. #Botany2025 My institution (JIC in Norwich, UK) is hiring for a tenure-track Group Leader in Discovery Plant Sciences - see more here:
www.jic.ac.uk/vacancies/gr...
Let me know if you have questions!
@hannahraethomas.bsky.social
Young professor at Zhejiang University; PhD from Cornell, Post-doc at the John Innes Centre; interested in plant intercellular communication and grafting π±, science outreach π¬, science policy π€, #Spoonie
. #Botany2025 My institution (JIC in Norwich, UK) is hiring for a tenure-track Group Leader in Discovery Plant Sciences - see more here:
www.jic.ac.uk/vacancies/gr...
Let me know if you have questions!
Pleased to have finally got this method to work in wheat! Find out how you can identify direct targets of transcription factors in wheat using protoplasts and the TARGET method:
dx.doi.org/10.17504/pro...
A very useful method for our group to use! borrilllab.com
#plantbio2025
Amazing talks this morning!
Me too! π
07.05.2025 14:01 β π 1 π 0 π¬ 0 π 0We focus on the integration of #light, #temperature, and #auxin during herbaceous grafting. This review highlights recent advancements and spotlights gaps in our understanding! Please enjoy!
07.05.2025 11:17 β π 0 π 0 π¬ 0 π 0Interested in how abiotic factors regulate plant #grafting? Check out our new review in Planta!
link.springer.com/article/10.1...
Front cover of a postcard to promote an upcoming special issue of the Journal of Experimental Botany titled "Plasmodesmata". The issue will be edited by Tessa Burch-Smith and Jacob Brunkard. The images show the following. Above: silencing signals move out from veins through plasmodesmata in a Nicotiana benthamiana leaf (Jacob Brunkard); Centre: fluorescent Protein moves from a central transformed cell to neighbors through plasmodesmata (Jacob Brunkard); Far right: electronic microscopy reveals nanoscopic structure of plasmodesmata, shown in gray (top) or blue (bottom) (Tessa Burch-Smith; Tina Schreier).
** UPCOMING SPECIAL ISSUE **
Plasmodesmata
Editors: Tessa Burch-Smith & Jake Brunkard
Deadline: 1st Feb 2025
Manuscripts of any format welcomed, please contact the JXB office (bit.ly/JXBissues)
#JXBspecialissues π± π πΏ π§ͺ #plantscience
@pdchristine.bsky.social @tinaschreier.bsky.social
(1/2)
At least the colors are festive? π«£
02.01.2025 13:58 β π 3 π 0 π¬ 0 π 0I'm planning to attend #PlantBio2025 with a few first time US visitors. What #Milwaukee -based or nearby sites would you prioritize for a few days of fun?
02.01.2025 02:51 β π 1 π 0 π¬ 1 π 0Ok people. Iβm drawing silhouettes this afternoon. If you have a paper coming up and you are in need of a #silhouette please let me know and I will have it ready today. As always I upload all my silhouettes to phylopic.org
I also have tutorials on how to put a silhouette in a plot in R.
I'm so excited about my new #orchid. What are some tips to make sure I don't kill it?
18.12.2024 01:47 β π 22 π 1 π¬ 1 π 0Title slide: Will your code run again? Tips for making code reproducible in R
If you missed my talk but still want to learn how to make your R code more reproducible, my slides are here π:
daxkellie.quarto.pub/will-your-co...
All the links to packages and resources I mentioned are there, so hopefully this can be a nice reference, too!
#ESAus2024 #rstats #quartopub π§ͺπ
Devito meme where he's shooting and saying "So anyway I started Blasting". Image modified to haver the Altmetric badge in front of Devito's head, and the caption now reads "So anyway I started Tracking Bluesky". The date is given as the 3rd December 2024
Amye Kenall, VP Product, Data & Analytics Hub, Digital Science, said: βBluesky has become a favored social media channel for research communications professionals and academics. Indeed, in our own research we found over 22% of researchers were using Bluesky over any other social media channel."
03.12.2024 14:00 β π 248 π 51 π¬ 3 π 12Single photon imaging of three capsicum leaves. Leaf 1 is a control. Leaf 2 and 3 are harboring a bioluminescent bacteria growing under different conditions.
When the first experiments in the lab worked! And... the data was significant. πππ#newPI
02.12.2024 12:53 β π 3 π 0 π¬ 0 π 0I mean... he kind of gassed you up. π I'm impressed with your superpower. π
02.12.2024 06:00 β π 3 π 0 π¬ 1 π 0Happy Friday everyone! Here are some cool Arabidopsis mini treesπ΄
Arabidopsis arenosa hypocotyls can undergo extensive secondary growth and the rosettes that develop on top make them look like palm trees π€―I wonder if this can be engineered in thaliana..
π€©π€©π€© I want to see a cross section so bad!
30.11.2024 06:58 β π 0 π 0 π¬ 0 π 0Spending time here on the blue place has been so nice lately. π₯Ή
28.11.2024 14:13 β π 2 π 0 π¬ 0 π 0Yes, this is likely what we will need to do.
26.11.2024 03:35 β π 1 π 0 π¬ 0 π 0It's about 150 bp downstream in the first exon.
25.11.2024 23:33 β π 1 π 0 π¬ 1 π 0I'll definitely look into it! π
25.11.2024 16:20 β π 1 π 0 π¬ 0 π 0Yes we check protein levels in OEπ. We'll check for any off targets in the crispr. What a mess! Hahahaha
25.11.2024 14:44 β π 0 π 0 π¬ 1 π 0Would cosuppresion be consistent in all tissue types? Or do you think it could vary?
25.11.2024 14:41 β π 0 π 0 π¬ 1 π 0Yes, we get a frame shift but transcripts map to the entire gene (besides the deletion site). OE is about 10x higher than WT. Maybe being suppressed? Occams razor would make me think it isn't 2 strange things going on, but who knows!
25.11.2024 14:35 β π 1 π 0 π¬ 1 π 0Seems possible! Then the antibody would still bind!
25.11.2024 14:33 β π 0 π 0 π¬ 1 π 0Deletion is in the middle of the first (or three) exons. Phenotype is fruit ripening timing.
25.11.2024 14:26 β π 0 π 0 π¬ 1 π 0I suppose it's always a possibility. Seems like there would have to have been several mix ups. π¬
25.11.2024 14:25 β π 1 π 0 π¬ 1 π 0It could be a possibility! Phenotype is fruit related. I'll double check that all the experiments were in fruit and not leaf! Would anything explain the protein situation. π€π€
25.11.2024 14:22 β π 1 π 0 π¬ 1 π 0Im totally baffled and hoping the collective mind might have some ideas! π
25.11.2024 13:23 β π 1 π 0 π¬ 0 π 0We have a crispr line w/ 5bp del and phenotype. We can see the edit in gDNA seq, but reads mapped + RT-PCR levels are normal, and the protein can be detected at (we think) full protein mass.
In the OE, reads are higher but phenotype look like crispr pheno?
What could be going on. Any thoughts? π€‘