Shinichi Nakagawa
@smoltblue.bsky.social
78 followers 12 following 10 posts
noncoding RNA Developmental Biology Molecular Biology Hokkaido University
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smoltblue.bsky.social
50 days free access link to the retrotransposon/evolution review!
authors.elsevier.com/a/1keCScQbJF...
authors.elsevier.com
smoltblue.bsky.social
Our new review on retrotransposons is out! I contributed to the “antidote theory” for extremely abundant retrotransposons: their massive expansion must be accompanied by the emergence of an “antidote” system to neutralize the toxic effects of insertion events.
www.cell.com/trends/genet...
Transposon–host arms race: a saga of genome evolution
Once considered ‘junk DNA,’ transposons or transposable elements (TEs) are now recognized as key drivers of genome evolution, contributing to genetic diversity, gene regulation, and species diversific...
www.cell.com
smoltblue.bsky.social
I hadn’t anticipated that a ‘novel’ gene could be identified using such a straightforward approach. Remarkable dedication and devotion.
ryuniwa.bsky.social
I am thrilled that our paper, which is packed with our 10 years of data on the venom proteins of the parasitoid wasp Asobara japonica, has just been published!

Parasitoid wasp venoms degrade Drosophila imaginal discs for successful parasitism | Science Advances www.science.org/doi/10.1126/...
Parasitoid wasp venoms degrade Drosophila imaginal discs for successful parasitism
Two parasitoid wasp venom proteins induce imaginal disc degradation of its host fly Drosophila larva, ensuring parasitism success.
www.science.org
smoltblue.bsky.social
Snow festival at Sapporo.
smoltblue.bsky.social
Thanks to the main organizer, Narry Kim, we are excited to host the first on-site “ASIA RNA Network” meeting (formerly ASIA RNA Club) at Seoul National University from November 3-5, 2025. Save the date!
Reposted by Shinichi Nakagawa
johntngo.bsky.social
We designed MS2 and PP7 binding coat proteins that are degraded in cells except when bound by their hairpin RNAs.

You can check out our pre-print here: tinyurl.com/27p7hyt9,
and listen to a Google AI-generated podcast on it here: notebooklm.google.com/notebook/d71...
Reposted by Shinichi Nakagawa
mendell-lab.bsky.social
I’m thrilled to share a collaborative story from @Mendell_lab and Jan Erzberger labs, led by postdoc extraordinaire Xiaoqiang Zhu. We showed that in addition to their canonical decoding function, tRNAs play a key role in regulating mRNA stability during translation!
www.science.org/doi/10.1126/...
Specific tRNAs promote mRNA decay by recruiting the CCR4-NOT complex to translating ribosomes
The CCR4-NOT complex is a major regulator of eukaryotic messenger RNA (mRNA) stability. Slow decoding during translation promotes association of CCR4-NOT with ribosomes, accelerating mRNA degradation....
www.science.org
Reposted by Shinichi Nakagawa
susanmgasser.bsky.social
Two back-to-back papers in Nature comms from mylab explore the link between destabilization of the actin cytoskeleton and aberrant base excision repair - passing through nuclear actin and the actin-dependent nucleosome remodeler INO80C.
smoltblue.bsky.social
This will yields 2x mix for 800< reactions.

2 µL 2x mix
2 µL DNA mix
37ºC 5 min, 65ºC 5 min

the solution is now ready for transformation. 2x mix solution is stable (-20ºC) at least 3 years in my lab!
smoltblue.bsky.social
I am too lazy to prepare the buffer myself, and here is a slightly mofied version.

A) 2x mix:
NEB buffer 4: 160 µL
Glycerol: 1 mL
NEB 10xBSA (10 mg/mL): 840 µL

B) dilute Exo III (NEB M0265S) 1 in 100 with A

Mix 1600 uL of A, 2 µL of B, and 50 µL ExoT (NEB 2170A)