Project/Area Number |
06454609
|
Research Category |
Grant-in-Aid for General Scientific Research (B)
|
Allocation Type | Single-year Grants |
Research Field |
Human genetics
|
Research Institution | Nagasaki University |
Principal Investigator |
NIKAWA Norio Nagasaki University, School of Medicine Professor, 医学部, 教授 (00111170)
|
Co-Investigator(Kenkyū-buntansha) |
JINNO Yoshihiro Nagasaki University, School of Medicine Lecturer, 医学部, 講師 (20179097)
|
Project Period (FY) |
1994 – 1995
|
Project Status |
Completed (Fiscal Year 1995)
|
Budget Amount *help |
¥7,100,000 (Direct Cost: ¥7,100,000)
Fiscal Year 1995: ¥2,400,000 (Direct Cost: ¥2,400,000)
Fiscal Year 1994: ¥4,700,000 (Direct Cost: ¥4,700,000)
|
Keywords | Transient leukemia / Down syndrome / Breakpoint analysis / Positional cloning / Gene isolation / Chromosome inversion / Cosmid contig / Tumor-related gene / 遺伝子 / 位置的単離 / 染色体転座 / 転座切断点 / YAC / コンティグ / 一過性骨髄異常増殖症 / 切断点クローン / STS |
Research Abstract |
Transient abnormal myclopoiesis (TAM) is a leukemoid reaction occurring occasionally in Down syndrome (DS) newborn infants. It has been hypothesized that "disomic homozygosity" in 21-trisomic cells plays an important-role in the genesis of TAM,and the putative TAM gene was suggested to be mapped at a 21q11 region. We encountered a DS-associated TAM infant with a 47, XY,inv (21) (q11.1q22.13), +inv (21) (q11.1q22.13) karyotype. Based on another presumption that in this patient, the putative TAM gene is disrupted by the break, we tried to isolate a breakpoint DNA.FISH analysis with cosmid clones corresponding to various STS markers mapped at around 21q11.1-q11.2, we confirmed that the proximal breakpoint of the inv (21) was located between two STSs, G51E07 and D21S215, the latter locus being consistent to the previous tentative mapping. After construction of a cosmid contig encompassing between the 2 markers, we have isolated a cosmid clone corresponding to the proximal breakpoint of the inversion. This breakpoint was located nearby a previously identified duplicated-region that is homologous to the sequence at 21q22.1. The isolated cosmid clone is useful for analysis of other TAM patients and for a search for a transcript at or flanking the breakpoint.
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