Literature DB >> 28600783

Kinetochore Malfunction in Human Pathologies.

Bas de Wolf1, Geert J P L Kops2,3,4.   

Abstract

The cell cycle culminates in mitosis with the purpose of dividing the cell's DNA content equally over two daughter cells. Error-free segregation relies on correct connections between chromosomes and spindle microtubules. Kinetochores are complex multi-protein assemblies that mediate these connections and are the platforms for attachment-error-correction and spindle assembly checkpoint signaling. Proper kinetochore function is therefore key in preventing aneuploidization. Mutations in genes encoding kinetochore proteins are associated with several severe developmental disorders associated with microcephaly, and kinetochore defects contribute to chromosomal instability in certain cancers. This chapter gives an overview of the processes necessary for faithful chromosome segregation and how kinetochore malfunction causes various human pathologies.

Entities:  

Keywords:  Aneuploidy; Cancer; Cell division; Chromosomal instability; Development; Kinetochore; Microcephaly

Mesh:

Year:  2017        PMID: 28600783     DOI: 10.1007/978-3-319-57127-0_4

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  7 in total

1.  A missense variant in NUF2, a component of the kinetochore NDC80 complex, causes impaired chromosome segregation and aneuploidy associated with microcephaly and short stature.

Authors:  Daniela Tiaki Uehara; Hiroshi Mitsubuchi; Johji Inazawa
Journal:  Hum Genet       Date:  2021-03-15       Impact factor: 4.132

Review 2.  Genetic and epigenetic effects on centromere establishment.

Authors:  Yick Hin Ling; Zhongyang Lin; Karen Wing Yee Yuen
Journal:  Chromosoma       Date:  2019-11-28       Impact factor: 4.316

3.  BUBs Are New Biomarkers of Promoting Tumorigenesis and Affecting Prognosis in Breast Cancer.

Authors:  Shunan Wang; Xinyu Liu; Meng Yang; Dongqi Yuan; Kui Ye; Xin Qu; Xinchao Wang
Journal:  Dis Markers       Date:  2022-04-21       Impact factor: 3.464

4.  Nearly complete deletion of BubR1 causes microcephaly through shortened mitosis and massive cell death.

Authors:  Ambrosia J Simmons; Raehee Park; Noelle A Sterling; Mi-Hyeon Jang; Jan M A van Deursen; Timothy J Yen; Seo-Hee Cho; Seonhee Kim
Journal:  Hum Mol Genet       Date:  2019-06-01       Impact factor: 6.150

Review 5.  The Mitotic Apparatus and Kinetochores in Microcephaly and Neurodevelopmental Diseases.

Authors:  Francesca Degrassi; Michela Damizia; Patrizia Lavia
Journal:  Cells       Date:  2019-12-24       Impact factor: 6.600

6.  ZWINT is a Promising Therapeutic Biomarker Associated with the Immune Microenvironment of Hepatocellular Carcinoma.

Authors:  Tong Lin; Yingzhao Zhang; Zhimei Lin; Lisheng Peng
Journal:  Int J Gen Med       Date:  2021-10-30

7.  Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation.

Authors:  Sara Carvalhal; Ingrid Bader; Martin A Rooimans; Anneke B Oostra; Jesper A Balk; René G Feichtinger; Christine Beichler; Michael R Speicher; Johanna M van Hagen; Quinten Waisfisz; Mieke van Haelst; Martijn Bruijn; Alexandra Tavares; Johannes A Mayr; Rob M F Wolthuis; Raquel A Oliveira; Job de Lange
Journal:  Sci Adv       Date:  2022-01-19       Impact factor: 14.136

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.