A NEW FAMILY OF HEPARIN BINDING GROWTH-DIFFERENTIATION FACTORS - DIFFERENTIAL EXPRESSION OF THE MIDKINE (MK) AND HB-GAM GENES DURING MOUSE DEVELOPMENT

被引:52
作者
NAKAMOTO, M
MATSUBARA, S
MIYAUCHI, T
OBAMA, H
OZAWA, M
MURAMATSU, T
机构
[1] Department of Biochemistry, Faculty of Medicine, Kagoshima University, Kagoshima, Kagoshima 890
关键词
D O I
10.1093/oxfordjournals.jbchem.a123903
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
MK (midkine) and HB-GAM (heparin-binding growth-associated molecule) constitute a new family of heparin-binding growth differentiation factors. The modes of expression of MK and HB-GAM during mouse development were quantitatively examined by mRNA hybridization. The following three distinct patterns of expression were observed in the brain/head region. On the 11th-13th days of gestation, MK was intensely, but HB-GAM relatively weakly expressed; on the 15th-19th days, both MK and HB-GAM expression became weaker; and in the neonatal period, HB-GAM was intensely expressed and MK expression increased slightly. The level of HB-GAM expression was lower than that of MK in the whole embryo on the 11th to 13th days of gestation. HB-GAM mRNA was detected in the kidney of newborn and young mice, where MK was more highly expressed. The identity of the weakly expressed MK and HB-GAM signals was confirmed by means of the polymerase chain reaction in the neonatal brain (MK), the head of 13-day embryos (HB-GAM), and the kidney of 7-day-old mice (HB-GAM). In conclusion, MK and HB-GAM are frequently co-expressed in the same cells and anatomic regions of the fetus or new born mouse, while their modes of expression differ.
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页码:346 / 349
页数:4
相关论文
共 32 条
[1]   THE HEPARIN-BINDING (FIBROBLAST) GROWTH-FACTOR FAMILY OF PROTEINS [J].
BURGESS, WH ;
MACIAG, T .
ANNUAL REVIEW OF BIOCHEMISTRY, 1989, 58 :575-606
[2]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[3]   MITOGENIC PROPERTIES OF A NEW ENDOTHELIAL-CELL GROWTH-FACTOR RELATED TO PLEIOTROPHIN [J].
COURTY, J ;
DAUCHEL, MC ;
CARUELLE, D ;
PERDERISET, M ;
BARRITAULT, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 180 (01) :145-151
[4]   CLONING AND EXPRESSION OF 2 DISTINCT HIGH-AFFINITY RECEPTORS CROSS-REACTING WITH ACIDIC AND BASIC FIBROBLAST GROWTH-FACTORS [J].
DIONNE, CA ;
CRUMLEY, G ;
BELLOT, F ;
KAPLOW, JM ;
SEARFOSS, G ;
RUTA, M ;
BURGESS, WH ;
JAYE, M ;
SCHLESSINGER, J .
EMBO JOURNAL, 1990, 9 (09) :2685-2692
[5]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[6]   DIDEOXY SEQUENCING METHOD USING DENATURED PLASMID TEMPLATES [J].
HATTORI, M ;
SAKAKI, Y .
ANALYTICAL BIOCHEMISTRY, 1986, 152 (02) :232-238
[7]  
HUANG RP, 1990, DEV GROWTH DIFFER, V32, P189
[8]  
Jacobson M., 2013, DEV NEUROBIOL
[9]   A RETINOIC ACID RESPONSIVE GENE MK FOUND IN THE TERATOCARCINOMA SYSTEM IS EXPRESSED IN SPATIALLY AND TEMPORALLY CONTROLLED MANNER DURING MOUSE EMBRYOGENESIS [J].
KADOMATSU, K ;
HUANG, RP ;
SUGANUMA, T ;
MURATA, F ;
MURAMATSU, T .
JOURNAL OF CELL BIOLOGY, 1990, 110 (03) :607-616
[10]   CDNA CLONING AND SEQUENCING OF A NEW GENE INTENSELY EXPRESSED IN EARLY DIFFERENTIATION STAGES OF EMBRYONAL CARCINOMA-CELLS AND IN MID-GESTATION PERIOD OF MOUSE EMBRYOGENESIS [J].
KADOMATSU, K ;
TOMOMURA, M ;
MURAMATSU, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 151 (03) :1312-1318