ABSTRACT
The incidence of chromosomal abnormalities and cancer risk correlates well with the radiation dose after exposure to moderate- to high-dose ionizing radiation. However, the biological effects and health risks at less than 100 mGy, e.g., from computed tomography (CT) have not been ascertained. To investigate the biological effects of low-dose exposure from a CT procedure, we examined chromosomal aberrations, dicentric and ring chromosomes (dic+ring), in peripheral blood lymphocytes (PBLs), using FISH assays with telomere and centromere PNA probes. In 60 non-cancer patients exposed to CT scans, the numbers of dicentric and ring chromosomes were significantly increased with individual variation. The individual variations in the increment of dicentric and ring chromosomes after CT procedures were confirmed using PNA-FISH analysis of PBLs from 15 healthy volunteers after in vitro low-dose exposure using a 137Cs radiation device. These findings strongly suggest that appropriate medical use of low-dose radiation should consider individual differences in radiation sensitivity.
Subject(s)
Chromosome Aberrations , Lymphocytes/ultrastructure , Tomography, X-Ray Computed/methods , Adult , Aged , Cells, Cultured , Centromere , Cesium Radioisotopes , Female , Heart/diagnostic imaging , Humans , In Situ Hybridization, Fluorescence , Liver/diagnostic imaging , Male , Middle Aged , Peptide Nucleic Acids/chemistry , Radiation Dosage , TelomereABSTRACT
In sexual reproduction, proper communication and cooperation between male and female organs and tissues are essential for male and female gametes to unite. In flowering plants, female sporophytic tissues and gametophytes direct a male pollen tube toward an egg apparatus, which consists of an egg cell and two synergid cells. The cell-cell communication between the pollen tube and the egg apparatus makes the tip of pollen tube rupture to release the sperm cell. To detect male factors involved in this communication, we screened mutants of receptor-like kinases expressed in pollen tubes and characterized ANXUR1 (ANX1) and ANXUR2 (ANX2) genes. Here we report that pollen tubes of anx1/anx2 mutants ruptured before arriving at the egg apparatus, suggesting that ANX1 and ANX2 are male factors controlling pollen tube behavior by directing rupture at proper timing. Furthermore, ANX1 and ANX2 were the most closely related paralogs of a female factor, FERONIA/SIRENE, controlling pollen tube behavior expressed in synergid cells. Our findings show that the coordinated behaviors of female and male reproductive apparatuses are regulated by these sister genes, whose duplication might play a role in the evolution of the fertilization system in flowering plants.
Subject(s)
Arabidopsis Proteins/genetics , Arabidopsis/genetics , Cell Communication/physiology , Fertilization/physiology , Protein Kinases/genetics , Arabidopsis/physiology , Arabidopsis Proteins/metabolism , Cell Communication/genetics , Crosses, Genetic , Genotype , Immunohistochemistry , Mutation/genetics , Pollen Tube/genetics , Pollen Tube/physiology , Protein Kinases/metabolism , Reverse Transcriptase Polymerase Chain ReactionABSTRACT
The intracellular distribution of organelles plays a pivotal role in the maintenance and adaptation of a wide spectrum of cellular activities in plants. Chloroplasts are a special type of organelle able to photosynthesize, capturing light energy to fix atmospheric CO2. Consequently, the intracellular positioning of chloroplasts is crucial for plant growth and development. Knowledge of the photoreceptors and cellular apparatus responsible for chloroplast movement has gradually accumulated over time, yet recent advances have allowed improved understanding. In this article, several aspects of research progress into the mechanisms for maintaining the specific intracellular distribution patterns of chloroplasts, namely, chloroplast anchoring, are summarized, together with a brief consideration of the future prospects of this subject. Our discussion covers developmental, physiological, ecophysiological, and recent cell biological research areas.
