scholarly journals Molecular Genetic Dissection of Spawning, Parentage, and Reproductive Tactics in a Population of Redbreast Sunfish, Lepomis auritus

Evolution ◽  
1998 ◽  
Vol 52 (6) ◽  
pp. 1802 ◽  
Author(s):  
J. Andrew DeWoody ◽  
Dean E. Fletcher ◽  
S. David Wilkins ◽  
William S. Nelson ◽  
John C. Avise
Evolution ◽  
1998 ◽  
Vol 52 (6) ◽  
pp. 1802-1810 ◽  
Author(s):  
J. Andrew DeWoody ◽  
Dean E. Fletcher ◽  
S. David Wilkins ◽  
William S. Nelson ◽  
John C. Avise

Author(s):  
Melissa Riachi ◽  
Satyamaanasa Polubothu ◽  
Paulina Stadnik ◽  
Hughes Connor ◽  
Sara Barberan Martin ◽  
...  

Genetics ◽  
1998 ◽  
Vol 148 (4) ◽  
pp. 1963-1972 ◽  
Author(s):  
Jian-Dong Huang ◽  
Valerie Mermall ◽  
Marjorie C Strobel ◽  
Liane B Russell ◽  
Mark S Mooseker ◽  
...  

AbstractWe used an RT-PCR-based sequencing approach to identify the mutations responsible for 17 viable dilute alleles, a mouse-coat-color locus encoding unconventional myosin-VA. Ten of the mutations mapped to the MyoVA tail and are reported here. These mutations represent the first extensive collection of tail mutations reported for any unconventional mammalian myosin. They identify sequences important for tail function and identify domains potentially involved in cargo binding and/or proper folding of the MyoVA tail. Our results also provide support for the notion that different myosin tail isoforms produced by alternative splicing encode important cell-type-specific functions.


2001 ◽  
Vol 178 (S41) ◽  
pp. s128-s133 ◽  
Author(s):  
Nick Craddock ◽  
Ian Jones

BackgroundA robust body of evidence from family, twin and adoption studies demonstrates the importance of genes in the pathogenesis of bipolar disorder. Recent advances in molecular genetics have made it possible to identify these susceptibility genes.AimsTo present an overview for clinical psychiatrists.MethodReview of current molecular genetics approaches and emerging findings.ResultsOccasional families may exist in which a single gene plays a major role in determining susceptibility, but the majority of bipolar disorder involves more complex genetic mechanisms such as the interaction of multiple genes and environmental factors. Molecular genetic positional and candidate gene approaches are being used for the genetic dissection of bipolar disorder. No gene has yet been identified but promising findings are emerging. Regions of interest include chromosomes 4p16, 12q23–q24, 16p13, 21q22, and Xq24–q26. Candidate gene association studies are in progress but no robust positive findings have yet emerged.ConclusionIt is almost certain that over the next few years the identification of bipolar susceptiblity genes will have a major impact on our understanding of disease pathophysiology. This is likely to lead to major improvements and treatment in patient care, but will also raise important ethical issues.


2018 ◽  
Author(s):  
Michelle C Stitzer ◽  
Jeffrey Ross-Ibarra

The process of domestication presents a tractable system for following evolutionary change, as selective pressures shift, resulting in adaptation to the new ecological niche of cultivation. Perhaps the most detailed understanding of this process comes from Zea mays, where morphological, genetic, and genomic studies have elucidated the ancestry and selection that transformed a wild plant, the teosinte Zea mays subsp. parviglumis, into the domesticated maize Zea mays subsp. mays. These studies have identified five major morphological differences that distinguish these two subspecies, and careful genetic dissection of these phenotypes has assisted in understanding the underlying molecular genetic changes. But maize domestication was a consequence of more than just five genes, and regions throughout the genome contribute to this change. Their effects are contingent on genetic background, and the interactions between alleles and genes that give rise to phenotypes. This includes dominance relationships, epistatic interactions, and pleiotropic constraint, as well as how these variants are connected in gene networks. Together, we review the role of gene interactions in generating the dramatic phenotypic evolution seen in the transition from teosinte to maize.


2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Jonathan T. Ting ◽  
Brian Kalmbach ◽  
Peter Chong ◽  
Rebecca de Frates ◽  
C. Dirk Keene ◽  
...  

1997 ◽  
Vol 10 (1) ◽  
pp. 59-68 ◽  
Author(s):  
Qunyi Jiang ◽  
Peter M. Gresshoff

The model legume Lotus japonicus was demonstrated to be amenable to classical and molecular genetic analysis, providing the basis for the genetic dissection of the plant processes underlying nodulation and nitrogen fixation. We have developed an efficient method for the sexual hybridization of L. japonicus and obtained F1 progeny derived from a cross of L. japonicus B-129-S9 Gifu × B-581 Funakura. Over half of the cross-pollinations resulted in fertile hybrid seed, which were confirmed morphologically and by single arbitrary primer DNA amplification polymorphisms using the DAF technique. Molecular and morphological markers segregated in true Mendelian fashion in a F2 population of 100 plants. Several DAF loci were linked using the MAPMAKER software to create the first molecular linkage groups of this model legume. The mapping population was advanced to generate a set of immortal recombinant inbred lines (F6; RILs), useful for sharing plant material fixed genetically at most genomic regions. Morphological loci for waved stem shape (Ssh), dark leaf color (Lco), and short flowering period (Fpe) were inherited as single dominant Mendelian loci. DAF markers were dominant and were detected between Gifu and Funakura at about one per primer, suggesting that the parents are closely related. One polymorphism (270G generated by single octomer primer 8.6m) was linked to a morphological locus controlling leaf coloration. The results demonstrate that (i) Lotus japonicus is amenable to diploid genetic analysis, (ii) morphological and molecular markers segregate in true diploid fashion, (iii) molecular polymorphisms can be obtained at a reasonable frequency between the related Gifu and Funakura lines, and iv) the possibility exists for map-based cloning, marker assisted selection and mapping of symbiotic mutations through a genetic and molecular map.


Author(s):  
Maria Fitzgerald

Patrick (Pat) Wall was a neurophysiologist and true pioneer in the science of pain. He discovered that the sensory information arising from receptors in our body, such as those for touch and heat, could be modified, or ‘gated’, in the spinal cord by other sensory inputs and also by information descending from the brain; this meant, as is now well recognized, that the final sensory experience is not necessarily predictable from the original pain-eliciting sensory input. He used this to explain the poor relationship between injury and pain, and to illustrate the fallacy of judging what someone ‘should’ be feeling from the sensory input alone. In 1969, together with his colleague, Ron Melzack, Pat proposed the ‘gate control theory of pain’ and the circuit diagram that summarized how central spinal cord circuits can modulate sensory inputs. Later on, he began to regret that ‘goddamned diagram’, which had come to dominate his life and work, but, like all great models, it paved the way for the future. Now, over 50 years after it was first published, molecular genetic dissection of dorsal horn neuronal circuitry has indisputably confirmed that sensory inputs are indeed ‘gated’ in the spinal cord dorsal horn. Through a career that started with a medical degree in Oxford, followed by almost 20 years at Yale and MIT in the USA, and continued at University College London, Pat Wall was a highly influential, critical, creative and original thinker who revolutionized our understanding of the relationship between injury and pain, and who also became a champion for all who suffered from chronic pain.


2001 ◽  
Vol 158 (4) ◽  
pp. 515-520 ◽  
Author(s):  
G.a.d. Galili ◽  
Guiliang Tang ◽  
Xiaohong Zhu ◽  
Hagai Karchi ◽  
Daphna Miron ◽  
...  

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