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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8 Citations (Scopus)


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
Issue number8
Publication statusPublished - 2000

Bibliographical note

Funding Information:
We thank Sir Walter Bodmer and Dr Ian Tomlinson for helpful discussion and critical review of this manuscript. This work was supported in part by a grant from the Korea Science and Engineering Foundation (KOSEF) through the Cancer Research Center at Seoul National University (KOSEF-CRC-97-8).

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research


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