Genetic and cytological evidence that heterocyst patterning is regulated by inhibitor gradients that promote activator decay

被引:66
作者
Risser, Douglas D. [1 ]
Callahan, Sean M. [1 ]
机构
[1] Univ Hawaii, Dept Microbiol, Honolulu, HI 96822 USA
基金
美国国家科学基金会;
关键词
activator-inhibitor; Anabaena; development; ANABAENA SP PCC-7120; SP STRAIN PCC-7120; BACILLUS-SUBTILIS; DIFFERENTIATION; HETR; PATS; LOCALIZATION; EXPRESSION; PROTEASE;
D O I
10.1073/pnas.0909152106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The formation of a pattern of differentiated cells from a group of seemingly equivalent, undifferentiated cells is a central paradigm of developmental biology. Several species of filamentous cyanobacteria differentiate nitrogen-fixing heterocysts at regular intervals along unbranched filaments to form a periodic pattern of two distinct cell types. This patterning has been used to exemplify application of the activator-inhibitor model to periodic patterns in biology. The activator-inhibitor model proposes that activators and inhibitors of differentiation diffuse from source cells to form concentration gradients that in turn mediate patterning, but direct visualization of concentration gradients of activators and inhibitors has been difficult. Here we show that the periodic pattern of heterocysts produced by cyanobacteria relies on two inhibitors of heterocyst differentiation, PatS and HetN, in a manner consistent with the predictions of the activator-inhibitor model. Concentration gradients of the activator, HetR, were observed adjacent to heterocysts, the natural source of PatS and HetN, as well as adjacent to vegetative cells that were manipulated to overexpress a gene encoding either of the inhibitors. Gradients of HetR relied on posttranslational decay of HetR. Deletion of both patS and hetN genes prevented the formation of gradients of HetR, and a derivative of the inhibitors was shown to promote decay of HetR in a concentration-dependent manner. Our results provide strong support for application of the activator-inhibitor model to heterocyst patterning and, more generally, the formation of periodic patterns in biological systems.
引用
收藏
页码:19884 / 19888
页数:5
相关论文
共 24 条
[1]   SPATIAL EXPRESSION AND AUTOREGULATION OF HETR, A GENE INVOLVED IN THE CONTROL OF HETEROCYST DEVELOPMENT IN ANABAENA [J].
BLACK, TA ;
CAI, YP ;
WOLK, CP .
MOLECULAR MICROBIOLOGY, 1993, 9 (01) :77-84
[2]   Inactivation of patS and hetN causes lethal levels of heterocyst differentiation in the filamentous cyanobacterium Anabaena sp PCC 7120 [J].
Borthakur, PB ;
Orozco, CC ;
Young-Robbins, SS ;
Haselkorn, R ;
Callahan, SM .
MOLECULAR MICROBIOLOGY, 2005, 57 (01) :111-123
[3]   Expression of the Anabaena hetR gene from a copper-regulated promoter leads to heterocyst differentiation under repressing conditions [J].
Buikema, WJ ;
Haselkorn, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) :2729-2734
[4]   CHARACTERIZATION OF A GENE CONTROLLING HETEROCYST DIFFERENTIATION IN THE CYANOBACTERIUM ANABAENA-7120 [J].
BUIKEMA, WJ ;
HASELKORN, R .
GENES & DEVELOPMENT, 1991, 5 (02) :321-330
[5]   The role of HetN in maintenance of the heterocyst pattern in Anabaena sp PCC 7120 [J].
Callahan, SM ;
Buikema, WJ .
MOLECULAR MICROBIOLOGY, 2001, 40 (04) :941-950
[6]  
ELHAI J, 1988, METHOD ENZYMOL, V167, P747
[7]   THEORY OF BIOLOGICAL PATTERN FORMATION [J].
GIERER, A ;
MEINHARDT, H .
KYBERNETIK, 1972, 12 (01) :30-39
[8]   Heterocyst development in Anabaena [J].
Golden, JW ;
Yoon, HS .
CURRENT OPINION IN MICROBIOLOGY, 2003, 6 (06) :557-563
[9]   Molecular evidence for an activator-inhibitor mechanism in development of embryonic feather branching [J].
Harris, MP ;
Williamson, S ;
Fallon, JF ;
Meinhardt, H ;
Prum, RO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (33) :11734-11739
[10]   HetR homodimer is a DNA-binding protein required for heterocyst differentiation, and the DNA-binding activity is inhibited by PatS [J].
Huang, X ;
Dong, YQ ;
Zhao, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :4848-4853