This paper summarized the possible physiological mechanism by which anthocyanins strengthen the tolerance of plants to drought. Drought stress can in-duce plant cel s to synthesize and accumulate anthocyanins. The pho...This paper summarized the possible physiological mechanism by which anthocyanins strengthen the tolerance of plants to drought. Drought stress can in-duce plant cel s to synthesize and accumulate anthocyanins. The photochemical properties, subcel ular accumulation sites and spatial distributions in plant organs and tissues of anthocyanins determine their function of strengthening plant tolerance, which is realized by three possible physiological mechanisms： （1） anthocyanins and their chelated metal ions can optimize the osmoregulation ability of the plant cel s by directly acting as the osmoregulation substances of the cel s, （2） anthocyanins with suitable spatial locations can reduce the photoinhibition of the plants under drought stresses, （3） anthocyanins can effectively maintain and improve the active oxygen-scavenging capacity of the plant cel s under drought conditions. Therein, that the anthocyanins enhance the antioxidant capacity of the plant cel s under drought stresses is probably the main reason for the anthocyanins to strengthen the drought tolerance of plants. This review could provide a reference for the mechanism re-search of the drought resistance and the breeding of the drought-resistant cultivars for the plants holding the ability to synthesize and accumulate anthocyanins.展开更多
Chromosomal DNA replication is one of the central biological events occurring inside cells. Due to its large size, the replica-tion of genomic DNA in eukaryotes initiates at hundreds to tens of thousands of sites call...Chromosomal DNA replication is one of the central biological events occurring inside cells. Due to its large size, the replica-tion of genomic DNA in eukaryotes initiates at hundreds to tens of thousands of sites called DNA origins so that the replication could be completed in a limited time. Further, eukaryotic DNA replication is sophisticatedly regulated, and this regulation guarantees that each origin fires once per S phase and each segment of DNA gets duplication also once per cell cycle. The first step of replication initiation is the assembly of pre-replication complex （pre-RC）. Since 1973, four proteins, Cdc6/Cdcl8, MCM, ORC and Cdtl, have been extensively studied and proved to be pre-RC components. Recently, a novel pre-RC compo- nent called Sapl/Girdin was identified. Sapl/Girdin is required for loading Cdcl8/Cdc6 to origins for pre-RC assembly in the fission yeast and human cells, respectively. At the transition of G1 to S phase, pre-RC is activated by the two kinases, cy- clin-dependent kinase （CDK） and Dbf4-dependent kinase （DDK）, and subsequently, RPA, primase-polct, PCNA, topoisomer-ase, Cdc45, polδ and pole are recruited to DNA origins for creating two bi-directional replication forks and initiating DNA replication. As replication forks move along chromatin DNA, they frequently stall due to the presence of a great number of replication barriers on chromatin DNA, such as secondary DNA structures, protein/DNA complexes, DNA lesions, gene tran-scription. Stalled forks must require checkpoint regulation for their stabilization. Otherwise, stalled forks will collapse, which results in incomplete DNA replication and genomic instability. This short review gives a concise introduction regarding the current understanding of replication initiation and replication fork stabilization.展开更多
The fundamental unit of rapid, physiological color change in vertebrates is the dermal chromato- phore unit. This unit, comprised of cellular associations between different chromatophore types, is relatively conserved...The fundamental unit of rapid, physiological color change in vertebrates is the dermal chromato- phore unit. This unit, comprised of cellular associations between different chromatophore types, is relatively conserved across the fish, amphibian, and reptilian species capable of physiological color change and numerous attempts have been made to understand the nature of the four major chro- matophore types （melanophores, erythrophores, xanthophores, and iridophores） and their bio- chemical regulation. In this review, we attempt to describe the current state of knowledge regard- ing what classifies a pigment cell as a dynamic chromatophore, the unique characteristics of each chromatophore type, and how different hormones, neurotransmitters, or other signals direct pig- ment reorganization in a variety of vertebrate taxa.展开更多
基金Supported by the National Natural Science Foundation of China(31060045,31260091)~~
文摘This paper summarized the possible physiological mechanism by which anthocyanins strengthen the tolerance of plants to drought. Drought stress can in-duce plant cel s to synthesize and accumulate anthocyanins. The photochemical properties, subcel ular accumulation sites and spatial distributions in plant organs and tissues of anthocyanins determine their function of strengthening plant tolerance, which is realized by three possible physiological mechanisms： （1） anthocyanins and their chelated metal ions can optimize the osmoregulation ability of the plant cel s by directly acting as the osmoregulation substances of the cel s, （2） anthocyanins with suitable spatial locations can reduce the photoinhibition of the plants under drought stresses, （3） anthocyanins can effectively maintain and improve the active oxygen-scavenging capacity of the plant cel s under drought conditions. Therein, that the anthocyanins enhance the antioxidant capacity of the plant cel s under drought stresses is probably the main reason for the anthocyanins to strengthen the drought tolerance of plants. This review could provide a reference for the mechanism re-search of the drought resistance and the breeding of the drought-resistant cultivars for the plants holding the ability to synthesize and accumulate anthocyanins.
文摘Chromosomal DNA replication is one of the central biological events occurring inside cells. Due to its large size, the replica-tion of genomic DNA in eukaryotes initiates at hundreds to tens of thousands of sites called DNA origins so that the replication could be completed in a limited time. Further, eukaryotic DNA replication is sophisticatedly regulated, and this regulation guarantees that each origin fires once per S phase and each segment of DNA gets duplication also once per cell cycle. The first step of replication initiation is the assembly of pre-replication complex （pre-RC）. Since 1973, four proteins, Cdc6/Cdcl8, MCM, ORC and Cdtl, have been extensively studied and proved to be pre-RC components. Recently, a novel pre-RC compo- nent called Sapl/Girdin was identified. Sapl/Girdin is required for loading Cdcl8/Cdc6 to origins for pre-RC assembly in the fission yeast and human cells, respectively. At the transition of G1 to S phase, pre-RC is activated by the two kinases, cy- clin-dependent kinase （CDK） and Dbf4-dependent kinase （DDK）, and subsequently, RPA, primase-polct, PCNA, topoisomer-ase, Cdc45, polδ and pole are recruited to DNA origins for creating two bi-directional replication forks and initiating DNA replication. As replication forks move along chromatin DNA, they frequently stall due to the presence of a great number of replication barriers on chromatin DNA, such as secondary DNA structures, protein/DNA complexes, DNA lesions, gene tran-scription. Stalled forks must require checkpoint regulation for their stabilization. Otherwise, stalled forks will collapse, which results in incomplete DNA replication and genomic instability. This short review gives a concise introduction regarding the current understanding of replication initiation and replication fork stabilization.
文摘The fundamental unit of rapid, physiological color change in vertebrates is the dermal chromato- phore unit. This unit, comprised of cellular associations between different chromatophore types, is relatively conserved across the fish, amphibian, and reptilian species capable of physiological color change and numerous attempts have been made to understand the nature of the four major chro- matophore types （melanophores, erythrophores, xanthophores, and iridophores） and their bio- chemical regulation. In this review, we attempt to describe the current state of knowledge regard- ing what classifies a pigment cell as a dynamic chromatophore, the unique characteristics of each chromatophore type, and how different hormones, neurotransmitters, or other signals direct pig- ment reorganization in a variety of vertebrate taxa.
