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151.
O. Hedberg U. Karlsson E. Kelbessa O. Makunga G. Petterson M. Tadesse R. Västilä O. Wennberg 《Nordic Journal of Botany》1984,4(3):351-355
Detailed studies of comprehensive herbarium material confirmed that the afroalpine Cerastium adnivale Chiov. is too indistinctly delimited from the earlier described C. octandrum Hochst. ex A. Rich, to be given more than varietal rank. The restricted distribution of var. adnivale on only some of the high mountains harbouring C. octandrum s. lat. as well as results of experimental cultivation show that the reduced pubescence of the former cannot be due to environmental influence alone but must result from genetic differences. The derivation of var. adnivale from C. octandrum s. lat. is discussed. 相似文献
152.
153.
Mahalakshmi Krishnamurthy Serkalem Tadesse Katharina Rothmaier Peter L. Graumann 《Nucleic acids research》2010,38(2):455-466
Bacillus subtilis and most Gram positive bacteria possess four SMC like proteins: SMC, SbcC, RecN and the product of the yhaN gene, termed SbcE. SbcE is most similar to SbcC but contains a unique central domain. We show that SbcE plays a role during transformation in competent cells and in DNA double-strand break (DSB) repair. The phenotypes were strongly exacerbated by the additional deletion of recN or of sbcC, suggesting that all three proteins act upstream of RecA and provide distinct avenues for presynapsis. SbcE accumulated at the cell poles in competent cells, and localized as a discrete focus on the nucleoids in 10% of growing cells. This number moderately increased after treatment with DNA damaging agents and in the absence of RecN or of SbcC. Damage-induced foci of SbcE arose early after induction of DNA damage and rarely colocalized with the replication machinery. Our work shows that SMC-like proteins in B. subtilis play roles at different subcellular sites during DNA repair. SbcC operates at breaks occurring at the replication machinery, whereas RecN and SbcE function mainly, but not exclusively, at DSBs arising elsewhere on the chromosome. In agreement with this idea, we found that RecN-YFP damage-induced assemblies also arise in the absence of ongoing replication. 相似文献