scholarly journals B urkholderia cenocepacia conditional growth mutant library created by random promoter replacement of essential genes

2013 ◽  
Vol 2 (2) ◽  
pp. 243-258 ◽  
Author(s):  
Ruhi A. M. Bloodworth ◽  
April S. Gislason ◽  
Silvia T. Cardona
BioTechniques ◽  
2018 ◽  
Vol 65 (3) ◽  
pp. 159-162
Author(s):  
Pauline Texier ◽  
Michèle Coddeville ◽  
Patricia Bordes ◽  
Pierre Genevaux

BIO-PROTOCOL ◽  
2021 ◽  
Vol 11 (5) ◽  
Author(s):  
Shuai Shao ◽  
Lifan Wei ◽  
Feng Xia ◽  
Yuanxing Zhang ◽  
Qiyao Wang

Author(s):  
M. Antonia Molina-Henares ◽  
Jesús de la Torre ◽  
Adela García-Salamanca ◽  
A. Jesús Molina-Henares ◽  
M. Carmen Herrera ◽  
...  

2018 ◽  
Author(s):  
Yuwei Zhang ◽  
Yang Tao ◽  
Huihui Ji ◽  
Wei Li ◽  
Xingli Guo ◽  
...  

Genetics ◽  
1988 ◽  
Vol 120 (4) ◽  
pp. 977-986
Author(s):  
K J Kemphues ◽  
M Kusch ◽  
N Wolf

Abstract We have analyzed a set of linkage group (LG) II maternal-effect lethal mutations in Caenorhabditis elegans isolated by a new screening procedure. Screens of 12,455 F1 progeny from mutagenized adults resulted in the recovery of 54 maternal-effect lethal mutations identifying 29 genes. Of the 54 mutations, 39 are strict maternal-effect mutations defining 17 genes. These 17 genes fall into two classes distinguished by frequency of mutation to strict maternal-effect lethality. The smaller class, comprised of four genes, mutated to strict maternal-effect lethality at a frequency close to 5 X 10(-4), a rate typical of essential genes in C. elegans. Two of these genes are expressed during oogenesis and required exclusively for embryogenesis (pure maternal genes), one appears to be required specifically for meiosis, and the fourth has a more complex pattern of expression. The other 13 genes were represented by only one or two strict maternal alleles each. Two of these are identical genes previously identified by nonmaternal embryonic lethal mutations. We interpret our results to mean that although many C. elegans genes can mutate to strict maternal-effect lethality, most genes mutate to that phenotype rarely. Pure maternal genes, however, are among a smaller class of genes that mutate to maternal-effect lethality at typical rates. If our interpretation is correct, we are near saturation for pure maternal genes in the region of LG II balanced by mnC1. We conclude that the number of pure maternal genes in C. elegans is small, being probably not much higher than 12.


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