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51.
52.
^60Co—γ射线诱导的小麦T型雄性不育系育性恢复突变 总被引:5,自引:1,他引:4
用~(60)Co-γ射线诱导小麦T型雄性不育系T小偃4号A、T郑引1号A均获得了农艺性状优良、恢复力强的恢复系。育性恢复突变是涉及一个或少数几个位点核基因的显性突变。利用性状优良的T型不育系诱导育性恢复突变是选育恢复系和发掘恢复源的有效途径。 相似文献
53.
54.
Summary Microtubules tightly cross-linked into bundles are described in the sperm cells ofBrassica oleracea pollen tubes. The sperm cells are lobed and tailed and the microtubule bundles are often located in these parts of the cells. In the present paper we suggest that the cross-linked microtubule organization could determine an intertubular sliding, probably generating a motility system that propels the sperm cells through the tube.Abbreviations GC
generative cell
- Mfs
microfilaments
- Mts
microtubules
- SC
sperm cell
- VC
vegetative cell
- VN
vegetative nucleus 相似文献
55.
N. A. Dudareva S. G. Veprev A. V. Popovsky S. I. Maletsky I. P. Gileva R. I. Salganik 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1990,79(6):817-824
Summary Among the fertile sugar beet lines with nuclear sterility maintenance genes, rf, in a homozygous recessive state, sublines capable of reverting spontaneously at a high rate to sterility were identified. Of 24 related fertile sublines studied, 6 were found to spontaneously revert to sterility with a frequency of about 19%. Genetic analysis confirmed the cytoplasmic nature of spontaneously arising sterility. Reversion to sterility in these sublines was accompanied by alterations in the mitochondrial genome structure: loss of the autonomously replicating minicircle c (1.3 kb) and changes in the restriction patterns of high-molecular-weight mitochondrial DNA (mtDNA). Southern hybridixation analysis with cloned minicircle c as a probe revealed no integration of this DNA molecule into the main mitochondrial and nuclear genomes of the revertants. Comparative BamHI and EcoRI restriction analysis of the mtDNA from the sterile revertants and fertile parental subline showed that the spontaneous reversion is accompanied by extensive genomic rearrangement. Southern blot analysis with cloned -subunit of F1-ATPase (atpA) and cytochrome c oxidase subunit II (COX II) genes as probes indicated that the changes in mtDNA accompanying spontaneous reversion to sterility involved these regions. The mitochondrial genomes of the spontaneous revertants and the sterile analogue were shown to be identical. 相似文献
56.
The prokaryotic endosymbionts that became plastids and mitochondria contained genes destined for one of three fates. Genes
required for free-living existence were lost. Most genes useful to the symbiosis were transferred to the nucleus of the host.
Some genes, a small minority, were retained within the organelle. Here we suggest that a selective advantage of movement of
genes to the nucleus is decreased mutation: plastids and mitochondria have high volume-specific rates of redox reactions,
producing oxygen free radicals that chemically modify DNA. These mutations lead to synthesis of modified electron carriers
that in turn generate more mutagenic free radicals—the “vicious circle” theory of aging. Transfer of genes to the nucleus
is also advantageous in facilitating sexual recombination and DNA repair. For genes encoding certain key components of photosynthesis
and respiration, direct control of gene expression by redox state of electron carriers may be required to minimize free radical
production, providing a selective advantage of organelle location which outweighs that of location in the nucleus. A previous
proposal for transfer of genes to the nucleus is an economy of resources in having a single genome and a single apparatus
for gene expression, but this argument fails if any organellar gene is retained. A previous proposal for the retention of
genes within organelles is that certain proteins are organelle-encoded because they cannot be imported, but there is now evidence
against this view. Decreased free radical mutagenesis and increased sexual recombination upon transfer to the nucleus together
with redox control of gene expression in organelles may now account for the slightly different gene distributions among nuclei,
plastids, and mitochondria found in major eukaryote taxa. This analysis suggests a novel reason for uniparental inheritance
of organelles and the evolution of anisogametic sex, and may also account for the occurrence of nitrogen fixation in symbionts
rather than in nitrogen-fixing organelles.
Correspondence to: J.F. Allen 相似文献
57.
内源植物激素与光敏核不育水稻农垦58S育性的关系 总被引:22,自引:1,他引:21
采用气相色谱-质谱联用选择离子检测(GC-MS-SIM)技术,定性、定量分析了光敏核不育水稻农垦58S(Oryza sativa L. subsp. japonica)及对照品种“农垦58”在长(LD)、短(SD)日照处理下,不同发育时期顶端全展叶片中内源IAA、ABA 和生殖器官中内源IAA、ABA、GA1、GA4 的含量变化。实验结果表明:在LD 处理下,农垦58S雌雄蕊形成期的叶片和花粉母细胞形成期的幼穗中IAA 相继发生亏缺;农垦58S-LD花粉母细胞形成期、单核期和扬花期,生殖器官中内源ABA 均低于农垦58S-SD 的含量,“农垦58”则与此相反;扬花期不育花药中内源GA1 和GA4 含量剧减。据此认为:生殖器官中早期IAA 的亏损、ABA 含量剧减伴随着抗逆性能的减弱及GAS的不足共同导致了农垦58S的雄性败育 相似文献
58.
一个恢复力受单基因控制的水稻CMS育性回复突变体 总被引:3,自引:0,他引:3
利用 ̄(60)Co-γ射线对具有印尼水田谷细胞质的籼稻细胞质雄性不育系Ⅱ-32A干种子进行诱变处理,获得了一育性回复突变体T24。育性基因未纯合的突变体分离出可育株和完全不育株,比例为3∶1;其与Ⅱ-32A和珍汕97A测交,F1代分离出1∶1的可育株和不育株。育性稳定株系与Ⅱ-32A和珍汕97A杂交,F2分离成3∶1的可育株和不育株。表明其育性回复是由一对基因显性突变所致。这一突变体对不育系的育性恢复机制不同于明恢63、20964等恢复系,后者表现为两对显性恢复基因作用。未观察到T24与亲本Ⅱ-32A除育性以外的其他性状的差异,因而两者构成育性恢复基因的近等基因系。本文还对不育系育性回复类型和T24的理论意义与育种价值进行了讨论。 相似文献
59.
Paternal genome loss (PGL) during early embryogenesis is caused by two different genetic elements in the parasitoid wasp, Nasonia vitripennis. Paternal sex ratio (PSR) is a paternally inherited supernumerary chromosome that disrupts condensation of the paternal chromosomes by the first mitotic division of fertilized eggs. Bacteria belonging to the genus Wolbachia are present in Nasonia eggs and also disrupt paternal chromosome condensation in crosses between cytoplasmically incompatible strains. Cytoplasmic incompatibility Wolbachia are widespread in insects, whereas PSR is specific to this wasp. PGL results in production of male progeny in Nasonia due to haplodiploid sex determination. The cytological events associated with PGL induced by the PSR chromosome and by Wolbachia were compared by fluorescent light microscopy using the fluorochrome Hoescht 33258. Cytological examination of eggs fertilized with PSR-bearing sperm revealed that a dense paternal chromatin mass forms prior to the first metaphase. Quantification of chromatin by epifluorescence indicates that this mass does undergo replication along with the maternal chromatin prior to the first mitotic division but does not replicate during later mitotic cycles. Contrary to previous reports using other staining methods, the paternal chromatin mass remains condensed during interphase and persists over subsequent mitotic cycles, at least until formation of the syncytial blastoderm and cellularization, at which time it remains near the center of the egg with the yolk nuclei. Wolbachia-induced PGL shows several marked differences. Most notable is that the paternal chromatin mass is more diffuse and tends to be fragmented during the first mitotic division, with portions becoming associated with the daughter nuclei. Nuclei containing portions of the paternal chromatin mass appear to be delayed in subsequent mitotic divisions relative to nuclei free of paternal chromatin. Crosses combining incompatibility with PSR were cytologically similar to Wolbachia-induced PGL, although shearing of the paternal chromatin mass was reduced. Wolbachia may, therefore, block an earlier stage of paternal chromatin processing in the fertilized eggs than does PSR. © 1995 Wiley-Liss, Inc. 相似文献
60.
Hillard S. Kaplan Jane B. Lancaster Sara E. Johnson John A. Bock 《Human nature (Hawthorne, N.Y.)》1995,6(4):325-360
Our objective is to test an optimality model of human fertility that specifies the behavioral requirements for fitness maximization
in order (a) to determine whether current behavior does maximize fitness and, if not, (b) to use the specific nature of the behavioral deviations from fitness maximization towards the development of models of evolved
proximate mechanisms that may have maximized fitness in the past but lead to deviations under present conditions. To test
the model we use data from a representative sample of 7,107 men living in Albuquerque, New Mexico, between 1990 and 1993.
The model we test proposes that low fertility in modern settings maximizes number of grandchildren as a result of a trade-off
between parental fertility and next generation fertility. Results do not show the optimization, although the data do reveal
a trade-off between parental fertility and offspring education and income.
We propose that two characteristics of modern economies have led to a period of sustained fertility reduction and to a corresponding
lack of association between income and fertility. The first is the direct link between costs of investment and wage rates
due to the forces of supply and demand for labor in competitive economies. The second is the increasing emphasis on cumulative
knowledge, skills, and technologies in the production of resources. Together they produce historically novel conditions. These
two features of modern economies may interact with evolved psychological and physiological mechanisms governing fertility
and parental investment to produce behavior that maximizes the economic productivity of lineages at the expense of fitness.
If cognitive processes evolved to track diminishing returns to parental investment and if physiological processes evolved
to regulate fertility in response to nutritional state and patterns of breast feeding, we might expect non-adaptive responses
when returns from parental investment do not diminish until extremely high levels are reached. With high economic payoffs
from parental investment, people have begun to exercise cognitive regulation of fertility through contraception and family
planning practices. Those cognitive processes maynot have evolved to handle fitness trade-offs between fertility and parental investment.
A preliminary presentation of this data was published in R. I. M. Dunbar, ed.,Human Reproduction Decisions: Biological and Social Perspectives. New York: St. Martin’s Press, 1995. Support for the research project, “Male Fertility and Parenting in New Mexico,” began
with two seed grants from the University of New Mexico’s Biomedical Research Grants Program, 1988 and 1989, and one from the
University of New Mexico Research Allocations Committee, 1988. Further seed money as well as interim funding came from the
William T. Grant Foundation (#89130589 and #91130501). The major support for the project came from the National Science Foundation
from 1990 to 1993 (#BNS-9011723 and #DBS-911552). Both National Science Foundation grants included Research Experience for
Undergraduates supplements.
Hillard S. Kaplan is an Associate Professor of Anthropology at the University of New Mexico. His earlier research and publications
focused on food sharing, time allocation, parental investment, and reproductive strategies among Ache hunter-gatherers in
Paraguay, Machiguenga and Piro forager-horticulturalists in Peru, and villagers of several ethnicities in Botswana. New research
and theory concern fertility, parental investment, and mating strategies in developed and developing nations. This research
formulates a new theory of reproductive decision-making and the demographic transition, integrating human capital and parental
investment theory in a synthesis of economic and evolutionary approaches.
Jane B. Lancaster is a Professor of Anthropology at the University of New Mexico. Her research and publications are on human
reproductive biology and behavior, especially human parental investment; women’s reproductive biology of pregnancy, lactation,
and child-spacing; and male fertility and investment in children. Current research with Hillard S. Kaplan is on male life
history strategies among a large sample of men in New Mexico. She has coedited three books on human parental investment:School-Age Pregnancy and Parenthood (with B. Hamburg),Parenting across the Life Span (with J. Altmann, A. Rossi, and L. Sherrod), andOffspring Abuse and Neglect (with R. Gelles). She is scientific editor of a quarterly journal,Human Nature: An Interdisciplinary, Biosocial Perspective published by Aldine de Gruyter. She is also a council member of the newly formed Human Behavior and Evolution Society.
John A. Bock is Andrew W. Mellon Post-Doctoral Fellow in Epidemiology and Population Health at the National Centre for Epidemiology
and Population Health, The Australian National University. His research focuses on the allocation of parental investment and
the determinants of children’s activities, integrating aspects of economic and evolutionary theory. He has ongoing field research
with Bantu and Bushmen agro-pastoralists and forager-horticulturalists in the Okavango Delta, Botswana. He is also collaborating
with Lancaster and Kaplan on the determinants of progeny distribution and homosexuality among New Mexican men.
Sara E. Johnson is a Ph.D. candidate at the University of New Mexico. Her major research trajectory focuses on trade-offs
in life history characters. Her research experience includes participation in a study of variation in growth and development
among children in a multi-ethnic community in the Okavango Delta, Botswana, in addition to her dissertation work on individual
variation in growth and mortality among juvenile baboons. She is collaborating with Lancaster and Kaplan on the association
between survival and fertility among Albuquerque men. 相似文献