Follicle-stimulating hormone beta gene structure in premature ovarian failure

Lawrence C Layman, M. E. Shelley, L. O. Huey, S. W. Wall, S. P.T. Tho, Paul G McDonough

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Objective: To determine whether mutations in the gene for FSHβ are present, and possibly etiologic, in some patients with 46,XX premature ovarian failure (POF). Design: DNA samples obtained from 18 study patients with POF and two menopausal fertile controls were studied by Southern blot analysis. DNA sequencing was performed in one patient. Setting: Patients were seen in a reproductive endocrinology clinic and studied in a medical school laboratory setting at the Medical College of Georgia and Tufts University. Main Outcome Measures: Restriction fragment sizes on autoradiographs were compared between the study group and controls. DNA sequencing radiographs were compared between one study patient and five controls. Results: Fragment sizes obtained with the restriction enzymes EcoRI, DraI, HincII, PstI, KpnI, BglI, BamHI, and BglII were similar size in both study subjects and controls using the probes pFSHβ-1.4 and pFSHβ-1.2. A previously described HindIII polymorphism was present using pFSHβ-1.2, but HindIII fragment sizes were identical in patients with ovarian failure and controls using pFSHβ-1.4. DNA sequencing of the FSHβ gene in one patient was normal. Conclusions: No mutations in the gene for FSHβ were identified in women with POF. DNA sequencing of the exons and promoter region of the FSHβ gene in one woman with POF was normal. This does not entirely exclude the possibility that smaller deletions, insertions, or point mutations of the FSHβ could be etiologic in some women with POF. The HindIII polymorphism does not appear to segregate with 46,XX POF.

Original languageEnglish (US)
Pages (from-to)852-857
Number of pages6
JournalFertility and Sterility
Volume60
Issue number5
DOIs
StatePublished - Jan 1 1993

Fingerprint

Primary Ovarian Insufficiency
Follicle Stimulating Hormone
DNA Sequence Analysis
Genes
Mutation
Sequence Deletion
Endocrinology
Insertional Mutagenesis
Southern Blotting
Medical Schools
Point Mutation
Genetic Promoter Regions
Exons
Outcome Assessment (Health Care)
Control Groups
DNA
Enzymes

Keywords

  • FSH
  • FSH- beta
  • Premature ovarian failure
  • chromosomally competent ovarian failure
  • gene
  • molecular genetics

ASJC Scopus subject areas

  • Reproductive Medicine
  • Obstetrics and Gynecology

Cite this

Layman, L. C., Shelley, M. E., Huey, L. O., Wall, S. W., Tho, S. P. T., & McDonough, P. G. (1993). Follicle-stimulating hormone beta gene structure in premature ovarian failure. Fertility and Sterility, 60(5), 852-857. https://doi.org/10.1016/S0015-0282(16)56286-4

Follicle-stimulating hormone beta gene structure in premature ovarian failure. / Layman, Lawrence C; Shelley, M. E.; Huey, L. O.; Wall, S. W.; Tho, S. P.T.; McDonough, Paul G.

In: Fertility and Sterility, Vol. 60, No. 5, 01.01.1993, p. 852-857.

Research output: Contribution to journalArticle

Layman, Lawrence C ; Shelley, M. E. ; Huey, L. O. ; Wall, S. W. ; Tho, S. P.T. ; McDonough, Paul G. / Follicle-stimulating hormone beta gene structure in premature ovarian failure. In: Fertility and Sterility. 1993 ; Vol. 60, No. 5. pp. 852-857.
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abstract = "Objective: To determine whether mutations in the gene for FSHβ are present, and possibly etiologic, in some patients with 46,XX premature ovarian failure (POF). Design: DNA samples obtained from 18 study patients with POF and two menopausal fertile controls were studied by Southern blot analysis. DNA sequencing was performed in one patient. Setting: Patients were seen in a reproductive endocrinology clinic and studied in a medical school laboratory setting at the Medical College of Georgia and Tufts University. Main Outcome Measures: Restriction fragment sizes on autoradiographs were compared between the study group and controls. DNA sequencing radiographs were compared between one study patient and five controls. Results: Fragment sizes obtained with the restriction enzymes EcoRI, DraI, HincII, PstI, KpnI, BglI, BamHI, and BglII were similar size in both study subjects and controls using the probes pFSHβ-1.4 and pFSHβ-1.2. A previously described HindIII polymorphism was present using pFSHβ-1.2, but HindIII fragment sizes were identical in patients with ovarian failure and controls using pFSHβ-1.4. DNA sequencing of the FSHβ gene in one patient was normal. Conclusions: No mutations in the gene for FSHβ were identified in women with POF. DNA sequencing of the exons and promoter region of the FSHβ gene in one woman with POF was normal. This does not entirely exclude the possibility that smaller deletions, insertions, or point mutations of the FSHβ could be etiologic in some women with POF. The HindIII polymorphism does not appear to segregate with 46,XX POF.",
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AU - Tho, S. P.T.

AU - McDonough, Paul G

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N2 - Objective: To determine whether mutations in the gene for FSHβ are present, and possibly etiologic, in some patients with 46,XX premature ovarian failure (POF). Design: DNA samples obtained from 18 study patients with POF and two menopausal fertile controls were studied by Southern blot analysis. DNA sequencing was performed in one patient. Setting: Patients were seen in a reproductive endocrinology clinic and studied in a medical school laboratory setting at the Medical College of Georgia and Tufts University. Main Outcome Measures: Restriction fragment sizes on autoradiographs were compared between the study group and controls. DNA sequencing radiographs were compared between one study patient and five controls. Results: Fragment sizes obtained with the restriction enzymes EcoRI, DraI, HincII, PstI, KpnI, BglI, BamHI, and BglII were similar size in both study subjects and controls using the probes pFSHβ-1.4 and pFSHβ-1.2. A previously described HindIII polymorphism was present using pFSHβ-1.2, but HindIII fragment sizes were identical in patients with ovarian failure and controls using pFSHβ-1.4. DNA sequencing of the FSHβ gene in one patient was normal. Conclusions: No mutations in the gene for FSHβ were identified in women with POF. DNA sequencing of the exons and promoter region of the FSHβ gene in one woman with POF was normal. This does not entirely exclude the possibility that smaller deletions, insertions, or point mutations of the FSHβ could be etiologic in some women with POF. The HindIII polymorphism does not appear to segregate with 46,XX POF.

AB - Objective: To determine whether mutations in the gene for FSHβ are present, and possibly etiologic, in some patients with 46,XX premature ovarian failure (POF). Design: DNA samples obtained from 18 study patients with POF and two menopausal fertile controls were studied by Southern blot analysis. DNA sequencing was performed in one patient. Setting: Patients were seen in a reproductive endocrinology clinic and studied in a medical school laboratory setting at the Medical College of Georgia and Tufts University. Main Outcome Measures: Restriction fragment sizes on autoradiographs were compared between the study group and controls. DNA sequencing radiographs were compared between one study patient and five controls. Results: Fragment sizes obtained with the restriction enzymes EcoRI, DraI, HincII, PstI, KpnI, BglI, BamHI, and BglII were similar size in both study subjects and controls using the probes pFSHβ-1.4 and pFSHβ-1.2. A previously described HindIII polymorphism was present using pFSHβ-1.2, but HindIII fragment sizes were identical in patients with ovarian failure and controls using pFSHβ-1.4. DNA sequencing of the FSHβ gene in one patient was normal. Conclusions: No mutations in the gene for FSHβ were identified in women with POF. DNA sequencing of the exons and promoter region of the FSHβ gene in one woman with POF was normal. This does not entirely exclude the possibility that smaller deletions, insertions, or point mutations of the FSHβ could be etiologic in some women with POF. The HindIII polymorphism does not appear to segregate with 46,XX POF.

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