scholarly journals A single gene with pleiotropic effects accounts for the Scottish endemic taxon Athyrium distentifolium var. flexile

2001 ◽  
Vol 152 (3) ◽  
pp. 491-500 ◽  
Author(s):  
H. S. McHaffie ◽  
C. J. Legg ◽  
R. A. Ennos
EvoDevo ◽  
2014 ◽  
Vol 5 (1) ◽  
pp. 5 ◽  
Author(s):  
Margaret G Mills ◽  
Anna K Greenwood ◽  
Catherine L Peichel

Genetics ◽  
1988 ◽  
Vol 119 (3) ◽  
pp. 705-710
Author(s):  
L D Gottlieb ◽  
D de Vienne

Abstract We examined, by two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), near-isogenic lines of the r-gene in pea (Pisum sativum) which determines round (RR) vs. wrinkled (rr) seed. The study was undertaken to assess the number of protein changes resulting from a single gene substitution as a means of quantifying pleiotropic effects. A total of 636 to 770 resolvable polypeptides were identical in all respects between RR and rr for roots, shoots, leaflets, stipules, young ovaries, and young embryos. A single difference between the lines became evident about 21-23 days after anthesis in the embryos. Mature seeds of the two lines showed 62 spot differences in addition to differences in four clusters of spots, representing about 10% of the total number of spots visible on the gels. The protein differences are presumably involved in the many known physiological differences of the two seed types. 2-D PAGE analyses of near-isogenic lines are likely to be valuable in a number of quantitative and developmental genetic contexts.


2016 ◽  
Vol 72 (10) ◽  
pp. 1910-1925 ◽  
Author(s):  
Nathalie Colbach ◽  
Bruno Chauvel ◽  
Henri Darmency ◽  
Christophe Délye ◽  
Valérie Le Corre

The number of observable “characters” in an organism is infinite. The number of genes which control development is limited. It follows that many, perhaps most, genes must not affect only one organ or character, but several at a time. Their effect is manifold, and the term “pleiotropism” has been coined to cover this diversity of actions of a single gene. The question arises: How does a gene produce its “pleiotropic” effects ? An agent X which produces the effects a and b can do so in three different ways. X may produce a and b directly, but in two independent and different ways ( X → a → b ). Or X may produce a and b directly, but in essentially the same way ( X —→ a → b ). Or X may produce one of its effects ( a ) directly, and this primary product in turn conditions the other effect ( b ). This is a causal chain, ( X → a → b or X → b → a ),one effect being subordinated to the other and following it in time. The primary effect may still be notice­ able when the secondary effect has developed; then we observe “pleiotropism” in space, whereas otherwise we observe it only in time. If more than two effects are conditioned by X , combinations of these three funda­mental ways of causation may occur.


2020 ◽  
Vol 477 (16) ◽  
pp. 3091-3104 ◽  
Author(s):  
Luciana E. Giono ◽  
Alberto R. Kornblihtt

Gene expression is an intricately regulated process that is at the basis of cell differentiation, the maintenance of cell identity and the cellular responses to environmental changes. Alternative splicing, the process by which multiple functionally distinct transcripts are generated from a single gene, is one of the main mechanisms that contribute to expand the coding capacity of genomes and help explain the level of complexity achieved by higher organisms. Eukaryotic transcription is subject to multiple layers of regulation both intrinsic — such as promoter structure — and dynamic, allowing the cell to respond to internal and external signals. Similarly, alternative splicing choices are affected by all of these aspects, mainly through the regulation of transcription elongation, making it a regulatory knob on a par with the regulation of gene expression levels. This review aims to recapitulate some of the history and stepping-stones that led to the paradigms held today about transcription and splicing regulation, with major focus on transcription elongation and its effect on alternative splicing.


Diabetes ◽  
2018 ◽  
Vol 67 (Supplement 1) ◽  
pp. 2312-PUB ◽  
Author(s):  
VIVIEN CHAVANELLE ◽  
YOLANDA F. OTERO ◽  
PASCAL SIRVENT ◽  
PATRICE D. CANI ◽  
SEBASTIEN PELTIER
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