Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009 Oct;94(4):257-62.
doi: 10.1016/j.ygeno.2009.05.008. Epub 2009 May 29.

Differentially expressed genes strongly correlated with femur strength in rats

Affiliations

Differentially expressed genes strongly correlated with femur strength in rats

Imranul Alam et al. Genomics. 2009 Oct.

Abstract

The region of chromosome 1q33-q54 harbors quantitative trait loci (QTL) for femur strength in COPxDA and F344xLEW F2 rats. The purpose of this study is to identify the genes within this QTL region that contribute to the variation in femur strength. Microarray analysis was performed using RNA extracted from femurs of COP, DA, F344 and LEW rats. Genes differentially expressed in the 1q33-q54 region among these rat strains were then ranked based on the strength of correlation with femur strength in F2 animals derived from these rats. A total of 214 genes in this QTL region were differentially expressed among all rat strains, and 81 genes were found to be strongly correlated (r(2)>0.50) with femur strength. Of these, 12 candidate genes were prioritized for further validation, and 8 of these genes (Ifit3, Ppp2r5b, Irf7, Mpeg1, Bloc1s2, Pycard, Sec23ip, and Hps6) were confirmed by quantitative PCR (qPCR). Ingenuity Pathway Analysis suggested that these genes were involved in interferon alpha, nuclear factor-kappa B (NFkB), extracellular signal-related kinase (ERK), hepatocyte nuclear factor 4 alpha (HNF4A) and tumor necrosis factor (TNF) pathways.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Linkage analysis for femur ultimate force (Fu) for rat chromosome 1 in COP×DA and F344×LEW crosses in the region of 1q33–q54 (D1Rat52–D1Rat82). LOD scores plotted on the y axis vs. the relative microsatellite markers located along chromosome 1 on the x axis.
Fig. 2
Fig. 2
Network of the 8 candidate genes that were confirmed by qPCR (highlighted in red) for femur strength in Ingenuity Pathway Analysis (IPA). The well-known NFkB, ERK and TNF pathways related to bone metabolism is highlighted in blue.

Similar articles

Cited by

References

    1. Kanis JA, Melton LJ, Christiansen C, Johnston CC, Khaltaev N. The diagnosis of osteoporosis. J. Bone. Miner. Res. 1994;9:1137–1141. - PubMed
    1. Cummings SR, Black DM, Nevitt MC, Browner W, Cauley J, Ensrud K, Genant HK, Palermo L, Scott J, Vogt TM. Bone density at various sites for prediction of hip fractures, The Study of Osteoporotic Fractures Research Group. Lancet. 1993;341:72–75. - PubMed
    1. Faulkner KG, Cummings SR, Black D, Palermo L, Gluer CC, Genant HK. Simple measurement of femoral geometry predicts hip fracture: the study of osteoporotic fractures. J. Bone. Miner. Res. 1993;8:1211–1217. - PubMed
    1. Peacock M, Turner CH, Liu G, Manatunga AK, Timmerman L, Johnston CC. Better discrimination of hip fracture using bone density, geometry and architecture. Osteoporos. Int. 1995;5:167–173. - PubMed
    1. Arden NK, Baker J, Hogg C, Bann K, Spector TD. The heritability of bone mineral density, ultrasound of the calcaneus and hip axis length: a study of postmenopausal twins. J. Bone Miner. Res. 1996;11:530–534. - PubMed

Publication types

MeSH terms