Isolation and characterisation of a novel human gene (C9orf11) on chromosome 9p21, a region frequently deleted in human cancer
被引:6
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作者:
Ruiz, A
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机构:
Hosp Duran & Reynals, IRO, Med & Mol Genet Ctr, Barcelona 08907, Catalonia, SpainHosp Duran & Reynals, IRO, Med & Mol Genet Ctr, Barcelona 08907, Catalonia, Spain
Ruiz, A
[1
]
Pujana, MA
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Hosp Duran & Reynals, IRO, Med & Mol Genet Ctr, Barcelona 08907, Catalonia, SpainHosp Duran & Reynals, IRO, Med & Mol Genet Ctr, Barcelona 08907, Catalonia, Spain
Pujana, MA
[1
]
Estivill, X
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Hosp Duran & Reynals, IRO, Med & Mol Genet Ctr, Barcelona 08907, Catalonia, SpainHosp Duran & Reynals, IRO, Med & Mol Genet Ctr, Barcelona 08907, Catalonia, Spain
Estivill, X
[1
]
机构:
[1] Hosp Duran & Reynals, IRO, Med & Mol Genet Ctr, Barcelona 08907, Catalonia, Spain
cutaneous malignant melanoma;
9p21;
loss of heterozygosity;
C9orf11;
novel gene;
D O I:
10.1016/S0167-4781(00)00272-4
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The chromosome 9p21 region has been described to be frequently deleted in several neoplasias. The cyclin dependent kinase inhibitor 2A (CDKN2A or Pld) gene was cloned in this region and identified as a tumour suppressor gene. However, much evidence indicates the existence of another tumour suppressor gene located proximal to the CDKN2A gene, which could be involved in cutaneous malignant melanoma (CMM) initiation. In the present report we have further investigated this 9p21 chromosomal region and cloned and characterised a novel gene within it (C9orf11). This gene shares no similarities to any known gene or predicted protein representing a novel human gene. Nevertheless, a putative leucine zipper pattern is located at the C-terminal end of the predicted protein, suggesting that it could dimerise. C9orf11 encodes for a protein of 294 amino acids with a predicted molecular mass of 32.8 kDa. C9orf11 is organised in eight exons that encompass a region of approx. 13 kb. Expression analysis demonstrates that C9orf11 is highly expressed in testis, although minor expression was seen in other tissues. Mutations in the C9orf11 gene were not detected in CMM families that were negative for CDKN2A mutations. Two SNPs for the C9orf11 gene have been identified, which could be used in segregation or association studies for other disorders. (C) 2000 Elsevier Science B.V. All rights reserved.
机构:Univ Calif San Francisco, Dept Urol, Res Ctr 112F, San Francisco, CA 94121 USA
Perinchery, G
Bukurov, N
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机构:Univ Calif San Francisco, Dept Urol, Res Ctr 112F, San Francisco, CA 94121 USA
Bukurov, N
Nakajima, K
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机构:Univ Calif San Francisco, Dept Urol, Res Ctr 112F, San Francisco, CA 94121 USA
Nakajima, K
Chang, J
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机构:Univ Calif San Francisco, Dept Urol, Res Ctr 112F, San Francisco, CA 94121 USA
Chang, J
Li, LC
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机构:Univ Calif San Francisco, Dept Urol, Res Ctr 112F, San Francisco, CA 94121 USA
Li, LC
Dahiya, R
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机构:
Univ Calif San Francisco, Dept Urol, Res Ctr 112F, San Francisco, CA 94121 USAUniv Calif San Francisco, Dept Urol, Res Ctr 112F, San Francisco, CA 94121 USA