Expression of IL-10 as a transgene inhibits murine mammary tumor growth and metastasis. Using differential display methodology, we sought genes whose expression was modulated by IL-10. We compared mRNA isolated from parental murine mammary 66.1 tumors, as well as tumors derived from neo r -transfect
Transposon 10 promoted deletions and inversions in the transfer genes of R100-1
β Scribed by Kehoe, M. A. ;Foster, T. J.
- Publisher
- Springer
- Year
- 1979
- Tongue
- English
- Weight
- 786 KB
- Volume
- 176
- Category
- Article
- ISSN
- 0026-8925
No coin nor oath required. For personal study only.
β¦ Synopsis
Spontaneous tetracycline-sensitive, transfer-deficient mutants of R100-1 were selected and analysed by genetic complementation tests and with the restriction endonuclease EcoR1. While some of the Tets Tra- mutants were caused by a single deletion event which removed the Tetr genes and extended into the neighbouring transfer genes, other mutants were the result of the deletion of the Tetr genes within Tn10 which was accompanied by an inversion of adjacent DNA sequences. A clustering of deletion and inversion endpoints occurred in the traA gene. Some of the transfer genes of R100-1 were assigned to EcoR1 fragments.
π SIMILAR VOLUMES
## Abstract ## Background Acidic fibroblast growth factor (FGFβ1) has been identified as a potent mitogen for vascular cells, inducing formation of mature blood vessels __in vitro__ and __in vivo__ and represents one of the most promising approaches for the treatment of ischemic cardiovascular dis
The effects of tetracycline on transfer of the conjugative, tetracycline-resistance transposon. Tn925, as well as the ability of the transposon to promote the transfer of chromosomal genes was examined in Enterococcus faecalis and Bacillus subtilis. To test for chromosomal transfer, multiply-marked
We identified a novel 12-bp deletion NT\_033927.7: g.5495364\_5495375del in the 5'-flanking region of the SERPINH1 gene that increases promoter activity. The 12-bp deletion is in linkage disequilibrium with the minor "T" allele of the -656 C/T SNP (NT\_033927.7(SERPINH1):g.5495402C>T) that reduces p
Background Gene therapy, and particularly gene restoration, is currently a great hope for non-curable hereditary retinal degeneration. Clinical applications require a gene transfer vector capable of accurately targeting particular cell types in the retina. To develop such a vector, we compared the e