Identification of a new quantitative trait locus on Chromosome 7 controlling disease severity of collagen-induced arthritis in rats

1999 ◽  
Vol 49 (9) ◽  
pp. 787-791 ◽  
Author(s):  
Svetlana V. Dracheva ◽  
Elaine F. Remmers ◽  
Pércio S. Gulko ◽  
Yutaka Kawahito ◽  
Ryan E. Longman ◽  
...  
2017 ◽  
Vol 243 (2) ◽  
pp. 190-197 ◽  
Author(s):  
Emmanuel Okeke ◽  
Ayotunde O Dokun

Peripheral artery disease is a major health care problem with significant morbidity and mortality. Humans with peripheral artery disease exhibit two major and differential clinical manifestations – intermittent claudication and critical limb ischemia. Individuals with intermittent claudication or critical limb ischemia have overlapping risk factors and objective measures of blood flow. Hence, we hypothesized that variation in genetic make-up may be an important determinant in the severity of peripheral artery disease. Previous studies have identified polymorphism in genes, contributing to extent of atherosclerosis but much less is known about polymorphisms associated with genes that can influence peripheral artery disease severity. This review outlines some of the progress made up-to-date to unravel the molecular mechanisms underlining differential peripheral artery disease severity. By exploring the recovery phenotype of different mouse strains following experimental peripheral artery disease, our group identified the limb salvage-associated quantitative trait locus 1 on mouse chromosome 7 as the first genetic modifier of perfusion recovery and tissue necrosis phenotypes. Furthermore, a number of genes within LSq-1, such as ADAM12, IL-21Rα, and BAG3 were identified as genetic modifiers of peripheral artery disease severity that function through preservation of endothelial and skeletal muscle cells during ischemia. Taken together, these studies suggest manipulation of limb salvage-associated quantitative trait locus 1 genes show great promise as therapeutic targets in the management of peripheral artery disease. Impact statement Peripheral artery disease (PAD) is a major health care problem with significant morbidity and mortality. Individuals with similar atherosclerosis burden do display different severity of disease. This review outlines some of the progress made up-to-date in unraveling the molecular mechanisms underlining differential PAD severity with a focus on the role of the Limb Salvage-associated Quantitative trait locus 1 (LSq-1), a key locus in adaptation to ischemia in PAD.


F1000Research ◽  
2016 ◽  
Vol 5 ◽  
pp. 2156 ◽  
Author(s):  
Wim E. Crusio ◽  
Esha Dhawan ◽  
Elissa J. Chesler ◽  
Anna Delprato

In this study we identified a quantitative trait locus (QTL) on mouse Chromosome 7 associated with locomotor activity and rearing post morphine treatment. This QTL was revealed after correcting for the effects of another QTL peak on Chromosome 10 using composite interval mapping. The positional candidate genes are Syt9 and Ppfibp2. Several other genes within the interval are linked to neural processes, locomotor activity, and the defensive response to harmful stimuli.


2006 ◽  
Vol 97 (5) ◽  
pp. 535-537 ◽  
Author(s):  
Younyoung Kim ◽  
Minyoung Kong ◽  
Yu Jin Nam ◽  
Chaeyoung Lee

2009 ◽  
Vol 61 (3) ◽  
pp. 923-934 ◽  
Author(s):  
Satoru Ishikawa ◽  
Tadashi Abe ◽  
Masato Kuramata ◽  
Masayuki Yamaguchi ◽  
Tsuyu Ando ◽  
...  

Circulation ◽  
2008 ◽  
Vol 117 (9) ◽  
pp. 1207-1215 ◽  
Author(s):  
Ayotunde O. Dokun ◽  
Sehoon Keum ◽  
Surovi Hazarika ◽  
Yongjun Li ◽  
Gregory M. Lamonte ◽  
...  

2007 ◽  
Vol 105 (2) ◽  
pp. 381-385 ◽  
Author(s):  
Michael Cascio ◽  
Yilei Xing ◽  
Diane Gong ◽  
John Popovich ◽  
Edmond I Eger ◽  
...  

F1000Research ◽  
2016 ◽  
Vol 5 ◽  
pp. 2156 ◽  
Author(s):  
Wim E. Crusio ◽  
Esha Dhawan ◽  
Elissa J. Chesler ◽  
Anna Delprato

In this study we identified a quantitative trait locus (QTL) on mouse Chromosome 7 associated with locomotor activity and rearing post morphine treatment. This QTL was revealed after correcting for the effects of another QTL peak on Chromosome 10 using composite interval mapping. The positional candidate genes are Syt9 and Ppfibp2. Several other genes within the interval are linked to neural processes, locomotor activity, and the defensive response to harmful stimuli.


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