Complete cDNA encoding a putative phospholipase C from transformed human lymphocytes.

FEBS Lett

Department of Biochemistry, Jichi Medical School, Tochigi-ken, Japan.

Published: December 1988

Phosphoinositide-specific phospholipase C (PLC) is a crucial enzyme in transmembrane signaling. A cDNA encoding the putative phospholipase C was cloned from human lymphocytes that were transformed by infection with Epstein-Barr virus. The deduced amino acid sequence of the cDNA accounted for 146.1 kDa of the molecular mass of the complete enzyme and showed 50.2% sequence similarity to bovine brain PLC. This cDNA contained regions, the sequences of which were similar to those of some tyrosine kinase-related oncogene products. Northern blotting demonstrated that the mRNA for this PLC is expressed in human promyelocytic leukemia cells (HL-60). Since the other cloned cDNAs for PLCs could not hybridize with the RNA from this cell, it is strongly suggested that the gene obtained here encodes an additional isozyme of PLC in blood cells.

Download full-text PDF

Source
http://dx.doi.org/10.1016/0014-5793(88)80979-7DOI Listing

Publication Analysis

Top Keywords

cdna encoding
8
encoding putative
8
putative phospholipase
8
human lymphocytes
8
complete cdna
4
phospholipase transformed
4
transformed human
4
lymphocytes phosphoinositide-specific
4
phosphoinositide-specific phospholipase
4
plc
4

Similar Publications

Background: Immune checkpoint inhibitors have revolutionized cancer therapy, but many patients fail to respond or develop resistance, often due to reduced T cell activity. Costimulation via 4-1BB has emerged as a promising approach to enhance the effector function of antigen-primed T cells. Bispecific T cell-engaging (TCE) antibodies are an effective way to provide tumor-specific T cell receptor-mediated signaling to tumor-infiltrating lymphocytes.

View Article and Find Full Text PDF

The tardigrade Hypsibius exemplaris is an emerging model organism renowned for its ability to survive environmental extremes. To explore the molecular mechanisms and genetic basis of such extremotolerance, many studies rely on RNA-sequencing (RNA-seq), which can be performed on populations ranging from large cohorts to individual animals. Reverse transcription polymerase chain reaction (RT-PCR) and RNA interference (RNAi) are subsequently used to confirm RNA-seq findings and assess the genetic requirements for candidate genes, respectively.

View Article and Find Full Text PDF

Genetically Encoded Nucleic Acid Nanostructures for Biological Applications.

Chembiochem

January 2025

National Center for Nanoscience and Technology, CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, No.11 BeiYiTiao, ZhongGuanCun, 100190, Beijing, CHINA.

Nucleic acid, as a carrier of genetic information, has been widely employed as a building block for the construction of versatile nanostructures with pre-designed sizes and shapes through complementary base pairing. With excellent programmability, addressability, and biocompatibility, nucleic acid nanostructures are extensively applied in biomedical researches, such as bio-imaging, bio-sensing, and drug delivery. Notably, the original gene-encoding capability of the nucleic acids themselves has been utilized in these structurally well-defined nanostructures.

View Article and Find Full Text PDF

is an interferon-stimulated gene (ISG) that plays an important role in the congenital antiviral immunity of vertebrates. In this study, the common carp () gene is characterized, and we determine whether it has the ability to inhibit spring viremia of carp virus (SVCV) replication in EPC cells. The results showed that the full-length cDNA of the gene was 1044 bp and it encoded 348 amino acids.

View Article and Find Full Text PDF

Intraspecific variation and functional study of VERL polymorphism in Pacific abalone (Haliotis discus hannai Ino) and giant abalone (H. gigantea Gmelin).

Int J Biol Macromol

January 2025

State Key Laboratory of Mariculture Breeding, College of Ocean and Earth Sciences, Xiamen University, Xiamen 361102, China; Fujian Key Laboratory of Genetics and Breeding of Marine Organisms, College of Ocean and Earth Sciences, Xiamen University, Xiamen 361102, China. Electronic address:

Article Synopsis
  • Sperm and eggs have specific proteins called gamete recognition proteins (GRPs) that influence their compatibility in fertilization, and this study focuses on the VERL receptor in two abalone species.
  • The full-length VERL sequences were found to be different in Pacific abalone (11,373 bp) and giant abalone (9,405 bp), with variations in their amino acid compositions and repeats.
  • Notably, the study discovered a relationship between VERL genotypes and mating preferences in giant abalone, highlighting amino acid diversity's role in fertilization and providing insights for improving abalone breeding practices.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!