Properties of the promoter region of theT18 d (T13 c )Tla gene

The T18^d (formerlyT13 ^c) gene of BALB/c mice belongs to the category ofTla genes which is expressed by both thymocytes and TL⁺ T-cell leukemias. To elucidate the regulation of T18^d, different restriction fragments of the 5' flanking region between -457 and⁺ 146 were linked to the chloramphenicol acetyltransferase (CAT) gene and transfected into TL⁺ and TL- cells. By comparison of transiently expresssedCAT activity among cells transfected with differentCAT constructs, the results suggest that determination of TL⁺ vs TL phenotypes is located within the region -105 to - 33, and that an element essential to T18 d expression resides within the region - 33 to + 54. Putative DNA-binding factors characterizing particular cell types and displaying selective affinity for particular TI 8^d restriction fragments were identified by electrophoretic mobility shift assays with nuclear extracts (NEs). Two factors (or complexes) which bound specifically to the T18^d fragment-105 to - 33 were expressed preferentially in TL⁺ cells and thus may be involved in determining the tissue-selective expression of TI8^d. The close proximity of negative and positive cis-acting elements within the promoter region is consistent with regulation of T18^d gene expression by a variety of trans-acting factors whose production is attuned to development and differentiation. The data provided may serve as a guide to study the regulation of other categories of Tla genes that are normally silent in thymocytes but may become expressed by leukemia cells.     

A new role for Cdks in the DNA damage response

Comment on: Alvarez-Fernández M, et al. EMBO Rep 2010; 11:452-8.     

Nucleotide sequence of the BALB/c H-2T region gene,T3 d

The nucleotide sequence data reported in this paper have been submitted to the GenBank nucleotide sequence database and have been assigned the accession number M75875.     

Nucleotide sequence of the bacteriophage T5 DNA fragment which contains the gene for tRNAAsp

The nucleotide sequence of bacteriophage T5 tRNAAsp has been determined by conventional methods using thin-layer chromatography on cellulose for oligonucleotide fractionation. It exhibits several unusual features, such as (a) the displacement of the constant residues U-8, A-14 and R-15; (b) the presence of three G X U out of four base pairs in the D-stem. The gene for T5 tRNAAsp has been cloned in pBR 322 and sequenced. The analysis of the flanking regions shows the presence of two open reading frames on both sides of this gene. It has also been shown that the cloned gene is expressed in Escherichia coli, and RNase P is involved in the T5 tRNAAsp processing.     

The complete nucleotide sequence of the I-E alpha d immune response gene.

We have isolated and sequenced the complete murine I-E alpha immune response gene of the H-2db haplotype. The I-E alpha d gene consists of 5300 basepairs and is organized into five or possibly six exons that correspond to different domains of the alpha chain. The amino acid sequence deduced from the I-E alpha gene shows 75% homology to its human counterpart, the HLA-DR alpha chain. The absence of I-E antigen in H-2 mice is due to lack of E alpha chain synthesis. We show here that this defect is caused by a deletion in the 5' end of the I-E alpha b gene.     

Alternate costimulatory molecules in T cell activation: differential mechanisms for directing the immune response

T cells are required for an effective immune response against a wide range of pathogens and for the generation of immunological memory. T cell activation can be divided into two phases: an antigen-specific signal delivered through the T cell antigen receptor, and a costimulatory signal delivered through accessory molecules on the T cell surface. Following activation, T cells differentiate to acquire distinct effector functions depending on the costimulatory signal, cytokine environment, and the pathogen itself. Although CD28 has been identified as the dominant costimulatory molecule, several other molecules have been described as having a costimulatory function. This review will focus on recent evidence for the existence of alternate costimulatory molecules, and the differential roles they might play in the activation, development, and survival of T cells.