Literature DB >> 23419774

The CATS (FAM64A) protein is a substrate of the Kinase Interacting Stathmin (KIS).

Leticia Fröhlich Archangelo1, Philipp A Greif, Alexandre Maucuer, Valérie Manceau, Naresh Koneru, Carolina L Bigarella, Fernanda Niemann, Marcos Tadeu dos Santos, Jörg Kobarg, Stefan K Bohlander, Sara Teresinha Olalla Saad.   

Abstract

The CATS protein (also known as FAM64A and RCS1) was first identified as a novel CALM (PICALM) interactor that influences the subcellular localization of the leukemogenic fusion protein CALM/AF10. CATS is highly expressed in cancer cell lines in a cell cycle dependent manner and is induced by mitogens. CATS is considered a marker for proliferation, known to control the metaphase-to-anaphase transition during the cell division. Using CATS as a bait in a yeast two-hybrid screen we identified the Kinase Interacting Stathmin (KIS or UHMK1) protein as a CATS interacting partner. The interaction between CATS and KIS was confirmed by GST pull-down, co-immunoprecipitation and co-localization experiments. Using kinase assay we showed that CATS is a substrate of KIS and mapped the phosphorylation site to CATS serine 131 (S131). Protein expression analysis revealed that KIS levels changed in a cell cycle-dependent manner and in the opposite direction to CATS levels. In a reporter gene assay KIS was able to enhance the transcriptional repressor activity of CATS, independent of CATS phophorylation at S131. Moreover, we showed that CATS and KIS antagonize the transactivation capacity of CALM/AF10.In summary, our results show that CATS interacts with and is a substrate for KIS, suggesting that KIS regulates CATS function.
Copyright © 2013 Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23419774     DOI: 10.1016/j.bbamcr.2013.02.004

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  8 in total

1.  The myristoylated alanine-rich C kinase substrate differentially regulates kinase interacting with stathmin in vascular smooth muscle and endothelial cells and potentiates intimal hyperplasia formation.

Authors:  Dan Yu; Ramkishore Gernapudi; Charles Drucker; Rajabrata Sarkar; Areck Ucuzian; Thomas S Monahan
Journal:  J Vasc Surg       Date:  2019-03-28       Impact factor: 4.268

2.  FAM64A positively regulates STAT3 activity to promote Th17 differentiation and colitis-associated carcinogenesis.

Authors:  Zhi-Sheng Xu; Hong-Xia Zhang; Wei-Wei Li; Yong Ran; Tian-Tian Liu; Mei-Guang Xiong; Qing-Lan Li; Su-Yun Wang; Min Wu; Hong-Bing Shu; Huimin Xia; Yan-Yi Wang
Journal:  Proc Natl Acad Sci U S A       Date:  2019-05-06       Impact factor: 11.205

3.  Postnatal expression of cell cycle promoter Fam64a causes heart dysfunction by inhibiting cardiomyocyte differentiation through repression of Klf15.

Authors:  Ken Hashimoto; Aya Kodama; Momoko Ohira; Misaki Kimoto; Reiko Nakagawa; Yuu Usui; Yoshihiro Ujihara; Akira Hanashima; Satoshi Mohri
Journal:  iScience       Date:  2022-04-30

4.  CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells.

Authors:  Isabella Barbutti; Juliana M Xavier-Ferrucio; João Agostinho Machado-Neto; Lauremilia Ricon; Fabiola Traina; Stefan K Bohlander; Sara Teresinha Olalla Saad; Leticia Fröhlich Archangelo
Journal:  Oncotarget       Date:  2016-10-18

5.  Aberrant FAM64A mRNA expression is an independent predictor of poor survival in pancreatic cancer.

Authors:  Yan Jiao; Zhuo Fu; Yanqing Li; Wei Zhang; Yahui Liu
Journal:  PLoS One       Date:  2019-01-29       Impact factor: 3.240

6.  PIMREG, a Marker of Proliferation, Facilitates Aggressive Development of Cholangiocarcinoma Cells Partly Through Regulating Cell Cycle-Related Markers.

Authors:  Zhao-Ming Jiang; Hong-Bin Li; Shu-Guo Chen
Journal:  Technol Cancer Res Treat       Date:  2020 Jan-Dec

7.  FAM64A is an androgen receptor-regulated feedback tumor promoter in prostate cancer.

Authors:  Yingchen Zhou; Longhua Ou; Jinming Xu; Haichao Yuan; Junhua Luo; Bentao Shi; Xianxin Li; Shangqi Yang; Yan Wang
Journal:  Cell Death Dis       Date:  2021-07-02       Impact factor: 8.469

8.  Human Ovarian Granulosa Cells Isolated during an IVF Procedure Exhibit Differential Expression of Genes Regulating Cell Division and Mitotic Spindle Formation.

Authors:  Maciej Brązert; Wiesława Kranc; Błażej Chermuła; Katarzyna Kowalska; Maurycy Jankowski; Piotr Celichowski; Michal Jeseta; Hanna Piotrowska-Kempisty; Leszek Pawelczyk; Maciej Zabel; Paul Mozdziak; Bartosz Kempisty
Journal:  J Clin Med       Date:  2019-11-20       Impact factor: 4.241

  8 in total

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