• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

1997 Fiscal Year Final Research Report Summary

Cloning of disease-causing genes for the syndrome with congenital heart malformations

Research Project

Project/Area Number 08457231
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionKeio University

Principal Investigator

MINOSHIMA Shinsei  Keio University, School of Medicine, Assistant professor, 医学部・講師(現 助教授) (90181966)

Co-Investigator(Kenkyū-buntansha) SHIMIZU Nobuyoshi  Keio University, School of Medicine, Professor, 医学部, 教授 (50162706)
Project Period (FY) 1996 – 1997
Keywordscongenital heart malformations / cat eye syndrome / marker chromosome / region specific cosmid library / BAC library / BAC / cosmid contig / genomic sequencing / gene / exon prediction
Research Abstract

We have approached the disease-responsible genes for heart malformation in cat eye syndrome (CES) and obtained the following results.
(1) We have constructed BAC/cosmid contigs of the CES chromosomal region (CER ; 1.9 Mb in size). We used two DNA libraries, a CES region-specific cosmid library (9,200 clones ; redundancy, 10) from the flow-sorted marker chromosomes of a CES cell line CH91-157 and a BAC library (200,000 clones ; redundancy, 7.5) from human total DNA, both of which were established by ourselves. A number of known DNA markers, newly established STS's from cosmid clones, and YAC clones isolated with these DNA markers were used to screen the BAC and CES cosmid libraries, and as a result 1,740 cosmids and 116 BAC clones were isolated. The vectorette PCR method and fingerprinting have been applied to construct BAC/cosmid contigs. To date, 6 contigs consisting of 33 BAC and 43 cosmid clones have been constructed to cover >1.3 Mb region.
(2) Genomic sequencing of 4 BAC and 7 cosmid clones have almost been finished which covers 〜300 kb in CER. We have encountered a great difficulty to construct contigs and determine the sequence of this peri-centromeric region due to high contents of repetitive sequences and high homology with other chromosomes such as chromosome 14 and other heterochromatin-containing chromosomes.
(3) The DNA sequence is being analyzed by exon-prediction programs (GENSCAN, GRAIL) and homology search tools (BLAST, FASTA) followed by isolation of corresponding cDNA's.

  • Research Products

    (37 results)

All Other

All Publications (37 results)

  • [Publications] Footz, T.K.: "The gene for death agonist BID2 maps to the region of human 22q11.2 duplicated in cat eye syndrome chromosomes and to mouse chromosome 6"Genomics. 51. 472-475 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Matsuoka, R.: "Molecular and Clinical Study of 183 Patients with Conotruncal Anomaly Face Syndrome"Hum. Genet.. 103. 70-80 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Johnson, A.: "A 1.5-Mb contig within the cat eye syndrome critical region at human chromosome 22q11.2"Genomics. 57. 306-309 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Riazi, M.A.: "Identification of a putative regulatory subunit of a calcium-activated potassium channel in the dup (3q) syndrome region and a related sequence on 22q11.2"Genomics. 62. 90-94 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Dunham, I.: "The DNA sequence of human chromosome 22"Nature. 402. 489-495 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Minoshima, S.: "Eye disorder database "KMeyeDB""Human Mutation. 15. 95-98 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Minoshima, S.: "Keio Mutation Database "KMDB" for Human Disease Gene Mutations"Nucleic Acids Res.. 28. 364-368 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Riazi, M.A.: "The human homolog of insect-derived growth factor, CECR1, is candidate gene for features of cat eye syndrome"Genomics. 64. 277-285 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kawasaki, K.: "Propagation and maintenance of the 119 human immunoglobulin Vlambda genes and pseudogenes during evolution"J. Exp. Zool.. 288. 120-134 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 清水信義: "ヒトゲノムプロジェクトの最前線-ヒト22番染色体から学んだこと-"最新医学. 55(6). 1097-1188 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Minoshima, S.: "The KMDB/Mutation View : a mutation database for human disease genes"Nucleic Acids Res.. 29. 327-328 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Dawson, E.: "SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence"Genome Res.. 11. 170-178 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] International Human Genome Mapping Consortium: "A physical map of the human genome"Nature. 409. 934-941 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] International Human Genome Sequencing Consortium: "Initial sequencing and analysis of the human genome"Nature. 409. 860-921 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Luijten, M.: "Duplication and transposition of the NF1 pseudogene regions on chromosome 2,14 and 22"Hum. Genet.. 109. 109-116 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Footz, T.K.: "Analysis of the cat eye syndrome critical region in humans and the region at conserve synteny in mice : A search for candidate genes at or near the human chromosome 22 pericentromere"Genome Res.. 11. 1053-1070 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Sasaki, T.: "Molecular cloning of a member of the facilitative glucose transporter gene family GLUT11 (SLC2A11) and identification of transcirption variants"Biochem. Biophys. Res. Commun.. 289. 1218-1224 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Shiohama, A.: "Molecular cloning and expression analysis of a novel gene DGCR8 located in the DiGeorge syndrome chromosomal region"Biochem. Biophys. Res. Commun.. 304. 184-190 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Sasaki, T.: "Identification of eight members of the argonaute family in the human genome"Genomics. (in press).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Footz, T. K., Birren, B., Minoshima, S., Asakawa, S., Shimizu, N., Riazi, M. A. and McDermid, H. E.: "The gene for death agonist BID2 maps to the region of human 22q11.2 duplicated in cat eye syndrome chromosomes and to mouse chromosome 6"Genomics. 51. 472-475 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Matsuoka, R., Kimura, M., Scambler, P.J., Morrow, B.E., Imamura, S., Minoshima, S., Shimizu, N., Yamagishi, H., Joh-o, K., Watabane, S., Oyama, K., Saji, T., Ando, M., Takao, A. and Momma, K.: "Molecular and Clinical Study of 183 Patients with Conotruncal Anomaly Face Syndrome"Hum. Genet. 103. 70-80 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Johnson, A., Minoshima, S., Asakawa, S., Shimizu, N., Shizuya, H., Roe, B. A., McDermid, H. E.: "A 1.5-Mb contig within the cat eye syndrome critical region at human chromosome 22q11.2"Genomics. 57. 306-309 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Riazi, M. A., Brinkman-Mills, P., Johnson, A., Naylor, S. L., Minoshima, S., Shimizu, N., Baldini, A., and McDermid, H. E.: "Identification of a putative regulatory subunit of a calcium-activated potassium channel in the dup(3q) syndrome region and a related sequence on 22q11.2"Genomics. 62. 90-94 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Dunham, I., Shimizu, N., Roe, B. A., Chissoe, S. et al.: "The DNA sequence of human chromosome 22"Nature.. 402. 489-495 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Minoshima, S., Mitsuyama, S., Ohno, S., Kawamura, T. and Shimizu, N.: "Eye disorder database "KMeyeDB""Human Mutation. 15. 95-98 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Minoshima, S., Mitsuyama, S., Ohno, S., Kawamura, T. and Shimizu, N.: "Keio Mutation Database "KMDB" for Human Disease Gene Mutations"Nucleic Acids Res.. 28. 364-368 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Riazi, M.A., Brinkman-Mills, P., Nguyen, T., Pan, H., Phan, S., Ying, F., Roe, B.A., Tochigi, J., Shimizu, Y., Minoshima, S., Shimizu, N., Buchwald, M., McDermid, H.E.: "The human homolog of insect-derived growth factor, CECR1, is a candidate gene for features of cat eye syndrome"Genomics.. 64. 277-285 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kawasaki, K., Minoshima, S., Shimizu, N.: "Propagation and maintenance of the 119 human immunoglobulin V lambda genes and pseudogenes during evolution"J. Exp. Zool.. 288. 120-134 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Minoshima, S., Mitsuyama, S., Ohtsubo, M., Kawamura, T., Ito, S., Shibamoto, S., Ito, F., Shimizu, N.: "The KMDB/MutationView : a mutation database for human disease genes"Nucleic Acids Res.. 29. 327-328 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Dawson, E., Chen, Y., Hunt, S., Smink, L.J., Hunt, A., Rice, K., Livingston, S., Bumpstead, S., Bruskiewich, R., Sham, P., Ganske, R., Adams, M., Kawasaki, K., Shimizu, N., Minoshima, S., Roe, B., Bentley, D., Dunham, I. A.: "SNP resource for human chromosome 22 : extracting dense clusters of SNPs from the genomic sequence"Genome Res.. 11. 170-178 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] "International Human Genome Mapping Consortium : A physical map of the human genome"Nature. 409. 934-941 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] "International Human Genome Sequencing Consortium : Initial sequencing and analysis of the human genome"Nature. 409. 860-921 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Luijten, M., Redeker, S., Minoshima, S., Shimizu, N., Westerveld, A., Hulsebos, T. J.: "Duplication and transposition of the NF1 pseudogene regions on chromosome 2,14 and 22"Hum. Genet.. 109. 109-116 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Footz, T. K., Brinkman-Mills, P., Banting, G. S., Maier, S. A., Riazi, M. A., Bridgland, L., Hu, S., Birren, B., Minoshima, S., Shimizu, N., Pan, HQ, Nguyen, T., Fang, F., Fu, Y., Ray, L., Wu, H., ShauU, S., Phan, S., Yao, Z,, Chen, F., Huan, A., Hu, P., Wang, Q., Loh, P., Qi, S., Roe, B. A., McDermid, H. E.: "Analysis of the cat eye syndrome critical region in humans and the region of conserved synteny in mice : A search for candidate genes at or near the human chromosome 22 pericentromere"Genome Res.. 11. 1053-1070 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Sasaki, T., Minoshima, S., Shiohama, A., Shintani, A., Shimizu, A., Asakawa, S., Kawasaki, K. and Shimizu, N.: "Molecular cloning of a member of the facilitative glucose transporter gene family GLUT11 (SLC2A11) and identification of transcirption variants"Biochem. Biophys. Res. Commun.. 289. 1218-1224 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shiohama, A., Sasaki, T., Noda, S., Minoshima, S. and Shimizu, N.: "Molecular cloning and expression analysis of a novel gene DGCR8 located in the DiGeorge syndrome chromosomal region"Biochem. Biophys. Res. Commun.. 304. 184-190 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Sasaki, T., Shiohama, A., Minoshima, S. and Shimizu, N.: "Identification of eight members of the argonaute family in the human genome"Genomics. in press.

    • Description
      「研究成果報告書概要(欧文)」より

URL: 

Published: 2004-04-14  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi