Expression of mPer1 and mPer2, two mammalian clock genes, in murine bone marrow

被引:40
作者
Chen, YG
Mantalaris, A
Bourne, P
Keng, P
Wu, JHD
机构
[1] Univ Rochester, Dept Chem Engn, Rochester, NY 14627 USA
[2] Univ Rochester, Dept Radiat Oncol, Rochester, NY 14627 USA
[3] Univ Rochester, Dept Pathol & Lab Med, Rochester, NY 14627 USA
基金
美国国家科学基金会; 美国国家航空航天局;
关键词
circadian rhythm; circadian clock; mPer1; mPer2; bone marrow; hematopoiesis; biological clock;
D O I
10.1006/bbrc.2000.3536
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
Although circadian variations in hematopoiesis have been well documented, the molecular mechanism of the circadian rhythms remains elusive. To determine if a clock system exists in bone marrow to mediate the circadian rhythms, we analyzed the expression of mPer1 and mPer2, both mouse homologues of the Drosophila period gene and known regulators of the clock system, in murine bone marrow by relative quantitative reverse transcriptase-polymerase chain reaction (RT-PCR), We demonstrated that both genes were expressed in bone marrow. Furthermore, the expression patterns of mPer1 and mPer2 in total bone marrow cells exhibited two peaks over a 24-h period. In contrast, the expression patterns of these two genes in the Gr-1-positive cells isolated from bone marrow mainly contributed to one of the two peaks. These results indicate that a clock system exists in bone marrow and suggest that the circadian rhythms in bone marrow are lineage- and/or differentiation stage-dependent. (C) 2000 Academic Press.
引用
收藏
页码:724 / 728
页数:5
相关论文
共 25 条
[1]  
AARDAL NP, 1984, EXP HEMATOL, V12, P61
[2]  
AARDAL NP, 1983, EXP HEMATOL, V11, P792
[3]  
Abrahamsen JF, 1997, EUR J HAEMATOL, V58, P333
[4]  
Abrahamsen JF, 1998, EUR J HAEMATOL, V60, P7
[5]   A differential response of two putative mammalian circadian regulators, mper1 and mper2, to light [J].
Albrecht, U ;
Sun, ZS ;
Eichele, G ;
Lee, CC .
CELL, 1997, 91 (07) :1055-1064
[6]   A serum shock induces circadian gene expression in mammalian tissue culture cells [J].
Balsalobre, A ;
Damiola, F ;
Schibler, U .
CELL, 1998, 93 (06) :929-937
[7]   Molecular bases for circadian clocks [J].
Dunlap, JC .
CELL, 1999, 96 (02) :271-290
[8]   Circadian oscillation of BMAL1, a partner of a mammalian clock gene clock, in rat suprachiasmatic nucleus [J].
Honma, S ;
Ikeda, M ;
Abe, H ;
Tanahashi, Y ;
Namihira, M ;
Honma, K ;
Nomura, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (01) :83-87
[9]   mCRY1 and mCRY2 are essential components of the negative limb of the circadian clock feedback loop [J].
Kume, K ;
Zylka, MJ ;
Sriram, S ;
Shearman, LP ;
Weaver, DR ;
Jin, XW ;
Maywood, ES ;
Hastings, MH ;
Reppert, SM .
CELL, 1999, 98 (02) :193-205
[10]  
LAERUM OD, 1995, EXP HEMATOL, V23, P1145