Literature DB >> 36066707

Preparation of Mitotic Cells for Fluorescence Microscopy.

Yuji Tanno1.   

Abstract

Cell cycle-dependent regulation of chromosome is a dynamic event. After replication in S phase, sister chromatids show dynamic behavior including condensation, alignment, and segregation in M phase. These beautiful behaviors of chromosomes observed through the microscope have fascinated people since more than 100 years ago, and now we can sketch the dynamics of regulatory proteins and their posttranscriptional modifications through the fluorescent microscope. The purpose of this chapter is describing the basic methods of immunofluorescence analysis of mitotic cells and chromosomes. Besides, the key ideas for improving the preparation of the specimen are also described. Because the characteristic of the proteins of your interest differs one by one, modifying the method might cause the crucial improvement in the observation.
© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Antibody; Chromatin; Chromosome; Immunofluorescence; Immunostaining; Microscopy; Mitosis

Mesh:

Year:  2023        PMID: 36066707     DOI: 10.1007/978-1-0716-2433-3_4

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  11 in total

1.  Two histone marks establish the inner centromere and chromosome bi-orientation.

Authors:  Yuya Yamagishi; Takashi Honda; Yuji Tanno; Yoshinori Watanabe
Journal:  Science       Date:  2010-10-08       Impact factor: 47.728

2.  Human Bub1 defines the persistent cohesion site along the mitotic chromosome by affecting Shugoshin localization.

Authors:  Tomoya S Kitajima; Silke Hauf; Miho Ohsugi; Tadashi Yamamoto; Yoshinori Watanabe
Journal:  Curr Biol       Date:  2005-02-22       Impact factor: 10.834

3.  Phosphorylation of mammalian Sgo2 by Aurora B recruits PP2A and MCAK to centromeres.

Authors:  Yuji Tanno; Tomoya S Kitajima; Takashi Honda; Yasuto Ando; Kei-Ichiro Ishiguro; Yoshinori Watanabe
Journal:  Genes Dev       Date:  2010-10-01       Impact factor: 11.361

4.  Histone H3 serine 10 phosphorylation by Aurora B causes HP1 dissociation from heterochromatin.

Authors:  Toru Hirota; Jesse J Lipp; Ban-Hock Toh; Jan-Michael Peters
Journal:  Nature       Date:  2005-10-12       Impact factor: 49.962

5.  Regulation of mitotic chromosome cohesion by Haspin and Aurora B.

Authors:  Jun Dai; Beth A Sullivan; Jonathan M G Higgins
Journal:  Dev Cell       Date:  2006-11       Impact factor: 12.270

6.  Shugoshin collaborates with protein phosphatase 2A to protect cohesin.

Authors:  Tomoya S Kitajima; Takeshi Sakuno; Kei-ichiro Ishiguro; Shun-ichiro Iemura; Tohru Natsume; Shigehiro A Kawashima; Yoshinori Watanabe
Journal:  Nature       Date:  2006-03-15       Impact factor: 49.962

7.  Production of large numbers of mitotic mammalian cells by use of the reversible microtubule inhibitor nocodazole. Nocodazole accumulated mitotic cells.

Authors:  G W Zieve; D Turnbull; J M Mullins; J R McIntosh
Journal:  Exp Cell Res       Date:  1980-04       Impact factor: 3.905

Review 8.  Mechanisms of chromosome behaviour during mitosis.

Authors:  Claire E Walczak; Shang Cai; Alexey Khodjakov
Journal:  Nat Rev Mol Cell Biol       Date:  2010-01-13       Impact factor: 94.444

9.  Unattached kinetochores rather than intrakinetochore tension arrest mitosis in taxol-treated cells.

Authors:  Valentin Magidson; Jie He; Jeffrey G Ault; Christopher B O'Connell; Nachen Yang; Irina Tikhonenko; Bruce F McEwen; Haixin Sui; Alexey Khodjakov
Journal:  J Cell Biol       Date:  2016-02-01       Impact factor: 10.539

10.  Aurora B kinase activity is regulated by SET/TAF1 on Sgo2 at the inner centromere.

Authors:  Yuichiro Asai; Koh Fukuchi; Yuji Tanno; Saki Koitabashi-Kiyozuka; Tatsuyuki Kiyozuka; Yuko Noda; Rieko Matsumura; Tetsuo Koizumi; Atsushi Watanabe; Kyosuke Nagata; Yoshinori Watanabe; Yasuhiko Terada
Journal:  J Cell Biol       Date:  2019-09-16       Impact factor: 10.539

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.