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
. 2021 Jun 16:12:678374.
doi: 10.3389/fgene.2021.678374. eCollection 2021.

Ethnic Differences in the Frequency of CFTR Gene Mutations in Populations of the European and North Caucasian Part of the Russian Federation

Affiliations

Ethnic Differences in the Frequency of CFTR Gene Mutations in Populations of the European and North Caucasian Part of the Russian Federation

Nika Petrova et al. Front Genet. .

Abstract

Cystic fibrosis (CF) is a common monogenic disease caused by pathogenic variants in the CFTR gene. The distribution and frequency of CFTR variants vary in different countries and ethnic groups. The spectrum of pathogenic variants of the CFTR gene was previously studied in more than 1,500 CF patients from different regions of the European and North Caucasian region of Russia and the spectrum of the most frequent pathogenic variants of the CFTR gene and ethnic features of their distribution were determined. To assess the population frequency of CFTR gene mutations some of the common variants were analyzed in the samples of healthy unrelated individuals from the populations of the European part of the Russian Federation: 1,324 Russians from four European regions (Pskov, Tver, Rostov, and Kirov regions), representatives of five indigenous ethnic groups of the Volga-Ural region [Mari (n = 505), Udmurts (n = 613), Chuvash (n = 780), Tatars (n = 704), Bashkirs (n = 517)], and six ethnic groups of the North Caucasus [Karachay (n = 324), Nogais (n = 118), Circassians (n = 102), Abazins (n = 128), Ossetians (n = 310), and Chechens (n = 100)]. The frequency of common CFTR mutations was established in studied ethnic groups. The frequency of F508del mutation in Russians was found to be 0.0056 on average, varying between four regions, from 0.0027 in the Pskov region to 0.0069 in the Rostov region. Three variants W1282X, 1677delTA, and F508del were identified in the samples from the North Caucasian populations: in Karachay, the frequency of W1282X mutation was 0.0092, 1677delTA mutation - 0.0032; W1282X mutation in the Nogais sample - 0.0127, the frequency of F508del mutations was 0.0098 and 1677delTA - 0.0098 in Circassians; in Abazins F508del (0.0039), W1282X (0.0039) and 1677delTA (0.0117) mutations were found. In the indigenous peoples of the Volga-Ural region, the maximum frequency of the F508del mutation was detected in the Tatar population (0.099), while this mutation was never detected in the Mari and Bashkir populations. The E92K variant was found in Chuvash and Tatar populations. Thus, interethnic differences in the spectra of CFTR gene variants were shown both in CF patients and in healthy population of the European and North Caucasian part of Russia.

Keywords: CFTR gene variants; European and North Caucasian part of Russia; allelic polymorphism; ethnic diversity; population differences.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Relative frequencies of common CFTR variants in studied regions and ethnic groups of European part and North Caucasus of Russia.
FIGURE 2
FIGURE 2
Location of studied populations. Russians – Pskov, Tver, Kirov, Rostov-on-Don. Volga-Ural region: Yoshkar-Ola – Mari; Cheboksary – Chuvashes; Kazan – Bashkirs; Izhevsk – Udmurts; Ufa – Bashkirs. North Caucasus region: Inzhich-Chukum – Abaza; Erken-Shakar – Nogais; Khabez – Circassians; Karachaevsk – Karachay; Vladikavkaz – Ossetians; Grozny – Chechens.
FIGURE 3
FIGURE 3
Distribution of CFTR variant frequencies in European populations. The radii of the circles reflect the frequency values.

Similar articles

Cited by

References

    1. Abramov D. D., Kadochnikova V. V., Yakimova E. G., Belousova M. V., Maerle A. V., Sergeev I. V., et al. (2015). High carrier frequency of CFTR gene mutations associated with cystic fibrosis, and PAH gene mutations associated with phenylketonuria in Russian population. VESTNIK RGMU.RU 4 32–35.
    1. Alekseev V. (1974). The Geography of Human Races, 1st Edn. Moscow: Nauka.
    1. Atag E., Ikizoglu N. B., Ergenekon A. P., Gokdemir Y., Eralp E. E., Ata P., et al. (2019). Novel mutations and deletions in cystic fibrosis in a tertiary cystic fibrosis center in Istanbul. Pediatr. Pulmonol. 54 743–750. 10.1002/ppul.24299 - DOI - PubMed
    1. Bobadilla J. L., Macek M., Jr., Fine J. P., Farrell P. M. (2002). Cystic fibrosis: a worldwide analysis of CFTR mutations - correlation with incidence data and application to screening. Hum. Mutat. 19 575–606. 10.1002/humu.10041 - DOI - PubMed
    1. Brandt N. J., Schwartz M., Skovby F. (1994). Screening for carriers of cystic fibrosis. result of a pilot study among pregnant women. Ugeskr. Laeger 156 3751–3757. - PubMed