Always a pole cell never a pgc! Transcription may be essential to segregate healthy and defective pole cells. Pole cells that never activate their zygotic genome and retain what mommy gave them, die. Pole cells that activate their zygotic genome too much also die. Life is a balance! 8/8
Sheri
@sagrill.bsky.social
K99 Postdoctoral fellow in the Lehmann lab at the Whitehead Institute
Lost children are the first germ cells to die during embryogenesis, they fail to undergo trans-epithelial migration and are lost in the gut. When we rescue their death with chk2 mutants they still retain maternal transcripts and do not express zygotic transcripts. 7/8
Finally, our data uncovered a second unexpected cluster of germ cells that we term lost children. These germ cells are isolated from the 9 to 12 hour AEL window as coalesced germ cells. These germ cells completely retain their maternal transcriptome and never activate zygotic gene expression. 6/8
As It turns out, nanos actually inhibits Zelda protein levels in pole cells! Now we find that pole cells in nanos mutants have a dramatic increase in Zelda protein. Nanos -> Zelda -> class II genes. This sheds new light for how nanos protects germline identity and prevents its somatization. 5/8
We found that while these class II genes are expressed in pole cells, their translation is inhibited by nanos. Unexpectedly, when we examined class II transcription in nanos mutants we found a dramatic increase in their transcription!! 4/8
Instead, their transcription is dependent on the pioneer factor #Zelda, where loss of Zelda results in loss of early pole cell transcription. 3/8
This work would not have been possible without the incredible snATAC-seq atlas of the Drosophila embryo from @diegoisworking.bsky.social @jshendure.bsky.social and @eileen-furlong.bsky.social which helped us discover that germ cells retain a totipotent chromatin state throughout development!
So proud of my lab mate @sagrill.bsky.social (whose on the job market 👀) for this magnum opus from @remlehmann.bsky.social lab @whiteheadinstitute.bsky.social ScRNA-seq of 🪰 germ cells reveals new biology, answers age old questions, and proposes new paradigms! 1/8 www.biorxiv.org/content/10.6...
Thank you @arjunarajakumar.bsky.social Couldn't have done it without you!
So proud of my lab mate @sagrill.bsky.social (whose on the job market 👀) for this magnum opus from @remlehmann.bsky.social lab @whiteheadinstitute.bsky.social ScRNA-seq of 🪰 germ cells reveals new biology, answers age old questions, and proposes new paradigms! 1/8 www.biorxiv.org/content/10.6...
Incredibly excited to share my new preprint! 🪰🧬 Ever wondered how germ cells can specify their fate without having a dedicated transcriptional program? We found that germ cells keep the uncommitted chromatin state of the early embryo www.biorxiv.org/content/10.6...
Decoupling Transcription from Cell Fate Preserves Germ Cell Totipotency
Only germ cells can give rise to a totipotent embryo, yet a conserved transcriptional program for germ cell identity remains elusive. Profiling Drosophila primordial germ cells (PGCs) across embryogen...
biorxiv.org