Influence of missense mutation and silent mutation of LHbeta-subunit gene in Japanese patients with ovulatory disorders

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This study found specific silent mutations in the LHbeta gene were more frequent in Japanese patients with ovulatory disorders, potentially influencing missense mutations and contributing to these conditions.

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This study investigated the frequency of two missense mutations and five silent mutations in the luteinizing hormone (LH) β-subunit gene (LHβ) and tested their association with ovulatory disorders in Japanese participants. Using PCR amplification and sequence comparison to a reported wild-type LHβ base sequence, the authors analyzed 43 patients with ovulatory disorders, 79 with normal ovulatory cycles, and 23 healthy men, finding the highest frequency of a novel allele at C1036–A and higher frequencies of several novel alleles (including C894–T, C1098–T, and C1423–T) in patients with ovulatory disorders than in those with normal cycles. They reported that no wild-type homozygotes for LHβ (C1036) were identified and that silent mutations among patients with variant LH were more prevalent in ovulatory disorders than in normal ovulatory cycles, while noting that silent mutations might influence missense mutations and/or other unknown missense mutations. Relevance to endometriosis: the paper reports that the frequency of novel alleles differed from healthy women in patients including those with endometriosis, though its main focus is genetic variation in the LHβ gene and ovulatory disorders.

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Abstract

The frequency of variant LHbeta containing two point mutations (T(986)-C and T(1008)-C) and its relationship to reproductive disorders differ widely between ethnic groups. In a Japanese population, variant luteinizing hormone (LH) correlates with ovulatory disorders. Here we examined the relationship between two missense mutations and five silent mutations (C(894)-T, G(1018)-C, C(1036)-A, C(1098)-T and C(1423)-T) in the LHbeta gene, and ovulatory disorders. We studied 43 patients with ovulatory disorders, 79 patients with normal ovulatory cycles, and 23 healthy men who agreed to join our DNA analysis. PCR-amplified LHbeta-subunit gene sequences were compared with a base sequence of wild-type LH reported after direct sequencing. The highest frequency (0.945) of novel allele was observed at the position of the C(1036)-A transition. No homozygotes for wild-type LHbeta (C(1036)) were identified. The frequency of novel allele in patients with polycystic ovary syndrome, endometriosis, premature ovarian failure and luteal insufficiency was significantly different from that of healthy women. The frequencies of novel alleles (C(894)-T, C(1098)-T and C(1423)-T) in patients with ovulatory disorders were significantly higher than those with normal ovulatory cycles. The mean incidence of point mutation in patients with ovulatory disorders was higher than in those with normal ovulatory cycles. Among patients with variant LH, five silent mutations were identified in 87.5% of patients with ovulatory disorders, whereas only a few silent mutations were identified in patients with normal ovulatory cycles. In a Japanese population, five silent mutations of variant LH could have influenced two missense mutations and/or other unknown missense mutations, causing ovulatory disorders.
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Abstract

The frequency of variant LHβ containing two point mutations (T986–C and T1008–C) and its relationship to reproductive disorders differ widely between ethnic groups. In a Japanese population, variant luteinizing hormone (LH) correlates with ovulatory disorders. Here we examined the relationship between two missense mutations and five silent mutations (C894–T, G1018–C, C1036–A, C1098-T and C1423–T) in the LHβ gene, and ovulatory disorders. We studied 43 patients with ovulatory disorders, 79 patients with normal ovulatory cycles, and 23 healthy men who agreed to join our DNA analysis. PCR-amplified LHβ-subunit gene sequences were compared with a base sequence of wild-type LH reported after direct sequencing. The highest frequency (0.945) of novel allele was observed at the position of the C1036–A transition. No homozygotes for wild-type LHβ (C1036) were identified. The frequency of novel allele in patients with polycystic ovary syndrome, endometriosis, premature ovarian failure and luteal insufficiency was significantly different from that of healthy women. The frequencies of novel alleles (C894–T, C1098–T and C1423–T) in patients with ovulatory disorders were significantly higher than those with normal ovulatory cycles. The mean incidence of point mutation in patients with ovulatory disorders was higher than in those with normal ovulatory cycles. Among patients with variant LH, five silent mutations were identified in 87.5% of patients with ovulatory disorders, whereas only a few silent mutations were identified in patients with normal ovulatory cycles. In a Japanese population, five silent mutations of variant LH could have influenced two missense mutations and/or other unknown missense mutations, causing ovulatory disorders. Similar content being viewed by others Log in or create a free account to read this content Gain free access to this article, as well as selected content from this journal and more on nature.com or

References

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This article is cited by - A brief insight into the etiology, genetics, and immunology of polycystic ovarian syndrome (PCOS) Journal of Assisted Reproduction and Genetics (2022)

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endometriosis

MeSH descriptors

Luteinizing Hormone, beta Subunit Mutation, Missense Ovarian Diseases Endometriosis Endometriosis Female Gene Frequency Humans Japan Luteinizing Hormone, beta Subunit Male Ovarian Diseases Sequence Analysis, DNA

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