Genomic Structure and Function of the UDP-Glucuronosyltransferases

Author(s):  
Lance B. Augustin ◽  
Clifford J. Steer
2008 ◽  
Vol 36 (19) ◽  
pp. 6035-6047 ◽  
Author(s):  
J. Singh ◽  
A. Saxena ◽  
J. Christodoulou ◽  
D. Ravine

2021 ◽  
Author(s):  
Jacob L. Steenwyk ◽  
Megan A. Phillips ◽  
Feng Yang ◽  
Swapneeta S. Date ◽  
Todd Graham ◽  
...  

Gene coevolution - which refers to gene pairs whose evolutionary rates covary across speciation events - is often observed among functionally related genes. We present a comprehensive gene coevolution network inferred from the examination of nearly three million gene pairs from 332 budding yeast species spanning ~400 million years of eukaryotic evolution. Modules within the network provide insight into cellular and genomic structure and function, such as genetic pleiotropy, genes functioning in distinct cellular compartments, vesicle transport, and DNA replication. Examination of the phenotypic impact of network perturbation across 14 environmental conditions using deletion mutant data from the baker's yeast Saccharomyces cerevisiae suggests that fitness in diverse environments is impacted by gene neighborhood and gene connectivity. By mapping the network onto the chromosomes of S. cerevisiae and the opportunistic human pathogen Candida albicans, which diverged ~235 million years ago, we discovered that coevolving gene pairs are not clustered in either species; rather, they are most often located on different chromosomes or far apart on the same chromosome. The budding yeast gene coevolution network captures the hierarchy of eukaryotic cellular structure and function, provides a roadmap for genotype-to-phenotype discovery, and portrays the genome as an extensively linked ensemble of genes.


2011 ◽  
Vol 43 (3) ◽  
pp. 346-361 ◽  
Author(s):  
Yasuhiro Uno ◽  
Kazuhide Iwasaki ◽  
Hiroshi Yamazaki ◽  
David R. Nelson

Author(s):  
Peter Sterling

The synaptic connections in cat retina that link photoreceptors to ganglion cells have been analyzed quantitatively. Our approach has been to prepare serial, ultrathin sections and photograph en montage at low magnification (˜2000X) in the electron microscope. Six series, 100-300 sections long, have been prepared over the last decade. They derive from different cats but always from the same region of retina, about one degree from the center of the visual axis. The material has been analyzed by reconstructing adjacent neurons in each array and then identifying systematically the synaptic connections between arrays. Most reconstructions were done manually by tracing the outlines of processes in successive sections onto acetate sheets aligned on a cartoonist's jig. The tracings were then digitized, stacked by computer, and printed with the hidden lines removed. The results have provided rather than the usual one-dimensional account of pathways, a three-dimensional account of circuits. From this has emerged insight into the functional architecture.


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