Faculty Opinions recommendation of Whole-genome screening identifies proteins localized to distinct nuclear bodies.

Author(s):  
Laura Trinkle-Mulcahy
2021 ◽  
Vol 8 (6) ◽  
pp. 3-3
Author(s):  
Sharon F. Terry

2020 ◽  
Vol 34 (10) ◽  
pp. 13776-13791
Author(s):  
Zhongzhou Si ◽  
Xinjie Guan ◽  
Xiangyun Teng ◽  
Xiaoxia Peng ◽  
Zhengqin Wan ◽  
...  

2013 ◽  
Vol 203 (1) ◽  
pp. 149-164 ◽  
Author(s):  
Ka-wing Fong ◽  
Yujing Li ◽  
Wenqi Wang ◽  
Wenbin Ma ◽  
Kunpeng Li ◽  
...  

The nucleus is a unique organelle that contains essential genetic materials in chromosome territories. The interchromatin space is composed of nuclear subcompartments, which are defined by several distinctive nuclear bodies believed to be factories of DNA or RNA processing and sites of transcriptional and/or posttranscriptional regulation. In this paper, we performed a genome-wide microscopy-based screening for proteins that form nuclear foci and characterized their localizations using markers of known nuclear bodies. In total, we identified 325 proteins localized to distinct nuclear bodies, including nucleoli (148), promyelocytic leukemia nuclear bodies (38), nuclear speckles (27), paraspeckles (24), Cajal bodies (17), Sam68 nuclear bodies (5), Polycomb bodies (2), and uncharacterized nuclear bodies (64). Functional validation revealed several proteins potentially involved in the assembly of Cajal bodies and paraspeckles. Together, these data establish the first atlas of human proteins in different nuclear bodies and provide key information for research on nuclear bodies.


2003 ◽  
Vol 73 (4) ◽  
pp. 736-747 ◽  
Author(s):  
Yaron Tomer ◽  
Yoshiyuki Ban ◽  
Erlinda Concepcion ◽  
Giuseppe Barbesino ◽  
Ronald Villanueva ◽  
...  

2001 ◽  
Vol 68 (4) ◽  
pp. 918-926 ◽  
Author(s):  
S.H. Laval ◽  
A. Timms ◽  
S. Edwards ◽  
L. Bradbury ◽  
S. Brophy ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Manuel Corpas ◽  
Karyn Megy ◽  
Vanisha Mistry ◽  
Antonio Metastasio ◽  
Edmund Lehmann

Although best practices have emerged on how to analyse and interpret personal genomes, the utility of whole genome screening remains underdeveloped. A large amount of information can be gathered from various types of analyses via whole genome sequencing including pathogenicity screening, genetic risk scoring, fitness, nutrition, and pharmacogenomic analysis. We recognize different levels of confidence when assessing the validity of genetic markers and apply rigorous standards for evaluation of phenotype associations. We illustrate the application of this approach on a family of five. By applying analyses of whole genomes from different methodological perspectives, we are able to build a more comprehensive picture to assist decision making in preventative healthcare and well-being management. Our interpretation and reporting outputs provide input for a clinician to develop a healthcare plan for the individual, based on genetic and other healthcare data.


2018 ◽  
Vol 9 (3) ◽  
Author(s):  
Marinella G. Callow ◽  
Colin Watanabe ◽  
Katherine E. Wickliffe ◽  
Russell Bainer ◽  
Sarah Kummerfield ◽  
...  

BMC Genomics ◽  
2007 ◽  
Vol 8 (1) ◽  
Author(s):  
Abdel Aouacheria ◽  
Vincent Navratil ◽  
Ricardo López-Pérez ◽  
Norma C Gutiérrez ◽  
Alexander Churkin ◽  
...  

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