Expression of heterogeneous nuclear ribonucleoprotein A2/B1 changes with critical stages of mammalian lung development

被引:46
作者
Montuenga, LM
Zhou, J
Avis, I
Vos, M
Martinez, A
Cuttitta, F
Treston, AM
Sunday, M
Mulshine, JL
机构
[1] NCI, Intervent Sect, CCBD, NIH,Med Branch, Bethesda, MD 20892 USA
[2] Univ Navarra, Dept Histol & Pathol, E-31080 Pamplona, Spain
[3] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
关键词
D O I
10.1165/ajrcmb.19.4.3185
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
Recent reports have demostrated a link between expression of members of the family of heterogeneous nuclear ribonucleoproteins (hnRNPs) and cancer. Overexpression of hnRNP A2/B1 correlated with the eventual development of lung cancer in three different clinical cohorts. We have studied the expression of hnRNP A2/B1 messenger RNA (mRNA) and protein during mammalian development. The expression of hnRNP A2/B1 mRNA and protein are parallel but change dynamically during critical periods in mouse pulmonary development. hnRNP A2/B1 is first detected in the lung in the early pseudoglandular period, peaks at the beginning of the canalicular period, and remains high during the saccular (alveolar) period. In mouse and rat, hnRNP A2/B1 expression is first evident in the earliest lung buds. As lung development progresses, the cuboidal epithelial cells of the distal primitive alveoli show high levels of the ribonucleoprotein, which is almost undetectable in the proximal conducting airways. The expression of hnRNP A2/B1 is restricted in mature lung. Similar dynamic pattern of expression through lung development was also found in rat and human lung. Upregulated expression of hnRNP A2/B1 at critical periods of lung development was comparable to the level of expression found in lung cancers and preneoplastic lesions and is consistent with hnRNP A2/B1 overexpression playing an oncodevelopmental role.
引用
收藏
页码:554 / 562
页数:9
相关论文
共 34 条
[1]   HUMAN HNRNP PROTEIN-A1 GENE-EXPRESSION - STRUCTURAL AND FUNCTIONAL-CHARACTERIZATION OF THE PROMOTER [J].
BIAMONTI, G ;
BASSI, MT ;
CARTEGNI, L ;
MECHTA, F ;
BUVOLI, M ;
COBIANCHI, F ;
RIVA, S .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 230 (01) :77-89
[2]   HUMAN IMPRINTED GENES AS ONCODEVELOPMENTAL MARKERS [J].
BIRAN, H ;
ARIEL, I ;
DEGROOT, N ;
SHANI, A ;
HOCHBERG, A .
TUMOR BIOLOGY, 1994, 15 (03) :123-134
[3]  
BOSSER R, 1995, MOL CELL BIOL, V15, P661
[4]   BOMBESIN-LIKE PEPTIDES CAN FUNCTION AS AUTOCRINE GROWTH-FACTORS IN HUMAN SMALL-CELL LUNG-CANCER [J].
CUTTITTA, F ;
CARNEY, DN ;
MULSHINE, J ;
MOODY, TW ;
FEDORKO, J ;
FISCHLER, A ;
MINNA, JD .
NATURE, 1985, 316 (6031) :823-826
[5]   HNRNP PROTEINS AND THE BIOGENESIS OF MESSENGER-RNA [J].
DREYFUSS, G ;
MATUNIS, MJ ;
PINOLROMA, S ;
BURD, CG .
ANNUAL REVIEW OF BIOCHEMISTRY, 1993, 62 :289-321
[6]  
FISHMAN WH, 1995, TUMOR BIOL, V16, P394, DOI 10.1159/000217956
[7]   RNA-dependent phosphorylation of a nuclear RNA binding protein [J].
Fung, PA ;
Labrecque, R ;
Pederson, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (04) :1064-1068
[8]   3 NEW MEMBERS OF THE RNP PROTEIN FAMILY IN XENOPUS [J].
GOOD, PJ ;
REBBERT, ML ;
DAWID, IB .
NUCLEIC ACIDS RESEARCH, 1993, 21 (04) :999-1006
[9]   NUCLEAR PROTEINS THAT BIND THE PREMESSENGER RNA 3' SPLICE-SITE SEQUENCE R(UUAG/G) AND THE HUMAN TELOMERIC DNA-SEQUENCE D(TTAGGG)N [J].
ISHIKAWA, F ;
MATUNIS, MJ ;
DREYFUSS, G ;
CECH, TR .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (07) :4301-4310
[10]  
ITAI S, 1990, CANCER RES, V50, P7603