Literature DB >> 27389988

Nucleoporin gene expression in Xenopus tropicalis embryonic development.

Nooreen Reza1, Mustafa K Khokha, Florencia Del Viso.   

Abstract

Nucleoporins (nups) compose the structure of the nuclear pore complex (NPC) of all cells, but several studies have illuminated nucleoporins' additional roles in development and the cell cycle. However, a comprehensive study of nup expression in embryonic development has not yet been reported. We synthesized antisense probes for all nup genes and used whole-mount in situ hybridization techniques to determine the expression pattern of all members of the nup family of genes at three different developmental stages in Xenopus tropicalis. We found that the expression of nups was not ubiquitous in embryos, but was localized to specific and distinguishable anatomical structures at all three stages tested. We also found that the expression patterns for nups within the same subcomplexes were not necessarily identical. Thus, nup expression is subject to a significant level of regulation during development. These results provide new information for functional studies of nups to unravel their roles in embryonic development.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27389988     DOI: 10.1387/ijdb.150317nr

Source DB:  PubMed          Journal:  Int J Dev Biol        ISSN: 0214-6282            Impact factor:   2.203


  3 in total

1.  Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia.

Authors:  Florencia Del Viso; Fang Huang; Jordan Myers; Madeleine Chalfant; Yongdeng Zhang; Nooreen Reza; Joerg Bewersdorf; C Patrick Lusk; Mustafa K Khokha
Journal:  Dev Cell       Date:  2016-09-01       Impact factor: 12.270

2.  Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome.

Authors:  Daniela A Braun; Svjetlana Lovric; David Schapiro; Ronen Schneider; Jonathan Marquez; Maria Asif; Muhammad Sajid Hussain; Ankana Daga; Eugen Widmeier; Jia Rao; Shazia Ashraf; Weizhen Tan; C Patrick Lusk; Amy Kolb; Tilman Jobst-Schwan; Johanna Magdalena Schmidt; Charlotte A Hoogstraten; Kaitlyn Eddy; Thomas M Kitzler; Shirlee Shril; Abubakar Moawia; Kathrin Schrage; Arwa Ishaq A Khayyat; Jennifer A Lawson; Heon Yung Gee; Jillian K Warejko; Tobias Hermle; Amar J Majmundar; Hannah Hugo; Birgit Budde; Susanne Motameny; Janine Altmüller; Angelika Anna Noegel; Hanan M Fathy; Daniel P Gale; Syeda Seema Waseem; Ayaz Khan; Larissa Kerecuk; Seema Hashmi; Nilufar Mohebbi; Robert Ettenger; Erkin Serdaroğlu; Khalid A Alhasan; Mais Hashem; Sara Goncalves; Gema Ariceta; Mercedes Ubetagoyena; Wolfram Antonin; Shahid Mahmood Baig; Fowzan S Alkuraya; Qian Shen; Hong Xu; Corinne Antignac; Richard P Lifton; Shrikant Mane; Peter Nürnberg; Mustafa K Khokha; Friedhelm Hildebrandt
Journal:  J Clin Invest       Date:  2018-09-04       Impact factor: 14.808

3.  Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders.

Authors:  Ethiraj Ravindran; Ramona Jühlen; Carlos H Vieira-Vieira; Thuong Ha; Yuval Salzberg; Boris Fichtman; Lena Luise-Becker; Nuno Martins; Sylvie Picker-Minh; Paraskevi Bessa; Peer Arts; Matilda R Jackson; Ajay Taranath; Benjamin Kamien; Christopher Barnett; Na Li; Victor Tarabykin; Gisela Stoltenburg-Didinger; Amnon Harel; Matthias Selbach; Achim Dickmanns; Birthe Fahrenkrog; Hao Hu; Hamish Scott; Angela M Kaindl
Journal:  Hum Mol Genet       Date:  2021-11-01       Impact factor: 5.121

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.