Altered cell-type proportioning in Dictyostelium lacking adenosine monophosphate deaminase

被引:9
作者
Chae, SC [1 ]
Fuller, D [1 ]
Loomis, WF [1 ]
机构
[1] Univ Calif San Diego, Ctr Mol Genet, Div Biol, La Jolla, CA 92093 USA
关键词
prespore cells; prestalk cells; AMP; IMP; purine metabolites;
D O I
10.1006/dbio.2001.0491
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The proportions of prespore and prestalk cells in Dictyostelium discoideum are regulated so that they are size invariant and can adjust when the ratio is perturbed. We have found that disruption of the gene amdA that encodes AMP deaminase results in a significantly increased proportion of prestalk cells. Strains lacking AMP deaminase form short, thick stalks and glassy sori with less than 5% the normal number of spores. The levels of prestalk-specific mRNAs in amdA- cells are more than twice as high as those in wild-type strains and prespore-specific mRNAs are reduced. Using an ecmA::lacZ construct to mark prestalk cells, we found that amdA- null slugs have twice the normal number of prestalk cells. The number of cells expressing an ecmO::lacZ construct was not affected by toss of AmdA, indicating that the mutation results in an increase in PST-A prestalk cells rather than PST-O cells. This alteration in cell-type proportioning is a cell-autonomous consequence of the loss of AMP deaminase since mutant cells developed together with wild-type cells still produced excess prestalk cells and wild-type cells carrying the ecmA::lacZ construct :formed normal numbers of prestalk cells when developed together with an equal number of amdA- mutant cells. (C) 2001 Elsevier Science.
引用
收藏
页码:183 / 194
页数:12
相关论文
共 53 条
[1]   ISOLATION OF DICTYOSTELIUM-DISCOIDEUM CYTOKINESIS MUTANTS BY RESTRICTION ENZYME-MEDIATED INTEGRATION OF THE BLASTICIDIN-S RESISTANCE MARKER [J].
ADACHI, H ;
HASEBE, T ;
YOSHINAGA, K ;
OHTA, T ;
SUTOH, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 205 (03) :1808-1814
[2]  
BAUSCHJURKEN MT, 1992, J BIOL CHEM, V267, P22407
[3]   PURINE NUCLEOTIDE CYCLE - PATHWAY FOR AMMONIA PRODUCTION IN RAT-KIDNEY [J].
BOGUSKY, RT ;
LOWENSTEIN, LM ;
LOWENSTEIN, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1976, 58 (02) :326-335
[4]   MITOTIC ACTIVITY IN RELATION TO DIFFERENTIATION IN THE SLIME MOLD DICTYOSTELIUM DISCOIDEUM [J].
BONNER, JT ;
FRASCELLA, EB .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1952, 121 (03) :561-571
[5]  
CHAPMAN AG, 1973, J BIOL CHEM, V248, P8309
[6]   A novel, putative MEK kinase controls developmental timing and spatial patterning in Dictyostelium and is regulated by ubiquitin-mediated protein degradation [J].
Chung, CY ;
Reddy, TBK ;
Zhou, KM ;
Firtel, RA .
GENES & DEVELOPMENT, 1998, 12 (22) :3564-3578
[7]   A ubiquitin-conjugating enzyme is essential for developmental transitions in Dictyostelium [J].
Clark, A ;
Nomura, A ;
Mohanty, S ;
Firtel, RA .
MOLECULAR BIOLOGY OF THE CELL, 1997, 8 (10) :1989-2002
[8]  
COFFEE CJ, 1977, J BIOL CHEM, V252, P1606
[9]   The role of apoptosis in the regulation of hematopoietic stem cells:: Overexpression of BCL-2 increases both their number and repopulation potential [J].
Domen, J ;
Cheshier, SH ;
Weissman, IL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (02) :253-263
[10]  
EARLY AE, 1993, DEVELOPMENT, V118, P353