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Review
. 2022 Aug 1;10(8):1855.
doi: 10.3390/biomedicines10081855.

Genetic Modifications to Alter Blood Pressure Level

Affiliations
Review

Genetic Modifications to Alter Blood Pressure Level

Hiroki Ohara et al. Biomedicines. .

Abstract

Genetic manipulation is one of the indispensable techniques to examine gene functions both in vitro and in vivo. In particular, cardiovascular phenotypes such as blood pressure cannot be evaluated in vitro system, necessitating the creation of transgenic or gene-targeted knock-out and knock-in experimental animals to understand the pathophysiological roles of specific genes on the disease conditions. Although genome-wide association studies (GWAS) in various human populations have identified multiple genetic variations associated with increased risk for hypertension and/or its complications, the causal links remain unresolved. Genome-editing technologies can be applied to many different types of cells and organisms for creation of knock-out/knock-in models. In the post-GWAS era, it may be more worthwhile to validate pathophysiological implications of the risk variants and/or candidate genes by creating genome-edited organisms.

Keywords: Dahl SS; SHR; SHRSP; genome-editing; knock-out.

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Conflict of interest statement

The authors declare no conflict of interest.

References

    1. Zhou B., Carrillo-Larco R.M., Danaei G., Riley L.M., Paciorek C.J., Stevens G.A., Gregg E.W., Bennett J.E., Solomon B., Singleton R.K., et al. Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: A pooled analysis of 1201 population-representative studies with 104 million participants. Lancet. 2021;398:957–980. doi: 10.1016/S0140-6736(21)01330-1. - DOI - PMC - PubMed
    1. Mashimo T. Gene targeting technologies in rats: Zinc finger nucleases, transcription activator-like effector nucleases, and clustered regularly interspaced short palindromic repeats. Dev. Growth Differ. 2014;56:46–52. doi: 10.1111/dgd.12110. - DOI - PubMed
    1. Kaneko T., Mashimo T. Simple Genome Editing of Rodent Intact Embryos by Electroporation. PLoS ONE. 2015;10:e0142755. doi: 10.1371/journal.pone.0142755. - DOI - PMC - PubMed
    1. Stegbauer J., Chen D., Herrera M., Sparks M.A., Yang T., Konigshausen E., Gurley S.B., Coffman T.M. Resistance to hypertension mediated by intercalated cells of the collecting duct. JCI Insight. 2017;2:e92720. doi: 10.1172/jci.insight.92720. - DOI - PMC - PubMed
    1. Li X.C., Leite A.P.O., Zheng X., Zhao C., Chen X., Zhang L., Zhou X., Rubera I., Tauc M., Zhuo J.L. Proximal Tubule-Specific Deletion of Angiotensin II Type 1a Receptors in the Kidney Attenuates Circulating and Intratubular Angiotensin II-Induced Hypertension in PT-Agtr1a−/− Mice. Hypertension. 2021;77:1285–1298. doi: 10.1161/HYPERTENSIONAHA.120.16336. - DOI - PMC - PubMed

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