Mutations in four regulatory genes have interrelated effects on heterocyst maturation in Anabaena sp strain PCC 7120

被引:16
作者
Lechno-Yossef, Sigal
Fan, Qing
Ehira, Shigeki
Sato, Naoki
Wolk, C. Peter [1 ]
机构
[1] Michigan State Univ, DOE Plant Res Lab, E Lansing, MI 48824 USA
[2] Michigan State Univ, Dept Plant Biol, E Lansing, MI 48824 USA
[3] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, Tokyo, Japan
关键词
D O I
10.1128/JB.00974-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Regulatory genes hepK, hepN, henR, and hepS are required for heterocyst maturation in Anabaena sp. strain PCC 7120. They presumptively encode two histidine kinases, a response regulator, and a serine/threonine kinase, respectively. To identify relationships between those genes, we compared global patterns of gene expression, at 14 h after nitrogen step-down, in corresponding mutants and in the wild-type strain. Heterocyst envelopes of mutants affected in any of those genes lack a homogeneous, polysaccharide layer. Those of a henR mutant also lack a glycolipid layer. patA, which encodes a positive effector of heterocyst differentiation, was up-regulated in all mutants except the hepK mutant, suggesting that pat,4 expression may be inhibited by products related to heterocyst development. hepS and hepK were up-regulated if mutated and so appear to be negatively autoregulated. HepS and HenR regulated a common set of genes and so appear to belong to one regulatory system. Some nontranscriptional mechanism may account for the observation that henR mutants lack, and hepS mutants possess, a glycolipid layer, even though both mutations down-regulated genes involved in formation of the glycolipid layer. HepK and HepN also affected transcription of a common set of genes and therefore appear to share a regulatory pathway. However, the transcript abundance of other genes differed very significantly from expression in the wild-type strain in either the hepK or hepN mutant while differing very little from wild-type expression in the other of those two mutants. Therefore, hepK and hepN appear to participate also in separate pathways.
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页码:7387 / 7395
页数:9
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