Background: Werner syndrome (WS) is an autosomal recessive disorder with many features of premature ageing. Cells derived from WS patients show genomic instability, aberrations in the S-phase and sensitivity to genotoxic agents. The gene responsible for WS (WRN) encodes a DNA helicase belonging to the RecQ helicase family. Although biochemical studies showed that the gene product of WRN (WRNp) interacts with proteins that participate in DNA metabolism, its precise biological function remains unclear.
The current unpredictable climate changes are causing frequent and severe droughts. Such circumstances emphasize the need to understand the response of plants to drought stress, especially in rice, one of the most important grain crops. Knowledge of the drought stress response components is especially important in plant roots, the major organ for the absorption of water and nutrients from the soil. Thus, this article reviews the root response to drought stress in rice. It is presented to provide readers with information of use for their own research and breeding program for tolerance to drought stress in rice.
Cytosine methylation in the genome of Drosophila melanogaster has been elusive and controversial: Its location and function have not been established. We have used a novel and highly sensitive genomewide cytosine methylation assay to detect and map genome methylation in stage 5 Drosophila embryos. The methylation we observe with this method is highly localized and strand asymmetrical, limited to regions covering ∼1% of the genome, dynamic in early embryogenesis, and concentrated in specific 5-base sequence motifs that are CA- and CT-rich but depleted of guanine. Gene body methylation is associated with lower expression, and many genes containing methylated regions have developmental or transcriptional functions. The only known DNA methyltransferase in Drosophila is the DNMT2 homolog MT2, but lines deficient for MT2 retain genomic methylation, implying the presence of a novel methyltransferase. The association of methylation with a lower expression of specific developmental genes at stage 5 raises the possibility that it participates in controlling gene expression during the maternal-zygotic transition.
Werner's syndrome (WS) 1 is a rare autosomal recessive disorder characterized by premature aging and an early onset of age-related diseases including arteriosclerosis, malignant neoplasms, melituria, and cataract (1). Somatic cells derived from WS patients show chromosome instability, a shorter life span in in vitro culture, and accelerated telomere shortening (2, 3). WS cells have subtle defects in DNA replication, resulting in a reduced frequency of firing of replication origins (4). In addition, a large number of reports have shown that many cellular events including DNA repair, transcription, and apoptosis are affected in WS cells (5-7). The gene responsible for WS encodes a protein (WRN) that is a member of the RecQ family of DNA helicases (8). Most of the WS mutations that have been identified are nonsense or frameshift mutations, resulting in the truncation of WRN (9, 10). The clinical features and cellular phenotypes of most WS patients seem to be due to an absolute lack of WRN in the nucleus because the nuclear localization signal of WRN resides in its C-terminal end (11).The RecQ family includes Escherichia coli RecQ, S. cerevisiae Sgs1, Shizosaccharomyces pombe Rqh1, and five human RecQ helicases, namely DNA helicase Q1/RecQL (RecQL1), WRN, Bloom's syndrome gene product (BLM), Rhusmund-Thomson's syndrome gene product (RecQL4), and RecQL5 (12-19). Rhusmund-Thomson's syndrome also shows some features of the premature aging phenotype, and Bloom's syndrome is characterized by a predisposition to various malignant neoplasms. In S. cerevisiae, mutations in the SGS1 gene caused premature aging and hyper-recombination phenotypes (20, 21). The sgs1 mutants showed higher sensitivity to MMS and hydroxyurea (22)(23)(24)(25)37). Thus, sgs1 mutants exhibit some of the phenotypes of WS.WRN has been shown to have DNA helicase and exonuclease activity (26 -29). Recent studies (30 -32) have revealed that WRN interacts with replication protein A, PCNA, DNA topoisomerase I, and DNA polymerase ␦, indicating the involvement of WRN in some aspects of DNA replication. WRN also interacts with the p53 and Ku 70/86 heterodimer, suggesting that WRN is involved in apoptosis and the repair of DNA double strand breaks (7,(33)(34)(35). Despite these observations, it is not clear how the dysfunction of WRN is related to the observed phenotypes of WS cells. To obtain further insight into the process in which WRN is involved, we performed a two-hybrid screening using mouse WRN (mWRN) as bait and identified three interacting proteins: Ubc9, SUMO-1 (small ubiquitinrelated modifier-1), and a novel protein, WHIP (Werner Helicase Interacting Protein), which is conserved from E. coli to human (36). Here we report that mWRN physically interacts with mWHIP, and the yeast homologue of WRN, Sgs1, genetically interacts with yWHIP. EXPERIMENTAL PROCEDURESTwo-hybrid Assay-The yeast strains and plasmids for two-hybrid screening were described previously (36).
Background: Bloom's syndrome (BS) is an autosomal recessive disorder causing short stature, immunode®ciency, and an increased risk of cancer. Increased rates of sister chromatid exchange and chromosomal aberration have been observed in cells having defects in the BLM gene. Among ®ve kinds of human RecQ helicases cloned, the mutations in WRN and RecQL4 have been known as the causes of premature ageing. Little is, however, known about the function of BLM helicase in ageing.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.