Global Analysis of Cereal microProteins Suggests Diverse Roles in Crop Development and Environmental Adaptation

Autor: Kaushal Kumar Bhati, Valdeko Kruusvee, Daniel Straub, Anil Kumar Nalini Chandran, Ki-Hong Jung, Stephan Wenkel

Publikováno v: G3: Genes, Genomes, Genetics, Vol 10, Iss 10, Pp 3709-3717 (2020)

MicroProteins are a class of small single-domain proteins that post-translationally regulate larger multidomain proteins from which they evolved or which they relate to. They disrupt the normal function of their targets by forming microProtein-target

Externí odkaz: https://doaj.org/article/e0c0aed1e5c144728eeaddfd797d9453

Stop CRYing! Inhibition of cryptochrome function by small proteins

Autor: Valdeko Kruusvee, Arendse Maria Toft, Blanche Aguida, Margaret Ahmad, Stephan Wenkel

Publikováno v: Kruusvee, V, Toft, A M, Aguida, B, Ahmad, M & Wenkel, S 2022, ' Stop CRYing! Inhibition of cryptochrome function by small proteins ', Biochemical Society Transactions, vol. 50, no. 2, pp. 773-782 . https://doi.org/10.1042/BST20190062

Plants can detect the presence of light using specialised photoreceptor proteins. These photoreceptors measure the intensity of light, but they can also respond to different spectra of light and thus ‘see' different colours. Cryptochromes, which ar

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fff6cf5874786586d57765ec29a3b962
https://doi.org/10.1042/bst20190062

Global Analysis of Cereal microProteins Suggests Diverse Roles in Crop Development and Environmental Adaptation

Autor: Stephan Wenkel, Kaushal Kumar Bhati, Valdeko Kruusvee, Ki-Hong Jung, Daniel Straub, Anil Kumar Nalini Chandran

Publikováno v: G3: Genes, Genomes, Genetics, Vol 10, Iss 10, Pp 3709-3717 (2020)
G3: Genes|Genomes|Genetics
Bhati, K K, Kruusvee, V, Straub, D, Chandran, A K N, Jung, K-H & Wenkel, S 2020, ' Global Analysis of Cereal microProteins Suggests Diverse Roles in Crop Development and Environmental Adaptation ', G3: Genes, Genomes, Genetics (Bethesda), vol. 10, no. 10, pp. 3709-3717 . https://doi.org/10.1534/g3.120.400794

MicroProteins are a class of small single-domain proteins that post-translationally regulate larger multidomain proteins from which they evolved or which they relate to. They disrupt the normal function of their targets by forming microProtein-target

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6718efa967ad4e974b19c44930541be5
http://g3journal.org/lookup/doi/10.1534/g3.120.400794

Structure of SALL4 zinc finger domain reveals link between AT-rich DNA binding and Okihiro syndrome

Autor: James A Watson, Raphaël Pantier, Uma Jayachandran, Kashyap Chhatbar, Beatrice Alexander-Howden, Valdeko Kruusvee, Michal Prendecki, Adrian Bird, Atlanta G Cook

Publikováno v: Watson, J A, Pantier, R, Jayachandran, U, Chhatbar, K, Alexander-Howden, B, Kruusvee, V, Prendecki, M, Bird, A & Cook, A G 2023, ' Structure of SALL4 zinc finger domain reveals link between AT-rich DNA binding and Okihiro syndrome ', Life Science Alliance, vol. 6, no. 3 . https://doi.org/10.26508/lsa.202201588
Watson, J, Pantier, R, Jayachandran, U, Chhatbar, K, Alexander-Howden, B, Kruusvee, V, Prendecki, M, Bird, A P & Cook, A G 2023, ' Structure of SALL4 zinc-finger domain reveals link between AT-rich DNA binding and Okihiro syndrome ', Life Science Alliance, vol. 6, no. 3, e202201588 . https://doi.org/10.26508/lsa.202201588

Spalt-like 4 (SALL4) maintains vertebrate embryonic stem cell identity and is required for the development of multiple organs, including limbs. Mutations in SALL4 are associated with Okihiro syndrome, and SALL4 is also a known target of thalidomide.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3703f5f9b87bf7d47e8aff81701010b5
https://doi.org/10.26508/lsa.202201588

Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders

Autor: Valdeko Kruusvee, Atlanta G. Cook, Matthew J. Lyst, Ceitidh Taylor, Adrian Bird, Žygimantė Tarnauskaitė

Publikováno v: Kruusvee, V, Lyst, M, Taylor, C, Tarnauskaite, Z, Bird, A & Cook, A 2017, ' Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders ', Proceedings of the National Academy of Sciences, vol. 114, no. 16, pp. E3243-E3250 . https://doi.org/10.1073/pnas.1700731114

Rett syndrome (RTT) is an X-linked neurological disorder caused by mutations in the methyl-CpG–binding protein 2 ( MeCP2 ) gene. The majority of RTT missense mutations disrupt the interaction of the MeCP2 with DNA or the nuclear receptor corepresso

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d7e71621fe3920171be2d61f37262d7
https://hdl.handle.net/20.500.11820/ef6fd464-814e-4e5b-ad20-229bc39be2c3