Evidence map›Paper›PMID 36115009›Full record

ArticleGenes & genomics2023

The infertile individual analysis based on whole-exome sequencing in chinese multi-ethnic groups.

Qiongzhen Zhao, Yanqi Li, Qi Liang, Jie Zhao, Kai Kang, Meiling Hou, Xin Zhang, Renqian Du, Lingyin Kong, Bo Liang and 1 more

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Article in Genes & genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Qiongzhen ZhaoTanzhi Stem Cell Bank of Xinjiang, 844000, Tumshuk, Xinjiang, China.
Yanqi LiTanzhi Stem Cell Bank of Xinjiang, 844000, Tumshuk, Xinjiang, China.
Qi LiangXinjiang Jiayin hospital, 830000, Urumqi, Xinjiang, China.
Jie ZhaoXinjiang Jiayin hospital, 830000, Urumqi, Xinjiang, China.
Kai KangBasecare Medical Device Co., Ltd, 215001, Suzhou, Jiangsu, China.
Meiling HouSuzhou BioX Research Institute, 215001, Suzhou, Jiangsu, China.
Xin ZhangBasecare Medical Device Co., Ltd, 215001, Suzhou, Jiangsu, China.
Renqian DuBasecare Medical Device Co., Ltd, 215001, Suzhou, Jiangsu, China.
Lingyin KongBasecare Medical Device Co., Ltd, 215001, Suzhou, Jiangsu, China.
Bo LiangState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic and Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 200020, Shanghai, China. boliang880@alumni.sjtu.edu.cn.
Weidong HuangTanzhi Stem Cell Bank of Xinjiang, 844000, Tumshuk, Xinjiang, China. hwd@jynk.com.
Shanghai Jiao Tong University · CNSuzhou Research Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfertility is a common and rapidly growing health issue around the world. The genetic analysis based on the infertile population is crucial for intervention and treatment.

objectiveTo find candidate gene locus led to azoospermia in Chinese multi-ethnic groups and provide theoretical guidance for the diagnosis of genetic diseases to progressively aggravated infertility patients and sterile offspring with ART.

methodsThe study based on whole-exome sequencing (WES) was presented for genetic characteristic analysis of multi-ethnics and identification of variants related to infertility in Xinjiang area of China.

resultsThe frequency of pathogenic variants showed significant ethnic differences among four main ethnics in Xinjiang. The population structure analysis confirmed that the Hui was close to the Han population, the Kazak was close to the Uygur population, and there are three ancestry components in the four ethnics. In addition, ten candidate variants potentially regulated azoospermia were detected, and KNTC1 (rs7968222: G > T) was chosen to validate the association. Through the analysis in the valid group, the frequency of rs7968222 (G > T) has a significant difference in the azoospermia population (11.76%, 8/68) and normospermia population (4.63%, 35/756) (P < 0.001). Interestingly, the proportion of people with abnormal follicle-stimulating hormone (FSH) level in the group carrying rs7968222 (G > T) was significantly higher than non-carriers (P < 0.05). Therefore, rs7968222 may regulate spermatogenesis through affecting hormone level.

conclusionOur study establishes the genetics analysis of Northwest China and finds a candidate gene locus KNTC1 (rs7968222: G > T), which is one of the genetic susceptibility factors for male azoospermia.

Indexed as

AzoospermiaCell Cycle ProteinsMicrotubule-Associated ProteinsEast Asian PeopleEthnicityExome SequencingGenetic Predisposition to DiseaseHumansMaleCell Cycle ProteinsKNTC1 protein, humanMicrotubule-Associated ProteinsAzoospermiaGenetic data analysisInfertilityWhole exon sequencing

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PMID36115009
OpenAlexW4296129421

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