The 2'-5' RNA Ligase of Escherichia coli: Purification, Cloning, and Genomic Disruption

An RNA ligase previously detected in extracts of Escherichia coli is capable of joining Saccharomyces cerevisiae tRNA splicing intermediates in the absence of ATP to form a 2-5 phosphodiester linkage (Greer, C., Javor, B., and Abelson, J. (1983) Cell 33, 899-906). This enzyme specifically ligates tRNA half-molecules containing nucleoside base modifications and shows a preference among different tRNA species. In order to investigate the function of this enzyme in RNA metabolism, the ligase was purified to homogeneity from E. coli lysate utilizing chromatographic techniques and separation of proteins by SDS-polyacrylamide gel electrophoresis. A single polypeptide of approximately 20 kilodaltons exhibited RNA ligase activity. The amino terminus of this protein was sequenced, and the open reading frame (ORF) encoding it was identified by a data base search. This ORF, which encodes a novel protein with a predicted molecular mass of 19.9 kDa, was amplified from E. coli genomic DNA and cloned. ORFs coding for highly similar proteins were detected in Methanococcus jannaschii and Bacillus stearothermophilus. The chromosomal gene encoding RNA ligase in E. coli was disrupted, abolishing ligase activity in cell lysates. Cells lacking ligase activity grew normally under laboratory conditions. However, moderate overexpression of the ligase protein led to slower growth rates and a temperature-sensitive phenotype in both wild-type and RNA ligase knockout strains. The RNA ligase reaction was studied in vitro using purified enzyme and was found to be reversible, indicating that this enzyme may perform cleavage or ligation in vivo

Multiple Worship Services and Church Growth

Approximately half of the 355,000 Protestant churches in the U.S. and Canada should consider adding a new style worship service to their weekly schedule of activities, regardless of the number of services they present offer. Of the churches that do begin a new service, eight out of ten will experience a measurable increase in 1) total worship attendance, 2) total giving, and 3) number of Christian conversions

Bye Bye Rocking Chair

Senior adults in most churches have more available time … give more financially (one study indicated seven times more) than younger members … have years of valuable experience working in the church … don’t go “church shopping,” nor do they often move their residence … their work quality is high, and church loyalty solid

Bye Bye Rocking Chair

Senior adults in most churches have more available time … give more financially (one study indicated seven times more) than younger members … have years of valuable experience working in the church … don’t go “church shopping,” nor do they often move their residence … their work quality is high, and church loyalty solid

Characteristics of People Who Live Long & Love It!

For centuries, laughter and positive emotions have been known to contribute to people’s health, healing, and happiness. Scripture records that “a cheerful heart is good medicine.” So senior adults — or anyone else who desires to live long and love it — will want to keep a twinkle in their eye and a merry heart

Analysis of TRIP expression in different types of skin tumor

TRAF-interacting protein (TRIP) is a ubiquitously expressed nucleolar E3 ubiquitin ligase. Ubiquitination of proteins is a post-translational modification, which decides on the cellular fate of the protein. TRIP in vivo substrate has not been yet identified. However, TRIP has been shown to play an important role in cellular proliferation, especially in keratinocytes. TRIP was found to be up-regulated in basal cell carcinoma (BCC) at the mRNA level. This prompted us to elucidate its role in skin proliferative diseases such as cancer by analyzing its expression in BCCs at protein level and in squamous cell carcinoma (SCC) at mRNA and protein level. To that purpose, we performed a real-time PCR (qPCR) analysis followed by an immunohistochemistry (IHC) on formalin-fixed, paraffin-embedded (FFPE) biopsies. The real-time PCR was performed on 12 RNA samples of which 6 were extracted from SCC biopsies and 6 from normal human skin. The results were statistically insignificant. Further analyses are needed on new RNA samples. The IHC assay was performed on 20 biopsies from BCCs, 21 biopsies from SCCs and on 5 tissues from normal human skin. The results obtained showed an extensive expression of TRIP in keratinocytes nuclei. Due to various limitations related to the technique and to doubts about preservation of the antigens in the tissues from normal human skin, we could not highlight a clear difference in TRIP expression between the different tissues. In conclusion, further analyses are needed on new RNA samples (qPCR) and on better preserved FFPE tissues from normal skin (IHC) to assess TRIP relative expression in BCCs and SCCs versus normal human skin

Learning to Love — At Any Age

What is it? It is not one of God’s attributes. It is the sum total of all God’s attributes. It is the reason Christ died on the cross for the sins of the world