Toliclab Profile Banner
Iva Tolić Profile
Iva Tolić

@Toliclab

Followers
3K
Following
8K
Media
426
Statuses
1K

Moved to https://t.co/qqX1gi2P81! Biophysics of Mitosis @institutrb, @EMBO member; Ex Group Leader @mpicbg, PD @UNI_FIRENZE, @uni_copenhagen, PhD @PMFZAGREB

Zagreb, Croatia
Joined June 2018
Don't wanna be here? Send us removal request.
@Toliclab
Iva Tolić
6 years
We got an ERC SYNERGY grant #ERCSyG!! With @nenad_pavin @AngelikaAmon and Geert Kops. Huge thanks to our Synergy team, my lab, and ERC! Cannot wait to start this super exciting project! #EUfunded
8
15
158
@Toliclab
Iva Tolić
3 days
National ERC Information Day in Zagreb! Together with other ERC panel members, we shared what happens behind closed panel doors, and with fellow ERC Synergy grantees, I talked about the full journey from the first idea to a funded grant. @ERC_Research https://t.co/ISgy7JGDmw
0
0
10
@BPoD_s
Biomedical Picture of the Day BPoD
4 days
Reappraisal of motor protein CENPE's role in bringing chromosomes together in preparation for accurate cell division 📷 Kruno Vukušić & @Toliclab @institutrb in @NatureComms ➡️ https://t.co/pFHAz7ZrN5 with @DrJohnAnkers
0
5
10
@Toliclab
Iva Tolić
7 days
Researchers in Croatia, join us tomorrow at 9:30 in Zagreb or online to explore ERC grants! I’ll be sharing my experience from both sides of the table - as an ERC panel member and a grantee (Consolidator + Synergy). Bring your questions! @ERC_Research https://t.co/ISgy7JG5wY
0
1
7
@ERC_Research
European Research Council (ERC)
7 days
Researchers in Croatia: join us tomorrow at 9:30 CET to explore ERC grant opportunities! Tune in to get practical guidance, discover how to get support and hear from successful ERC grantees: https://t.co/gD9DbgjQjw
0
7
16
@ERC_Research
European Research Council (ERC)
11 days
Are you a researcher based in Croatia? Interested to apply for ERC funding? Tune in on 10 December to get practical guidance, discover how to get support and hear from successful ERC grantees: https://t.co/gD9DbgjQjw
0
4
14
@Toliclab
Iva Tolić
9 days
Scientists, journalists, communicators, and policymakers in one room, rethinking how we talk about basic research in Europe! With @MarcinMonko, @institutrb, @EK_Hrvatska. https://t.co/WSwE88NqY1 See you at ZG SciComm 2026!
0
0
4
@Toliclab
Iva Tolić
15 days
Do people outside academia understand the potential of EU basic research? I’ll be speaking in Session 2 “Let’s Pop The Balloon” at Zagreb Science Communication Forum 2025, on stepping outside the research bubble and reaching wider publics. @institutrb @EK_Hrvatska
0
1
8
@Toliclab
Iva Tolić
21 days
When our institute’s legendary PR team tells our science story 📹👩‍🔬🧬 @institutrb @KrunoVuk https://t.co/vvwo5NZeQx https://t.co/ll26PG4tU0
1
5
11
@Toliclab
Iva Tolić
2 months
On my way to work - flowers for All Saints’ Day.
0
0
6
@Toliclab
Iva Tolić
2 months
Congrats @KrunoVuk on this remarkable work! Thanks @ERC_Research, @hrzz_science, and @SrceHr for support!
0
0
4
@Toliclab
Iva Tolić
2 months
We propose a kinetochore-centrosome feedback mechanism controlling chromosome movement: chromosomes near centrosomes rely on CENP-E because high Aurora A activity boosts Aurora B at kinetochores, restricting end-on attachments. CENP-E counteracts this by downregulating Aurora B.
1
0
3
@Toliclab
Iva Tolić
2 months
Notably, the dependence of polar chromosomes on CENP-E can be bypassed by using constitutively dephosphorylated Hec1, emphasizing the role of Aurora kinase-mediated Hec1 phosphorylation in preventing congression when CENP-E is absent.
1
0
2
@Toliclab
Iva Tolić
2 months
Does Aurora A at spindle poles directly promote Aurora B activity at kinetochores? Yes, our results show that acute inhibition of Aurora A reduces Aurora B activity at polar kinetochores, accompanied by a decrease in the number of polar chromosomes.
1
0
2
@Toliclab
Iva Tolić
2 months
At poles that contain centrioles, high Aurora A kinase enhances Aurora B activity on kinetochores of polar chromosomes, increasing phosphorylation of microtubule-binding proteins and preventing stable microtubule attachments in the absence of CENP-E.
1
0
2
@Toliclab
Iva Tolić
2 months
Centrosomes inhibit the initiation of congression in the absence of CENP-E, and depletion of centrioles allows chromosomes near acentriolar poles to initiate congression independently of CENP-E.
1
0
2
@Toliclab
Iva Tolić
2 months
In our second paper, we asked why only polar chromosomes depend on CENP-E for congression. We inhibited Plk4 to generate spindles where one pole had centrioles and the other did not. Strikingly, the acentriolar pole (on the right in the movie) rarely had polar chromosomes.
1
0
3
@Toliclab
Iva Tolić
2 months
And now… part two of our twin papers on how chromosomes find their place before division! Led by @KrunoVuk at @institutrb, out in @NatureComms! https://t.co/oUwguXWk5f https://t.co/bCnHSvsJmi Missed the thread on the first paper? Catch up here: https://t.co/ifnldFqiao
@Toliclab
Iva Tolić
2 months
Two back-to-back stories on mitosis led by my incredible postdoc @KrunoVuk at @institutrb, in which we challenge the gliding model of CENP-E-driven chromosome congression! Today in @NatureComms https://t.co/oUwguXWRUN https://t.co/bCnHSvthbQ
1
16
99
@Toliclab
Iva Tolić
2 months
In sum, the first paper shows that chromosome congression is coupled to biorientation, with CENP-E linking the two. A thread on the second paper is coming soon! Congrats @KrunoVuk on this amazing work! We appreciate support from @ERC_Research, @hrzz_science, and @SrceHr.
0
0
5
@Toliclab
Iva Tolić
2 months
We propose that congression operates as a negative feedback loop between the activity of Aurora kinases that oppose congression by destabilizing end-on attachments, but also activate CENP-E, which then promotes congression by opposing the activity of Aurora kinases.
1
0
4
@Toliclab
Iva Tolić
2 months
In our model, stabilization of end-on attachments without CENP-E is delayed due to Aurora kinase-mediated phosphorylation of microtubule-binding proteins and expansion of the fibrous corona, which obstructs attachments. CENP-E counters this by reducing phosphorylation.
1
0
5