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Rog lab at the University of Utah

@theroglab.bsky.social
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Cell biology of chromosomes in meiosis 🏳️‍🌈

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Reposted by Rog lab at the University of Utah
American Society for Cell Biology @ascbiology.bsky.social · 19/09/2025
🎉 Congratulations to Needhi Bhalla, UC Santa Cruz (www.bhallalab.com ), named a 2025 #ASCB Fellow! This honor celebrates her outstanding contributions to cell biology, leadership, & service. Fellows will be recognized at #CellBio2025 in Philadelphia this December. #CellBiology
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Reposted by Rog lab at the University of Utah
EMBL DB unit @embldbunit.bsky.social · 27/03/2025
Only a few days left to register to attend virtually the @embl.org symposium on the "Wild Frontier of Model Systems". Don't miss this opportunity if you are interested in exploring unconventional model organisms for a better understanding of biology, ecology and evolution
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Rog lab at the University of Utah @theroglab.bsky.social · 05/03/2025
www.theguardian.com/environment/...
theguardian.com
Canada goose fights off bald eagle in rare, symbolism-laden battle on ice
Photographer captures 20-minute clash between birds emblematic of Canada and US amid high trade tensions
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Reposted by Rog lab at the University of Utah
University of Utah School of Biological Sciences @uofubiology.bsky.social · 27/02/2025
News! @theroglab.bsky.social Gordon et al. discovers synaptonemal complex wets & aligns chromosomes, a crucial step in sexual reproduction, where errors in chromosome# can be fatal to the embryo. @utah.edu Read in Science Advances www.science.org/doi/full/10....
science.org
The synaptonemal complex aligns meiotic chromosomes by wetting
During sexual reproduction, the synaptonemal complex aligns the maternal and paternal chromosomes by wetting.
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Reposted by Rog lab at the University of Utah
Abby Dernburg @adernburg.bsky.social · 21/02/2025
I hope that everyone in the private sector who depends on federal grants to train their researchers and staff, pay for their services and products, or benefits in any other way from federal funding will come out to #standupforscience!
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Reposted by Rog lab at the University of Utah
MAYosis @mayosis.bsky.social · 30/01/2025
Ofer Rog @theroglab.bsky.social from @utah.edu will talk about "Regulating sister interactions during meiosis" on May 21st Learn more about Dr. Rog's work : theroglab.org --> Register here: meiosis.cornell.edu/mayosis2025/...
theroglab.org
The Rog Lab
The Rog Lab, headed by Dr. Ofer Rog, is located at the Department of Biology in the University of Utah at Salt Lake City, and uses C. elegans and yeast to study meiosis, sexual reproduction and chrom...
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Rog lab at the University of Utah @theroglab.bsky.social · 15/01/2025
Much more inside. As usual, hit us up if you have any feedback!
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Rog lab at the University of Utah @theroglab.bsky.social · 15/01/2025
Finally, we used our kinetic information to derive the total number of DSBs. We found an average of 40 DSBs per nucleus in wild-type meiosis suggesting a ratio of 7:1 of DSBs to crossovers, and more DSBs in mutant scenarios.
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Rog lab at the University of Utah @theroglab.bsky.social · 15/01/2025
Second, strand invasion kinetics were similar for repair events templated by the homolog versus the sister. This was surprising, since a leading hypothesis is that DSBs that don't find the homologs stall and are only repaired at the end of meiosis using the sister chromatid.
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Rog lab at the University of Utah @theroglab.bsky.social · 15/01/2025
We made 3 crucial findings. First, we found that most repair events finish the strand-invasion step in 1-2 hours. This is true for both endogenous (SPO-11-induced) and irradiation-induced DSBs.
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Rog lab at the University of Utah @theroglab.bsky.social · 15/01/2025
The inspiration was beautiful work by Sarit and Nicola, who used auxin-mediated degradation of SPO-11 to extinguish new meiotic DSBs. We used a cytological marker - RAD-51 - which marks strand-invasion and quantified the kinetics of their disappearance. pubmed.ncbi.nlm.nih.gov/36170820/
pubmed.ncbi.nlm.nih.gov
Continuous double-strand break induction and their differential processing sustain chiasma formation during Caenorhabditis elegans meiosis - PubMed
Faithful chromosome segregation into gametes depends on Spo11-induced DNA double-strand breaks (DSBs). These yield single-stranded 3' tails upon resection to promote crossovers (COs). While early Mre1...
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Rog lab at the University of Utah @theroglab.bsky.social · 15/01/2025
New preprint from the lab! We defined the kinetics of strand invasion during meiosis in C. elegans. Great work from Antonia, Henry and Divya. www.biorxiv.org/content/10.1...
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Rog lab at the University of Utah @theroglab.bsky.social · 10/11/2024
Looking for a summer undergraduate research opportunity? Come work with us! Apply to SPUR at the University of Utah - it including a stipend and funds for travel and housing: our.utah.edu/research-sch... our.utah.edu/spur/underst... Reach out if you have any questions!
our.utah.edu
Summer Program for Undergraduate Research (SPUR) - Office of Undergraduate Research
SPUR is a nationally competitive opportunity that provides undergraduate students with an intensive 10-week summer research experience under the mentorship of a University of Utah…
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
We’d love to get feedback and suggestions. Kudos to Kewei, an amazing grad student who developed CheC-PLS over the last 5 years; to Chloe and Lexy (now with her own lab, new-car-smell and all, at UMinnesota); and to Lisa and a super-talented undergrad, Kaan.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
So Skp1 has been moonlighting for >100 million years. Which adds a new twist to the SC paradox: how does a highly conserved protein (Skp1) maintains intimate interaction with quickly diverging proteins in a way that does not leave a clear evolutionary mark in their sequence?
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
In both nematode, Skp1 is not only necessary for assembly of the SC onto chromosomes - without dimerization-competent Skp1, SC proteins are absent.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
Lisa turned to the distantly related nematode P. pacificus, and found that the answer is a resounding ‘yes’. Ppa-SKR-1 localize to the middle of the SC, and a conserved dimerization interface in Skp1 is specifically required for SC assembly in Pristi, as it is in elegans.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
Recently, Yumi Kim's lab made an intriguing discovery: Skp1, a conserved subunit of the SCF ubiquitin ligase complex (SKR-1 in C. elegans), moonlights as a structural component of the SC. Lisa decided to test whether this function is conserved. 10.1126/sciadv.adl4876
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
On the other hand, the protein sequence is incredibly divergent between and within clades, so much so that the genes had to be independently cloned in different model organisms. (More on that in Lisa’s previous paper.) elifesciences.org/articles/30823
elifesciences.org
Live cell-lineage tracing and machine learning reveal patterns of organ regeneration
A combination of live cell tracking, cell-lineage tracing and machine learning shows that injured sensory organs repair accurately regardless of the extent of damage.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
#3: Skp1 in the SC. SC proteins have intriguing evolutionary history: they build a highly conserved structure AND (almost) all subunits are co-dependent for assembly.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
That has crucial implications: ZHP-3 can sample the entire 6um chromosome in tens of minutes, whereas SYP-3 cannot. By extension, ZHP-3 is capable of efficiently transducing a crossover signal, whereas SYP-3 would be unlikely to.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
The second important finding came from comparing the diffusion of an SC component (SYP-3) vs a regulator of crossovers (ZHP-3). ZHP-3 diffuses 4-9 times faster than SYP-3 (depending on meiotic stage).
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
(Black-boxing some amazing tech here; check out the preprint for details.) This finding confirmed a crucial aspect of the coarsening hypothesis.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
However, a crucial piece of this model has not been tested: do molecules diffuse within the SC? Lexy directly tested that. By sparsely labeling SC components and crossover regulators, she was able to observe single molecules in live gonads.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
This idea, and beautiful data from worms and plants (from Raphael Mercier, Chris Morgan and others) suggested coarsening regulates genetic exchanges (crossovers).
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
#2: Diffusion within the synaptonemal complex (SC). A few years ago @adernburg.bsky.social and I showed the SC has liquid properties. doi.org/10.7554/eLif...
doi.org
The synaptonemal complex has liquid crystalline properties and spatially regulates meiotic recombination factors
Formation of a phase-separated interface between homologous chromosomes during meiosis enables regulatory signals to spread in cis over long distances, illuminating the longstanding mystery of crossov...
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
And perhaps not less important - potential for many future experiments. Should be noted: nothing in the design confines CheC-PLS to budding yeast, so it should be adaptable to other model organisms.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
Our data revealed sliding of cohesin on DNA (presumably loop extrusion); positioning of nucleosomes; and, AFAIK, the first binding patterns of cohesins in the rDNA locus. Much more data inside.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
We also performed a CheC-PLS on isolated nuclei, using Rec8-GFP and nanobodies targeted to GFP and tethered to a methyltransferase. (This variation is related to recently published techniques like DiMeLo-seq and SAMOSA). cc @astraight.bsky.social
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
We developed CheC-PLS on meiotic chromosomes in budding yeast. We tagged the cohesin subunit Rec8 and recapitulated ChIP & HiC data.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
How do we do that? We mark DNA by tethering a methyltransferase to a protein. (This is similar to DamID.) Next, we sequence genomic DNA using Nanopore. This gives us 1) long reads (some >200kb) 2) directly detecting methylated bases, revealing where the protein ‘touched’ the chr.
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
#1: CheC-PLS (pronounced ‘check, please’) is a new genomic technique. It relates to ChIP, but adds 4 crucial features: 1. contiguity (how distant events are regulated) 2. history (where a protein has been) 3. heterogeneity (single cell data) 4. context (mapping repeats).
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Rog lab at the University of Utah @theroglab.bsky.social · 01/07/2024
Three (3) new pre-prints from the lab! Very proud of this work that spans approaches and model organisms, and highlights the many approaches the lab undertakes. CheC-PLS: doi.org/10.1101/2024... Diffusion in the SC: doi.org/10.1101/2024... Skp1:
doi.org
Decoding chromosome organization using CheC-PLS: chromosome conformation by proximity labeling and long-read sequencing
bioRxiv - the preprint server for biology, operated by Cold Spring Harbor Laboratory, a research and educational institution
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Rog lab at the University of Utah @theroglab.bsky.social · 19/01/2024
So honored to be awarded the Early Career Medal by GSA. And to be in such esteemed company. Couldn't have done it without the truly amazing members of my lab, my mentors and my awesome colleagues at the University of Utah genestogenomes.org/preeminent-g...
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Rog lab at the University of Utah @theroglab.bsky.social · 12/12/2023
Much more analysis inside, but one particularly intriguing finding: many of the the suppressors were in completely conserved positions (a rarity in SC proteins). They perfectly suppressed the original mutation, but didn't exhibit any phenotypes on their own!
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Rog lab at the University of Utah @theroglab.bsky.social · 12/12/2023
The story starts with a saturated suppressor screen for a temperature-sensitive mutation that destabilizes the SC. Lisa identified dozens of suppressors, that all mapped to three short stretches in SC proteins.
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Rog lab at the University of Utah @theroglab.bsky.social · 12/12/2023
First science post from the Rog lab: Proud to have out this paper at PNAS from Lisa and Jesus on the synaptonemal complex in C. elegans. It includes what is probably the most beautiful genetic data I was ever involved in analyzing - check it out! www.pnas.org/doi/10.1073/...
pnas.org
PNAS
Proceedings of the National Academy of Sciences (PNAS), a peer reviewed journal of the National Academy of Sciences (NAS) - an authoritative source of high-impact, original research that broadly spans...
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Reposted by Rog lab at the University of Utah
Stephan Gruber @gruberlab.bsky.social · 04/11/2023
First preprint 📢 on bsky: New work on the Wadjet defence system by @roisnehamelinf.bsky.social & @drhonsworth.bsky.social revealing beautiful & exciting structures of JET on plasmid DNA. With loop extrusion, obstacles, DNA bending, kinking, cleavage 🦠🧫 🧪 t.co/RaO7IO3zDk  With help from @DCI_Lausanne
Structures of JetABCD complex on kinked plasmid DNA.
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Rog lab at the University of Utah @theroglab.bsky.social · 26/10/2023
With the College of Science team at NDiSTEM SACNAS conference in Portland. Booth 642. Come over if you’d like to chat!
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