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Arch Iran Med. 2025;28(3): 140-148.
doi: 10.34172/aim.33639
  Abstract View: 4
  PDF Download: 5

Original Article

Haplogroup Structure and Genetic Variation Analyses of Mitochondrial Genome SNPs in the Iranian Population

Masoumeh Ghasemi 1 ORCID logo, Marzieh Mohseni 1, Zohreh Fattahi 1, Masoud Edizadeh 2, Maryam Beheshtian 1, Fatemeh Keshavarzi 1, Khadijeh Jalalvand 1, Mohammadamin Omrani 3, Ali Khanbazi 1,4, Yasser Riazalhosseini 5, Mohammad Reza Akbari 6, Kimia Kahrizi 1, Hossein Najmabadi 1,4* ORCID logo

1 Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
2 GENOKS Genetic Disease Diagnostic Center, Ankara 06560, Turkey
3 Urology and Nephrology Research Center (UNRC), Shahid Beheshti University of Medical Sciences, Tehran, Iran
4 Kariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran
5 Victor Phillip Dahdaleh Institute of Genomic Medicine at McGill University, Montreal, Quebec, Canada
6 Institute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, Canada
*Corresponding Author: Hossein Najmabadi, Email: hnajm12@yahoo.com

Abstract

Background: Mitochondrial DNA (mtDNA) is a valuable marker for population studies and forensic investigations. Recent advancements in massively parallel sequencing technologies enable whole mitochondrial genome sequencing. This study collected blood samples from unrelated Iranian participants from four ethnic groups: Persian, Kurd, Lur, and Azeri. We mapped mtDNA haplogroups according to genetic ancestry and investigated the ethnic similarities within the Iranian population.

Methods: Complete mtDNA sequences were generated with targeted mtDNA sequencing method and haplogroups were determined on the base of mitogenome polymorphisms. Additionally, we used data from the whole exome sequencing (WES) of the current samples to compare the variants identified by two different mitochondrial testing methods. Principal component analysis (PCA) calculations were performed using the R software to determine diversity between unrelated individuals of various ethnicities.

Results: A total of 129 sub-haplogroups were identified in 15 main haplogroups. The findings revealed high frequencies of haplogroups U and H (22.4% and 20.3%, respectively) in the Iranian population. The PCA scatter plots revealed overlapping diversity, with no distinct trends separating the groups in these four groups within the Iranian population. In the present samples, the WES method identified only 57.8% of the variants detected by the targeted mtDNA sequencing method.

Conclusion: Variant studies do not show much difference, which indicate a small genetic difference between the central ethnic groups of Iran. Furthermore, comparing the targeted whole mitochondrial genome to mitochondrial data from WES in our study samples highlights the notion that targeted entire mitochondrial genome is a gold standard method for variant detection.



Cite this article as: Ghasemi M, Mohseni M, Fattahi Z, Edizadeh M, Beheshtian M, Keshavarzi F, et al. Haplogroup structure and genetic variation analyses of mitochondrial genome SNPs in the Iranian population. Arch Iran Med. 2025;28(3):140-148. doi: 10.34172/aim.33639
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