Generation of a biotinylatable Sox2 mouse model to identify Sox2 complexes in vivo

被引:0
|
作者
Kim Schilders
Evelien Eenjes
Gabriëla Edel
Anne Boerema de Munck
Marjon Buscop van Kempen
Jeroen Demmers
René Wijnen
Dick Tibboel
Robbert J. Rottier
机构
[1] Erasmus Medical Center-Sophia Children’s Hospital,Department of Pediatric Surgery
[2] Netherlands Proteomics Center,Department of Cell Biology
[3] Erasmus Medical Center,undefined
[4] Erasmus Medical Center,undefined
来源
Transgenic Research | 2018年 / 27卷
关键词
Biotinylatable tag; Sox2; Knock-in; In vivo protein complexes;
D O I
暂无
中图分类号
学科分类号
摘要
Sox2 is a Sry-box containing family member of related transcription factors sharing homology in their DNA binding domain. Sox2 is important during different stages of development, and previously we showed that Sox2 plays an important role in branching morphogenesis and epithelial cell differentiation in lung development. The transcriptional activity of Sox2 depends on its interaction with other proteins, leading to ‘complex-specific’ DNA binding and transcriptional regulation. In this study, we generated a mouse model containing a biotinylatable-tag targeted at the translational start site of the endogenous Sox2 gene (bioSox2). This tag was biotinylated by the bacterial birA protein and the resulting bioSox2 protein was used to identify associating partners of Sox2 at different phases of lung development in vivo (the Sox2 interactome). Homozygous bioSox2 mice are viable and fertile irrespective of the biotinylation of the bio tag, indicating that the bioSox2 gene is normally expressed and the protein is functional in all tissues. This suggests that partners of Sox2 are most likely able to associate with the bioSox2 protein. BioSox2 complexes were isolated with high affinity using streptavidin beads and analysed by MALDI-ToF mass spectrometry analysis. Several of the identified binding partners are already shown to have a respiratory phenotype. Two of these partners, Wdr5 and Tcf3, were validated to confirm their association in Sox2 complexes. This bioSox2 mouse model will be a valuable tool for isolating in vivo Sox2 complexes from different tissues.
引用
收藏
页码:75 / 85
页数:10
相关论文
共 50 条
  • [21] Mutations in SOX2 cause anophthalmia
    Judy Fantes
    Nicola K. Ragge
    Sally-Ann Lynch
    Niolette I. McGill
    J. Richard O. Collin
    Patricia N. Howard-Peebles
    Caroline Hayward
    Anthony J. Vivian
    Kathy Williamson
    Veronica van Heyningen
    David R. FitzPatrick
    Nature Genetics, 2003, 33 : 462 - 463
  • [22] Uncovering the Role of Sox2 in Oligodendroglia
    Kuhbandner, Kristina
    JOURNAL OF NEUROSCIENCE, 2018, 38 (19): : 4460 - 4461
  • [23] Sox2: Masterminding the Root of Cancer
    Tam, Wai Leong
    Ng, Huck Hui
    CANCER CELL, 2014, 26 (01) : 3 - 5
  • [24] Sox2 in osteoblast development and craniosynostosis
    Holmes, G.
    Mansukhani, A.
    Ambrosetti, D.
    Cornivelli, L.
    Basilico, C.
    MECHANISMS OF DEVELOPMENT, 2005, 122 : S70 - S70
  • [25] Specificity and application of SOX2 antibody
    Wei, Longqin
    Wang, Lixia
    Pan, Jianhong
    Liu, Lingkang
    Wang, Pengxia
    Wei, Jinyu
    Xu, Xiaoming
    Xing, Qingbo
    Liu, Ping
    Wu, Wende
    Li, Gonghe
    Zheng, Xibang
    POULTRY SCIENCE, 2020, 99 (05) : 2385 - 2394
  • [26] The Role of SOX2 in Hypogonadotropic Hypogonadism
    Tziaferi, V.
    Kelberman, D.
    Dattani, M. T.
    SEXUAL DEVELOPMENT, 2008, 2 (4-5) : 194 - 199
  • [27] Expression pattern of Sox2 during mouse tooth development
    Zhang, Li
    Yuan, Guohua
    Liu, Huan
    Lin, Heng
    Wan, Chunyan
    Chen, Zhi
    GENE EXPRESSION PATTERNS, 2012, 12 (7-8) : 273 - 281
  • [28] Sox2 as a prosensory and proneural gene in the developing mouse cochlea
    Puligilla, Chandrakala
    Dabdoub, A.
    Cheah, K. S.
    Pevny, L. H.
    Kelley, M. W.
    DEVELOPMENTAL BIOLOGY, 2008, 319 (02) : 535 - 535
  • [29] Sox2 as a servant of two masters
    Arun K Mankan
    Veit Hornung
    Nature Immunology, 2015, 16 : 335 - 336
  • [30] SOX2 Expression in Canine Neoplasia
    Miranda, Ileana C.
    Miller, Andrew D.
    VETERINARY PATHOLOGY, 2021, 58 (05) : 964 - 970