Molecular characterisation of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication

被引:0
|
作者
Hildegard Kehrer-Sawatzki
Günter Assum
Horst Hameister
机构
[1] Department of Human Genetics,
[2] University of Ulm,undefined
[3] Albert-Einstein-Allee 11,undefined
[4] 89081 Ulm,undefined
[5] Germany,undefined
来源
Human Genetics | 2002年 / 111卷
关键词
Gene Duplication; Molecular Characterisation; Flank Region; Hybridisation Signal; Metaphase Chromosome;
D O I
暂无
中图分类号
学科分类号
摘要
A tandem duplication of the NF1 gene in 17q11.2 has recently been detected by high-resolution fluorescence in situ hybridisation (FISH) on stretched chromosomes and DNA fibres. These findings suggest not only that, in the 17q11.2 region, the NF1 gene is surrounded by NF1 low-copy repeats on each side of the gene, but also that the NF1 gene and its directly flanking regions are duplicated structures. However, if the NF1 gene is duplicated at 17q11.2, this should be observed by FISH analysis on metaphase chromosomes of relevant translocation carriers with the probes originally used to identify the duplication, since hybridisation signals of some of the probes would be expected on both derivative chromosomes, the der(17) and the der(22). We have only been able to obtain signals on the one or the other derivative of a female translocation carrier. Therefore, our results do not support the hypothesis of a duplication of the NF1 gene and its immediately flanking regions at 17q11.2 as had been previously postulated. Rather, our findings suggest that there is one NF1 gene in the 17q11.2 region.
引用
收藏
页码:465 / 467
页数:2
相关论文
共 50 条
  • [1] Molecular characterisation of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication
    Kehrer-Sawatzhi, H
    Assum, G
    Hameister, H
    HUMAN GENETICS, 2002, 111 (4-5) : 465 - 467
  • [2] 46,XY,t(10;18;21)(q22;q11.2;q11.2)一例
    陈莉莎
    于月新
    邹朋书
    陈霞慧
    马明
    中华医学遗传学杂志, 2018, (03) : 396 - 396
  • [3] 22q11.2 SYNDROME DUE TO MATERNAL TRANSLOCATION t(18;22) (p11.2;q11.2)
    Nur, B. G.
    Cetin, Z.
    Clark, O. A.
    Mihci, E.
    Oygur, N.
    Karauzum, S. B.
    GENETIC COUNSELING, 2015, 26 (01): : 67 - 75
  • [4] First report of t(1;15)(q21;q11.2) and t(1;21)(q21;q11.2) anomalies in Burkitt Lymphoma
    Bozkurt, Sureyya
    Okay, Mufide
    Haznedaroglu, Celalettin Ibrahim
    KUWAIT MEDICAL JOURNAL, 2021, 53 (03): : 344 - 345
  • [5] A complex t(15;22;17)(q22;q11.2;q21) variant of APL
    Ak, Bilgesu
    Gungor, Ozge
    Karaca, Emin
    Durmaz, Burak
    Bozer, Denis S.
    Tobu, Mahmut
    Akin, Haluk
    CANCER GENETICS, 2024, 286 : 48 - 51
  • [6] 46,XX,t(8;13;21)(q11.2;q14;q11.2)一例
    刘秀英
    刘晓光
    朱继红
    陈芳
    中华医学遗传学杂志, 2014, (04) : 527 - 527
  • [7] Chronic myeloid leukemia with a rare variant BCR-ABL translocation: t(9;22;21)(q34;q11.2;q11.2)
    Takeuchi, Mai
    Katayama, Yoshio
    Okamura, Atsuo
    Yamamoto, Katsuya
    Shimoyama, Manabu
    Matsui, Toshimitsu
    CANCER GENETICS AND CYTOGENETICS, 2007, 179 (01) : 85 - 87
  • [8] Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome
    Goodman, BK
    Rutberg, J
    Lin, WW
    Pulver, AE
    Thomas, GH
    Geraghty, MT
    JOURNAL OF INHERITED METABOLIC DISEASE, 2000, 23 (08) : 847 - 848
  • [9] Medulloblastoma in a patient with a balanced t (5;22)(q35.1;q11.2) affecting the NF2 gene
    Roque, Lucia
    Faria, Claudia
    Nunes, Sofia
    Pimentel, Jose
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 415 - 415
  • [10] Molecular studies of an ependymoma-associated constitutional t(1;22)(p22;q11.2)
    Rhodes, CH
    Call, KM
    Budarf, ML
    Barnoski, BL
    Bell, CJ
    Emanuel, BS
    Bigner, SH
    Park, JP
    Mohandas, TK
    CYTOGENETICS AND CELL GENETICS, 1997, 78 (3-4): : 247 - 252