High-mobility-group A1 (HMGA1) proteins down-regulate the expression of the recombination activating gene 2 (RAG2)

被引:13
作者
Battista, S
Fedele, M
Hoyos, JM
Pentimalli, F
Pierantoni, GM
Visone, R
De Martino, I
Croce, CM
Fusco, A
机构
[1] Univ Naples Federico II, Fac Med & Chirurg Napoli, Dipartimento Biol & Patol Cellulare & Mol, CNR,Ist Endocrinol & Oncol Sperimentale, I-80131 Naples, Italy
[2] Thomas Jefferson Univ, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[3] CEINGE, NOGEC, I-80145 Naples, Italy
关键词
electrophoretic mobility-shift assay (EMSA); embryonic stem cell; high-mobility-group A1 (HMGA1); lymphopoiesis; MEF; recombination activating gene 2 (RAG2);
D O I
10.1042/BJ20041607
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
HMGA1 (high-mobility-group A1) proteins are architectural transcription factors that are found overexpressed in embryogenesis and malignant tumours. We have shown previously that they have a role in lymphopoiesis, since the loss of HMGA1 expression leads to an impairment of T-cell development and to an increase in B-cell population. Since RAGs (recombination activating genes) are key regulators of lymphoid differentiation, in the present study we investigate whether RAG2 expression is dependent on HMGA1 activity. We show that RAG2 gene expression is up-regulated in Hmgal-/- ES (embryonic stem) cells and EBs (embryoid bodies) as well as in yolk sacs and fibroblasts from Hmgal-/- mice, suggesting that HMGA1 proteins control RAG2 gene expression both in vitro and in vivo. We show that the effect of HMGA1 on RAG2 expression is direct, identify the responsible region in the RAG2 promoter and demonstrate binding to the promoter in vivo using chromatin immunoprecipitation. Since RAG2 is necessary for lymphoid cell development, our results suggest a novel mechanism by which HMGA1 might regulate lymphoid differentiation.
引用
收藏
页码:91 / 97
页数:7
相关论文
共 31 条
  • [1] ABE T, 1994, J IMMUNOL, V152, P5504
  • [2] Onset of natural killer cell lymphomas in transgenic mice carrying a truncated HMGI-C gene by the chronic stimulation of the IL-2 and IL-15 pathway
    Baldassarre, G
    Fedele, M
    Battista, S
    Vecchione, A
    Klein-Szanto, AJP
    Santoro, M
    Waldmann, TA
    Azimi, N
    Croce, CM
    Fusco, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (14) : 7970 - 7975
  • [3] BALDASSARRE G, 2005, IN PRESS ONCOGENE
  • [4] Balde JW, 2003, EME TEC ADV PACK, V1, P1
  • [5] Battista S, 1999, CANCER RES, V59, P4793
  • [6] Loss of Hmga1 gene function affects embryonic stem cell lymphohematopoietic differentiation
    Battista, S
    Pentimalli, F
    Baldassarre, G
    Fedele, M
    Fidanza, V
    Croce, CM
    Fusco, A
    [J]. FASEB JOURNAL, 2003, 17 (09) : 1496 - +
  • [7] CHIAPPETTA G, 1995, ONCOGENE, V10, P1307
  • [8] Role of the high mobility group A proteins in human lipomas
    Fedele, M
    Battista, S
    Manfioletti, G
    Croce, CM
    Giancotti, V
    Fusco, A
    [J]. CARCINOGENESIS, 2001, 22 (10) : 1583 - 1591
  • [9] Functional analysis of the human RAG 2 promoter
    Fong, IC
    Zarrin, AA
    Wu, GE
    Berinstein, NL
    [J]. MOLECULAR IMMUNOLOGY, 2000, 37 (07) : 391 - 402
  • [10] The rag proteins and V(D)J recombination: Complexes, ends, and transposition
    Fugmann, SD
    Lee, AI
    Shockett, PE
    Villey, IJ
    Schatz, DG
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 : 495 - 527