab-turner.bsky.social
We found that the histone demethylase Uty functions early in spermatogenesis, regulating the establishment of the spermatogonial stem cell pool and the later spermatogonial differentiation.
lab-turner.bsky.social
While some Y genes are dispensable, others are key for mouse spermatogenesis. We find novel functions for Y genes in spermatogonial, meiotic, post-meiotic and somatic cells.