Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Ning Xu, Hyung Goo Kim, Balasubramanian Bhagavath, Sung Gyu Cho, Jae Ho Lee, Kyungsoo Ha, Irene Meliciani, Wolfgang Wenzel, Robert H. Podolsky, Lynn P. Chorich, Kathryn A. Stackhouse, Anna M.H. Grove, Lawrence N. Odom, Metin Ozata, David P. Bick, Richard J. Sherins, Soo Hyun Kim, Richard S Cameron, Lawrence C Layman

Research output: Contribution to journalArticle

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Abstract

Objective: To determine if mutations in NELF, a gene isolated from migratory GnRH neurons, cause normosmic idiopathic hypogonadotropic hypogonadism (IHH) and Kallmann syndrome (KS). Design: Molecular analysis correlated with phenotype. Setting: Academic medical center. Patient(s): A total of 168 IHH/KS patients as well as unrelated control subjects were studied for NELF mutations. Intervention(s): NELF coding regions/splice junctions were subjected to polymerase chain reaction (PCR)-based DNA sequencing. Eleven additional IHH/KS genes were sequenced in three patients with NELF mutations. Main Outcome Measure(s): Mutations were confirmed by sorting intolerant from tolerant, reverse-transcription (RT)-PCR, and Western blot analysis. Result(s): Three novel NELF mutations absent in 372 ethnically matched control subjects were identified in 3/168 (1.8%) IHH/KS patients. One IHH patient had compound heterozygous NELF mutations (c.629-21G>C and c.629-23C>G), and he did not have mutations in 11 other known IHH/KS genes. Two unrelated KS patients had heterozygous NELF mutations and mutation in a second gene: NELF/KAL1 (c.757G>A; p.Ala253Thr of NELF and c.488-490delGTT; p.Cys163del of KAL1) and NELF/TACR3 (c.1160-13C>T of NELF and c.824G>A; p.Trp275X of TACR3). In vitro evidence of these NELF mutations included reduced protein expression and splicing defects. Conclusion(s): Our findings suggest that NELF is associated with normosmic IHH and KS, either singly or in combination with a mutation in another gene.

Original languageEnglish (US)
JournalFertility and sterility
Volume95
Issue number5
DOIs
StatePublished - Jan 1 2011

Fingerprint

Kallmann Syndrome
Hypogonadism
Nose
Gonadotropin-Releasing Hormone
Mutation
Genes
Protein Splicing
Polymerase Chain Reaction

Keywords

  • GnRH neuron migration
  • Kallmann syndrome
  • Nasal embryonic LHRH factor
  • gonadotropin-releasing hormone (GnRH)
  • hypogonadotropic hypogonadism

ASJC Scopus subject areas

  • Reproductive Medicine
  • Obstetrics and Gynecology

Cite this

Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome. / Xu, Ning; Kim, Hyung Goo; Bhagavath, Balasubramanian; Cho, Sung Gyu; Lee, Jae Ho; Ha, Kyungsoo; Meliciani, Irene; Wenzel, Wolfgang; Podolsky, Robert H.; Chorich, Lynn P.; Stackhouse, Kathryn A.; Grove, Anna M.H.; Odom, Lawrence N.; Ozata, Metin; Bick, David P.; Sherins, Richard J.; Kim, Soo Hyun; Cameron, Richard S; Layman, Lawrence C.

In: Fertility and sterility, Vol. 95, No. 5, 01.01.2011.

Research output: Contribution to journalArticle

Xu, N, Kim, HG, Bhagavath, B, Cho, SG, Lee, JH, Ha, K, Meliciani, I, Wenzel, W, Podolsky, RH, Chorich, LP, Stackhouse, KA, Grove, AMH, Odom, LN, Ozata, M, Bick, DP, Sherins, RJ, Kim, SH, Cameron, RS & Layman, LC 2011, 'Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome', Fertility and sterility, vol. 95, no. 5. https://doi.org/10.1016/j.fertnstert.2011.01.010
Xu, Ning ; Kim, Hyung Goo ; Bhagavath, Balasubramanian ; Cho, Sung Gyu ; Lee, Jae Ho ; Ha, Kyungsoo ; Meliciani, Irene ; Wenzel, Wolfgang ; Podolsky, Robert H. ; Chorich, Lynn P. ; Stackhouse, Kathryn A. ; Grove, Anna M.H. ; Odom, Lawrence N. ; Ozata, Metin ; Bick, David P. ; Sherins, Richard J. ; Kim, Soo Hyun ; Cameron, Richard S ; Layman, Lawrence C. / Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome. In: Fertility and sterility. 2011 ; Vol. 95, No. 5.
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AU - Kim, Hyung Goo

AU - Bhagavath, Balasubramanian

AU - Cho, Sung Gyu

AU - Lee, Jae Ho

AU - Ha, Kyungsoo

AU - Meliciani, Irene

AU - Wenzel, Wolfgang

AU - Podolsky, Robert H.

AU - Chorich, Lynn P.

AU - Stackhouse, Kathryn A.

AU - Grove, Anna M.H.

AU - Odom, Lawrence N.

AU - Ozata, Metin

AU - Bick, David P.

AU - Sherins, Richard J.

AU - Kim, Soo Hyun

AU - Cameron, Richard S

AU - Layman, Lawrence C

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N2 - Objective: To determine if mutations in NELF, a gene isolated from migratory GnRH neurons, cause normosmic idiopathic hypogonadotropic hypogonadism (IHH) and Kallmann syndrome (KS). Design: Molecular analysis correlated with phenotype. Setting: Academic medical center. Patient(s): A total of 168 IHH/KS patients as well as unrelated control subjects were studied for NELF mutations. Intervention(s): NELF coding regions/splice junctions were subjected to polymerase chain reaction (PCR)-based DNA sequencing. Eleven additional IHH/KS genes were sequenced in three patients with NELF mutations. Main Outcome Measure(s): Mutations were confirmed by sorting intolerant from tolerant, reverse-transcription (RT)-PCR, and Western blot analysis. Result(s): Three novel NELF mutations absent in 372 ethnically matched control subjects were identified in 3/168 (1.8%) IHH/KS patients. One IHH patient had compound heterozygous NELF mutations (c.629-21G>C and c.629-23C>G), and he did not have mutations in 11 other known IHH/KS genes. Two unrelated KS patients had heterozygous NELF mutations and mutation in a second gene: NELF/KAL1 (c.757G>A; p.Ala253Thr of NELF and c.488-490delGTT; p.Cys163del of KAL1) and NELF/TACR3 (c.1160-13C>T of NELF and c.824G>A; p.Trp275X of TACR3). In vitro evidence of these NELF mutations included reduced protein expression and splicing defects. Conclusion(s): Our findings suggest that NELF is associated with normosmic IHH and KS, either singly or in combination with a mutation in another gene.

AB - Objective: To determine if mutations in NELF, a gene isolated from migratory GnRH neurons, cause normosmic idiopathic hypogonadotropic hypogonadism (IHH) and Kallmann syndrome (KS). Design: Molecular analysis correlated with phenotype. Setting: Academic medical center. Patient(s): A total of 168 IHH/KS patients as well as unrelated control subjects were studied for NELF mutations. Intervention(s): NELF coding regions/splice junctions were subjected to polymerase chain reaction (PCR)-based DNA sequencing. Eleven additional IHH/KS genes were sequenced in three patients with NELF mutations. Main Outcome Measure(s): Mutations were confirmed by sorting intolerant from tolerant, reverse-transcription (RT)-PCR, and Western blot analysis. Result(s): Three novel NELF mutations absent in 372 ethnically matched control subjects were identified in 3/168 (1.8%) IHH/KS patients. One IHH patient had compound heterozygous NELF mutations (c.629-21G>C and c.629-23C>G), and he did not have mutations in 11 other known IHH/KS genes. Two unrelated KS patients had heterozygous NELF mutations and mutation in a second gene: NELF/KAL1 (c.757G>A; p.Ala253Thr of NELF and c.488-490delGTT; p.Cys163del of KAL1) and NELF/TACR3 (c.1160-13C>T of NELF and c.824G>A; p.Trp275X of TACR3). In vitro evidence of these NELF mutations included reduced protein expression and splicing defects. Conclusion(s): Our findings suggest that NELF is associated with normosmic IHH and KS, either singly or in combination with a mutation in another gene.

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