植物叶片在衰老期间膜结构变化研究进展

引起生物体的器官或某一部分最终走向死亡的变化即为衰老(senescence),所有高等植物在其生活史上的任何阶段,或在任何结构水平上,衰老均可发生。衰老作为植物生长发育中的重要事件,受到研究者们的极大关注。1908年minot首先对植物的衰老进行了研究,对植物器官衰老研究最多的是叶片和子叶,一般地,子叶的衰老与叶片的衰老没有本质的差异。     

植物Whirly蛋白调控叶片衰老的研究进展

植物衰老是植物细胞生长发育的最后一个阶段,其启动的早晚对植物生物量和品质的形成有很大影响。叶片衰老是植物衰老的主要形式,受到内外环境因素的诱导,并被多种转录因子介导的信号传导途径所调控。对叶片衰老调控机制的研究一直是植物衰老研究中的重点。Whirly蛋白作为一类广泛存于植物中的特异转录因子小家族,能与单链DNA分子结合,双定位于细胞器(线粒体或叶绿体)与细胞核中,在植物细胞核和细胞器中发挥多种功能,参与对植物叶片衰老的调控。本文概述了植物Whirly蛋白的结构和定位,重点阐述了Whirly蛋白的功能与细胞衰老关系及其对叶片衰老调节机理的研究进展等,并对未来的研究方向进行了展望。     

植物衰老期间生理生化变化的研究进展

植物衰老是受内外因素控制的细胞有序降解并最终导致死亡的过程,衰老期间会出现与正常生长阶段不同的生理生化变化。植物衰老引起的各种功能的下降极大地限制了作物产量潜力的发挥,种子贮存过程中的衰变、逆境条件下植株的早衰、果蔬采后贮藏衰老导致货架寿命的缩短等均会造成极大的经济损失。研究植物衰老的生理机制及其调控具有十分重要的意义。综述了有关植物衰老时生理生化变化方面的近期研究进展,以利于人们对植物衰老生理的更深入的了解。     

植物衰老中的编程性细胞死亡

本文通过对植物衰老和动植物中编程性细胞死亡(PCD)的研究,阐述了植物衰老中PCD存在的依据,澄清了植物衰老和PCD的关系,提出了植物衰老中可能的PCD发生途径,为调控植物衰老的遗传操作提供依据.     

植物衰老中的编程性细胞死亡

本文通过对植物衰老和动植物中编程性细胞死亡(PCD)的研究,阐述了植物衰老中PCD存在的依据,澄清了植物衰老和PCD的关系,提出了植物衰老中可能的PCD发生途径,为调控植物衰老的遗传操作提供依据。     

谈谈植物的衰老

植物的衰老是指一个器官或整个植株的生命功能衰退、最终导致自然死亡的一系列变化的过程。衰老和死亡是植物的必然终结,认识衰老的原因,设法推迟衰老的进程是可能的。例如,水稻、小麦、棉花和油菜等作物的生长后期,由于肥水条件不良,常出现不同程度的早衰现象,影响...     

不同制剂在月季切花保鲜中的效果研究

以月季为材料,通过各种微生物保鲜剂的保鲜,了解其保鲜效果,并观察衰老过程中微生物与植物材料自身的生理变化,以探讨衰老原因。     

表观遗传调控植物叶片衰老的研究进展

植物叶片衰老是一个非常重要的发育过程,涉及大分子的有序分解从而将营养物质从叶片转移到其他器官,对植物的生存和适应至关重要。叶片衰老主要受植物的发育调控,但同时也受内部和外部环境因素的影响,涉及高度复杂的基因调控网络和多层级的调控。近年来的研究表明表观遗传是调控植物叶片衰老的一种重要调控方式。该研究综述了植物叶片衰老过程中的表观遗传调控机制,包括组蛋白修饰、DNA甲基化、ATP依赖的染色质重塑和非编码RNA介导的调控,并对该领域今后的发展方向进行了展望。     

一氧化氮与植物成熟衰老的关系

植物体可以通过依赖于类似哺乳动物的一氧化氮合成酶或硝酸还原酶的酶促合成途径和非酶促合成途径产生一氧化氮。植物内源一氧化氮可以通过抑制乙烯的生物合成和调控环化核苷酸在植物组织中的水平,来延缓植物组织的成熟和衰老,延长果蔬等组织的货架期。     

4—PU和6—BA对萝卜离体子叶衰老的延缓和脂质过氧化的影响

自70年代在植物衰老研究中引入自由基假说后,国内外不少研究表明在叶片衰老过程中确有自由基的参与,并导致脂质过氧化。近年来,许多研究者在植物生长调节物质延缓或加速植物衰老作用机理的研究中也非常重视自由基的作用。Leopold和Kriedemann〔1〕指出激动素有“基于自身氧化的刹车作用”。Leshem等〔2〕和Dhindsa等〔3〕报告细胞分裂素在延缓植物衰老方面的作用与它能清除自由基、阻止自由基的形成有关。李伯林等〔4〕用燕麦叶片为材料,发现6BA和2,4D在植物体内可作为直接和间接的自由基清除剂而延缓植物的衰老。早在50年代中后期就有报…     

Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis

It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.     

The structure, reproduction and taxonomy of Vidalia and Osmundaria (Rhodophyta, Rhodomelaceae)

Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.     

New or rare chromosome counts in Artemisia L. (Asteraceae, Anthemideae) and related genera from Kazakhstan

Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.     

肝癌中HBV和HCV基因和抗原的分布及意义

采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细     

Selection with two alleles and complete dominance

For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.