Overexpression of Scg5 increases enzymatic activity of PCSK2 and is inversely correlated with body weight in congenic mice

被引:14
作者
Farber, Charles R. [1 ,4 ]
Chitwood, James [1 ]
Lee, Sang-Nam [2 ,3 ,5 ]
Verdugo, Ricardo A. [1 ]
Islas-Trejo, Alma [1 ]
Rincon, Gonzalo [1 ]
Lindberg, Iris [2 ,3 ,6 ]
Medrano, Juan F. [1 ]
机构
[1] Univ Calif Davis, Dept Anim Sci, Davis, CA 95616 USA
[2] Louisiana State Univ Hlth, Ctr Sci, Dept Biochem & Mol Biol, New Orleans, LA 70112 USA
[3] Childrens Hosp, Res Inst, New Orleans, LA 70112 USA
[4] Univ Calif Los Angeles, Div Cardiol, Dept Med, Los Angeles, CA 90095 USA
[5] Yonsei Univ, Coll Med, Res Ctr Human Nat Def Syst, Seoul 120752, South Korea
[6] Univ Maryland, Sch Med, Dept Anat & Neurobiol, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1186/1471-2156-9-34
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: The identification of novel genes is critical to understanding the molecular basis of body weight. Towards this goal, we have identified secretogranin V (Scg5; also referred to as Sgne1), as a candidate gene for growth traits. Results: Through a combination of DNA microarray analysis and quantitative PCR we identified a strong expression quantitative trait locus (eQTL) regulating Scg5 expression in two mouse chromosome 2 congenic strains and three additional F2 intercrosses. More importantly, the eQTL was coincident with a body weight QTL in congenic mice and Scg5 expression was negatively correlated with body weight in two of the F2 intercrosses. Analysis of haplotype blocks and genomic sequencing of Scg5 in high (C3H/HeJ, DBA/2J, BALB/cByJ, CAST/EiJ) and low (C57BL/6J) expressing strains revealed mutations unique to C57BL/6J and possibly responsible for the difference in mRNA abundance. To evaluate the functional consequence of Scg5 overexpression we measured the pituitary levels of 7B2 protein and PCSK2 activity and found both to be increased. In spite of this increase, the level of pituitary alpha-MSH, a PCSK2 processing product, was unaltered. Conclusion: Together, these data support a role for Scg5 in the modulation of body weight.
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页数:12
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共 39 条
[1]   Haploview: analysis and visualization of LD and haplotype maps [J].
Barrett, JC ;
Fry, B ;
Maller, J ;
Daly, MJ .
BIOINFORMATICS, 2005, 21 (02) :263-265
[2]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[3]   Impaired prohormone convertases in Cpefat/Cpefat mice [J].
Berman, Y ;
Mzhavia, N ;
Polonskaia, A ;
Devi, LA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (02) :1466-1473
[4]  
BOUGE MA, 2007, NUCLEIC ACIDS RES, V35, pD643
[5]   R/qtl: QTL mapping in experimental crosses [J].
Broman, KW ;
Wu, H ;
Sen, S ;
Churchill, GA .
BIOINFORMATICS, 2003, 19 (07) :889-890
[6]   Complex trait analysis of gene expression uncovers polygenic and pleiotropic networks that modulate nervous system function [J].
Chesler, EJ ;
Lu, L ;
Shou, SM ;
Qu, YH ;
Gu, J ;
Wang, JT ;
Hsu, HC ;
Mountz, JD ;
Baldwin, NE ;
Langston, MA ;
Threadgill, DW ;
Manly, KF ;
Williams, RW .
NATURE GENETICS, 2005, 37 (03) :233-242
[7]  
CHIU S, 2006, MOUSE BIOMEDICAL RES, V3, P816
[8]   Quantitative trait loci affecting growth in high growth (hg) mice [J].
Corva, PM ;
Horvat, S ;
Medrano, JF .
MAMMALIAN GENOME, 2001, 12 (04) :284-290
[9]   DNA binding specificity of different STAT proteins -: Comparison of in vitro specificity with natural target sites [J].
Ehret, GB ;
Reichenbach, P ;
Schindler, U ;
Horvath, CM ;
Fritz, S ;
Nabholz, M ;
Bucher, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (09) :6675-6688
[10]  
Farber CR, 2007, GENETICS, V175, P349, DOI 10.1534/genetics.106.063693