Kaia Mattioli
@kaiamattioli.bsky.social
570 followers 290 following 180 posts
K99/R00 postdoc, 24/7 feminist @ Harvard/BWH // generally fascinated by genomes // big fan of reality tv, good writing, crosswords, and cats // obsessed with my e-bike // she/her
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kaiamattioli.bsky.social
our work on the molecular differences between transcription factor isoforms is out now in Molecular Cell!

key point: 2/3rds of TF isos differ in properties like DNA binding & transcriptional activity

many are "negative regulators" & misexpressed in cancer

www.sciencedirect.com/science/arti...
kaiamattioli.bsky.social
ever since i was a little girl i have wanted to spend all day changing the length of my research proposals to be in compliance with different arbitrary page number requirements
kaiamattioli.bsky.social
yes true, but they can't really do that if they're hired to be fully dry... (seeing a lot of solely computational posts)
kaiamattioli.bsky.social
tepid take: a lotttttt of job postings for bio-AI researchers, not enough job postings for generating-the-extremely-necessary-data-for-bio-AI researchers
Reposted by Kaia Mattioli
jbyoder.org
Really cool, conceptually simple approach here: cross-referencing grant proposal scores with literature citations and explicit acknowledgments in drug patents to identify patents linked to projects that wouldn't have been funded given a smaller budget
Reposted by Kaia Mattioli
jengreitz.bsky.social
Excited for a major milestone in our efforts to map enhancers and interpret variants in the human genome:

The E2G Portal! e2g.stanford.edu

This collates our predictions of enhancer-gene regulatory interactions across >1,600 cell types and tissues.

Uses cases 👇

1/
Reposted by Kaia Mattioli
genometdcc.org
New video! Discover how transcription factors find their way through tightly packed DNA. 🧪🧬💻👩‍🔬

www.youtube.com/watch?v=gOta...

Luca Mariani & Martha Bulyk introduce PIONEAR-seq, revealing how DNA flexibility shapes gene regulation.

Recently published in @natsmb.nature.com
DNA Bendability Regulates Transcription Factor Binding to Nucleosomes (PIONEAR-seq)
YouTube video by GenomeTDCC
www.youtube.com
kaiamattioli.bsky.social
my twitter algorithm is completely overrun with the AI for bio hype machine and I would like to see other things sometimes
kaiamattioli.bsky.social
are there any gene regulation/genomics paper/preprint-aggregating accounts on here I should be following?
kaiamattioli.bsky.social
editorial manager: your manuscript status is none of your business, actually
kaiamattioli.bsky.social
happy postdoc appreciation week to all who celebrate <3
kaiamattioli.bsky.social
what postdocs actually want:
- to not have their grants canceled
- reasonable chances at getting an academic position
- job security
- a thriving private sector so the entire research system can flourish <3

higher ed institutions in 2025:
- best i can do is an origami night
kaiamattioli.bsky.social
Decades of progress in science, engineering, & medicine will allow me to live a long & meaningful life, but there's still so much to do. I'm proud to be contributing to progress. And for my family's sake, I hope our country continues to publicly fund life-saving research. /end
kaiamattioli.bsky.social
I’m dreaming up future directions that leverage my expertise in genomics to study how aberrant splicing affects GRNs in breast, ovarian, and other solid tumors. I’ll be on the job market soon 🤓; if you’re interested in this type of work (& hiring...), please reach out!
kaiamattioli.bsky.social
I love thinking about gene regulation & RNA processing, & I’m newly motivated to study how these fundamental processes go wrong in cancer. Alternative isoforms add a layer of complexity that we must understand more deeply in order to effectively detect & treat cancer.
kaiamattioli.bsky.social
Eerily/serendipitously, before all this, I was awarded a K99 to study the role of alternative isoforms in breast cancer. Our prev work found hundreds of TF isoforms that are molecularly distinct & associated with cancer -- are they contributing to tumorigenic phenotypes in cells?
kaiamattioli.bsky.social
I’m so thankful to be a patient at MGH Cancer Center, seen by physician-scientists who have been studying this for decades. And I’m thankful for the BioBank for reaching out to me & giving me an opportunity to control what I can.
kaiamattioli.bsky.social
But now that I’ve been sitting with this for a while, those initial emotions (which are v much still present in my brain) have been joined by gratitude & determination. I’m so thankful we sequenced the human genome! I’m so thankful for PARP inhibitors! I’m so thankful for science
kaiamattioli.bsky.social
Then I got diagnosed, & I suddenly found myself consumed by worry, wishing I didn’t know The Statistics. I'd already been dealing with an onset of an autoimmune condition postpartum & parenting a toddler, all while trying to be a productive postdoc. It was (& still is) too much.
kaiamattioli.bsky.social
Since finding out, I’ve been scared, sad, angry... I almost wished I didn’t know. It’s kind of crazy: if you had asked me before diagnosis if I would want to know, I would have 100% said absolutely of course, this is what genetics is for, slot me into those screenings baby!
kaiamattioli.bsky.social
Of course, breast cancer is the poster child for early detection; the situation is much grimmer for ovarian cancer, which has no effective screening yet. The recommendation is to get a prophylactic oophorectomy (removal of the ovaries) around the age of 45.
kaiamattioli.bsky.social
As the pic above shows, I’ve been slotted immediately into high risk screening. I’ll get yearly mammograms & breast MRIs. I just completed my first round & everything was clear, to my huge relief. I may opt for a mastectomy at some point, but I’m not ready to make that call yet.
kaiamattioli.bsky.social
(Side note: there’s a longer version of this story that involves a missed opportunity for me to have detected this variant myself when I had my whole genome sequenced in 2017 because I failed to analyze the **indel** vcf file…....... and 23&Me false negatives...)
kaiamattioli.bsky.social
Follow up tests showed a single nucleotide insertion in exon 11 of BRCA2. A frameshift! Upstream of the DNA-binding domain, even. A textbook pathogenic mutation if I’ve ever seen one.
kaiamattioli.bsky.social
The letter advised me to follow up if I wanted more information. I decided I couldn't NOT know the details, so I reached out to the incredible Molecular Medicine team at
Mass General Brigham for clinical validation. I have a small family, so our health history is a bit sparse.