Tiffany Taylor
@taylorlabgroup.bsky.social
2K followers 1.1K following 96 posts
Professor of Microbial Ecology and Evolution at the Life Sciences Department at the University of Bath. Royal Society Dorothy Hodgkin Research Fellow. Children's author evolution/genetics. Mum. https://tiffanybtaylor.wordpress.com/
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taylorlabgroup.bsky.social
Happy #DNAday 🧬! To celebrate, why not share a bedtime story with a #FutureGeneticist? Listen to my book, Little Letters, illustrated by uber talented James Munro & read by the forever charming children's author AF Harrold
youtu.be/yv3Z8CZ3t_Q
#DNA #GeneticsForKids #ScienceBooks
Little Letters: an introduction to genetics
written by Tiffany Taylor, illustrated by James Munro, read by A. F. Harrold.Join Berry, Daisy and Spike, as an extraordinary close encounter turns a family ...
youtu.be
Reposted by Tiffany Taylor
Reposted by Tiffany Taylor
epcrocha.bsky.social
Willing to join us @pasteur.fr for a PhD for a project on how interactions between mobile genetic elements shape bacterial adaptation? Subject to be tailored to candidates with keen interest in evolution, genomics, computational biology, microbiology. Check www.pasteur.fr/en/education...
taylorlabgroup.bsky.social
Excited to share brilliant work @josie-e.bsky.social. She built a minimal type I-F CRISPR-Cas system where parts (like spacers) can be easily swapped. Against a panel of phages it gave full protection in most cases—though for some, immunity was stronger in low-nutrient growth. Check out her 🧵 below!
Reposted by Tiffany Taylor
Reposted by Tiffany Taylor
cellmorphosero.bsky.social
What are your "good hands" training tips? @baym.lol and others?
- Slow down
- Pay attention
- Visualise doing the whole protocol. What do you need to have labelled when? Where are you standing? What are you doing during the incubation? Etc.
- Start new methods with 2-3 small low-stakes experiments.
baym.lol
Every few months the "good lab hands" thing comes up and it misses a key point: you can learn to have good hands. Training matters.

Good hands aren't some magic gift from the PCR gods, you have to develop them through directed repetitive practice, like any other skill
Reposted by Tiffany Taylor
vscooper.micropopbio.org
What shapes the moment when you say, this is who I want to be?

Could one classroom research experience be that catalyst?
Could a summer camp for teachers help them make students become scientists? 🧪🧫🧬🔬

YES. This is EvolvingSTEM. So proud of this team.
youtu.be/sv3tcwRs2PE?...
EvolvingSTEM Summer of Transformation 2025
YouTube video by Evolving STEM
youtu.be
taylorlabgroup.bsky.social
Dammit. Edit to first post, T > G.
taylorlabgroup.bsky.social
A big thank you to my co-authors: Joshua Cherry, @gretelwaugh.bsky.social Also thank you to @peteralind.bsky.social for his helpful feedback on the manuscript and for pointing out that GnT motifs bias experimental evolution surprisingly often!
taylorlabgroup.bsky.social
Finally, the GnT motif mutation rates determined for Pseudomonas closely match those determined for Salmonella, so we're confident that our calculated rates for GnT motifs can be used to both find and quantify T:A→G:C mutation hotspots in many other species of bacteria. (8/8)
taylorlabgroup.bsky.social
GnT motifs are very short (≥8bp depending on G tract length), which means these hotspots are very common elements in bacterial genomes! For example, Pseudomonas fluorescens has hotspot GnT motifs that can cause a non-synonymous mutation in ~20% of reading frames. (7/8)
taylorlabgroup.bsky.social
We also demonstrated that GnT motifs can be used to increase the rate and predictability of evolution. If you synonymously convert the neighbouring nucleotides around adaptive T:A positions into GnT motifs, adaptive evolution can happen significantly faster. (6/8)
taylorlabgroup.bsky.social
For example, if a G4T sequence (i.e. GGGGT) is flanked by a 5’ AC and a 3’ A, there’s almost no hotspot (the T:A→G:C mutation rate is ~5-fold higher than baseline). But if a G4T sequence is flanked by a 5’ GA and 3’ C, the T:A→G:C rate is ∼1100-fold higher than baseline. (5/8)
taylorlabgroup.bsky.social
We created T:A→G:C mutational hotspots by synonymously altering: (a) the length of the GnT sequence, (b) the dinucleotide 5’ to the homopolymer G tract, and (c) the nucleotide 3’ to the T. Together, the flanking nucleotides change the mutation rate by orders of magnitude. (4/8)
taylorlabgroup.bsky.social
In this work, we create mutational hotspots in the Pseudomonas fluorescens genome using synonymous nucleotide changes to alter the GnT sequence and its neighbours. We show that GnT hotspots are determined by a GnT sequence and the nucleotides immediately flanking it. (3/8)
taylorlabgroup.bsky.social
In a recent paper analysing Salmonella and others, Cherry 2023 found that homopolymeric tracts of G (≥3) with a 3’ T frequently mutate so that the T is substituted with another G: I.e. GGGT→GGGG. This rate increases the longer the G tract (GnT). academic.oup.com/gbe/article/... (2/8)
T Residues Preceded by Runs of G Are Hotspots of T→G Mutation in Bacteria
Abstract. The rate of mutation varies among positions in a genome. Local sequence context can affect the rate and has different effects on different types
academic.oup.com
taylorlabgroup.bsky.social
🦠 New paper led by James Horton (feat. J Cherry & @gretelwaugh.bsky.social) reveals GnT DNA motif can boost T→A mutation rates up to 1000×, & how tweaking nearby bases can fine-tune its potency.
General across bacteria + potential in synbio.
📄 academic.oup.com/mbe/advance-ar…
🔗 James’s thread ⬇️
https://academic.oup.com/mbe/advance-ar…