Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients

K. A. Yoon, J. L. Ku, H. S. Choi, S. C. Heo, S. Y. Jeong, Y. J. Park, N. K. Kim, J. C. Kim, P. M. Jung, J. G. Park

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Abstract

Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by hamartomatous gastrointestinal polyps and mucocutaneous pigmentation, with an increased risk for various neoplasms, including gastrointestinal cancer. Recently, the PJS gene encoding the serine/threonine kinase STK11 (also named LKB1) was mapped to chromosome 19p13.3, and germline mutations were identified in PJS patients. We screened a total of ten Korean PJS patients (nine sporadic cases and one familial case including two patients) to investigate the germline mutations of the STK11 gene. By polymerase chain reaction-single-strand conformation polymorphism and DNA sequencing analysis, three kinds of mis-sense mutation and a frame-shift mutation were identified: codon 232 (TCC to CCC) in exon 5, codon 256 (GAA to GCA) in exon 6, codon 324 (CCG to CTG) in exon 8, and a guanine insertion at codon 342 resulting in a premature stop codon in exon 8. These mis-sense variants were not detected in 100 control DNA samples. Furthermore, we found an intronic mutation at the dinucleotide sequence of a splice-acceptor site: a one base substitution from AG to CG in intron 1, which may cause aberrant splicing. Most reported germline mutations of the STK11 gene in PJS patients were frame-shift or non-sense mutations resulting in truncated proteins. Together, these findings indicate that germline mis-sense mutations of the STK11 gene are found in PJS patients in addition to truncating mutations. The effects of these mutations on protein function require further examination. In summary, we found germline mutations of the STK11 gene in five out of ten Korean PJS patients. (C) 2000 Cancer Research Campaign.

Original languageEnglish
Pages (from-to)1403-1406
Number of pages4
JournalBritish journal of cancer
Volume82
Issue number8
Publication statusPublished - 2000 Apr 11

Fingerprint

Peutz-Jeghers Syndrome
Germ-Line Mutation
Codon
Mutation
Exons
Genes
RNA Splice Sites
Frameshift Mutation
Gastrointestinal Neoplasms
Nonsense Codon
Protein-Serine-Threonine Kinases
Pigmentation
Guanine
Polyps
DNA Sequence Analysis
Introns
Proteins
Chromosomes
Polymerase Chain Reaction
DNA

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

Cite this

Yoon, K. A., Ku, J. L., Choi, H. S., Heo, S. C., Jeong, S. Y., Park, Y. J., ... Park, J. G. (2000). Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients. British journal of cancer, 82(8), 1403-1406.
Yoon, K. A. ; Ku, J. L. ; Choi, H. S. ; Heo, S. C. ; Jeong, S. Y. ; Park, Y. J. ; Kim, N. K. ; Kim, J. C. ; Jung, P. M. ; Park, J. G. / Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients. In: British journal of cancer. 2000 ; Vol. 82, No. 8. pp. 1403-1406.
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abstract = "Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by hamartomatous gastrointestinal polyps and mucocutaneous pigmentation, with an increased risk for various neoplasms, including gastrointestinal cancer. Recently, the PJS gene encoding the serine/threonine kinase STK11 (also named LKB1) was mapped to chromosome 19p13.3, and germline mutations were identified in PJS patients. We screened a total of ten Korean PJS patients (nine sporadic cases and one familial case including two patients) to investigate the germline mutations of the STK11 gene. By polymerase chain reaction-single-strand conformation polymorphism and DNA sequencing analysis, three kinds of mis-sense mutation and a frame-shift mutation were identified: codon 232 (TCC to CCC) in exon 5, codon 256 (GAA to GCA) in exon 6, codon 324 (CCG to CTG) in exon 8, and a guanine insertion at codon 342 resulting in a premature stop codon in exon 8. These mis-sense variants were not detected in 100 control DNA samples. Furthermore, we found an intronic mutation at the dinucleotide sequence of a splice-acceptor site: a one base substitution from AG to CG in intron 1, which may cause aberrant splicing. Most reported germline mutations of the STK11 gene in PJS patients were frame-shift or non-sense mutations resulting in truncated proteins. Together, these findings indicate that germline mis-sense mutations of the STK11 gene are found in PJS patients in addition to truncating mutations. The effects of these mutations on protein function require further examination. In summary, we found germline mutations of the STK11 gene in five out of ten Korean PJS patients. (C) 2000 Cancer Research Campaign.",
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Yoon, KA, Ku, JL, Choi, HS, Heo, SC, Jeong, SY, Park, YJ, Kim, NK, Kim, JC, Jung, PM & Park, JG 2000, 'Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients', British journal of cancer, vol. 82, no. 8, pp. 1403-1406.

Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients. / Yoon, K. A.; Ku, J. L.; Choi, H. S.; Heo, S. C.; Jeong, S. Y.; Park, Y. J.; Kim, N. K.; Kim, J. C.; Jung, P. M.; Park, J. G.

In: British journal of cancer, Vol. 82, No. 8, 11.04.2000, p. 1403-1406.

Research output: Contribution to journalArticle

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T1 - Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients

AU - Yoon, K. A.

AU - Ku, J. L.

AU - Choi, H. S.

AU - Heo, S. C.

AU - Jeong, S. Y.

AU - Park, Y. J.

AU - Kim, N. K.

AU - Kim, J. C.

AU - Jung, P. M.

AU - Park, J. G.

PY - 2000/4/11

Y1 - 2000/4/11

N2 - Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by hamartomatous gastrointestinal polyps and mucocutaneous pigmentation, with an increased risk for various neoplasms, including gastrointestinal cancer. Recently, the PJS gene encoding the serine/threonine kinase STK11 (also named LKB1) was mapped to chromosome 19p13.3, and germline mutations were identified in PJS patients. We screened a total of ten Korean PJS patients (nine sporadic cases and one familial case including two patients) to investigate the germline mutations of the STK11 gene. By polymerase chain reaction-single-strand conformation polymorphism and DNA sequencing analysis, three kinds of mis-sense mutation and a frame-shift mutation were identified: codon 232 (TCC to CCC) in exon 5, codon 256 (GAA to GCA) in exon 6, codon 324 (CCG to CTG) in exon 8, and a guanine insertion at codon 342 resulting in a premature stop codon in exon 8. These mis-sense variants were not detected in 100 control DNA samples. Furthermore, we found an intronic mutation at the dinucleotide sequence of a splice-acceptor site: a one base substitution from AG to CG in intron 1, which may cause aberrant splicing. Most reported germline mutations of the STK11 gene in PJS patients were frame-shift or non-sense mutations resulting in truncated proteins. Together, these findings indicate that germline mis-sense mutations of the STK11 gene are found in PJS patients in addition to truncating mutations. The effects of these mutations on protein function require further examination. In summary, we found germline mutations of the STK11 gene in five out of ten Korean PJS patients. (C) 2000 Cancer Research Campaign.

AB - Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by hamartomatous gastrointestinal polyps and mucocutaneous pigmentation, with an increased risk for various neoplasms, including gastrointestinal cancer. Recently, the PJS gene encoding the serine/threonine kinase STK11 (also named LKB1) was mapped to chromosome 19p13.3, and germline mutations were identified in PJS patients. We screened a total of ten Korean PJS patients (nine sporadic cases and one familial case including two patients) to investigate the germline mutations of the STK11 gene. By polymerase chain reaction-single-strand conformation polymorphism and DNA sequencing analysis, three kinds of mis-sense mutation and a frame-shift mutation were identified: codon 232 (TCC to CCC) in exon 5, codon 256 (GAA to GCA) in exon 6, codon 324 (CCG to CTG) in exon 8, and a guanine insertion at codon 342 resulting in a premature stop codon in exon 8. These mis-sense variants were not detected in 100 control DNA samples. Furthermore, we found an intronic mutation at the dinucleotide sequence of a splice-acceptor site: a one base substitution from AG to CG in intron 1, which may cause aberrant splicing. Most reported germline mutations of the STK11 gene in PJS patients were frame-shift or non-sense mutations resulting in truncated proteins. Together, these findings indicate that germline mis-sense mutations of the STK11 gene are found in PJS patients in addition to truncating mutations. The effects of these mutations on protein function require further examination. In summary, we found germline mutations of the STK11 gene in five out of ten Korean PJS patients. (C) 2000 Cancer Research Campaign.

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Yoon KA, Ku JL, Choi HS, Heo SC, Jeong SY, Park YJ et al. Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients. British journal of cancer. 2000 Apr 11;82(8):1403-1406.