scholarly journals Wiring the Brain by Clustered Protocadherin Neural Codes

Author(s):  
Qiang Wu ◽  
Zhilian Jia

Abstract There are more than a thousand trillion specific synaptic connections in the human brain and over a million new specific connections are formed every second during the early years of life. The assembly of these staggeringly complex neuronal circuits requires specific cell-surface molecular tags to endow each neuron with a unique identity code to discriminate self from non-self. The clustered protocadherin (Pcdh) genes, which encode a tremendous diversity of cell-surface assemblies, are candidates for neuronal identity tags. We describe the adaptive evolution, genomic structure, and regulation of expression of the clustered Pcdhs. We specifically focus on the emerging 3-D architectural and biophysical mechanisms that generate an enormous number of diverse cell-surface Pcdhs as neural codes in the brain.

2007 ◽  
Vol 46 (22) ◽  
pp. 4180-4183 ◽  
Author(s):  
Hendrik Schroeder ◽  
Bernhard Ellinger ◽  
Christian F. W. Becker ◽  
Herbert Waldmann ◽  
Christof M. Niemeyer

2003 ◽  
Vol 92 (5) ◽  
pp. 234-241 ◽  
Author(s):  
D. James Morré ◽  
Dorothy M. Morré ◽  
Howard Sun ◽  
Raymond Cooper ◽  
Joseph Chang ◽  
...  

1984 ◽  
Vol 33 (2) ◽  
pp. 268-281 ◽  
Author(s):  
Ann M. Carroll ◽  
Michael Zalutsky ◽  
Sam Schatten ◽  
Atul Bhan ◽  
Linda L. Perry ◽  
...  

2010 ◽  
Vol 26 (6) ◽  
pp. 1544-1550
Author(s):  
Sandeep K. Arora ◽  
Rohit Sharma ◽  
Gagandeep Kaur ◽  
Preeti Bhoria ◽  
Maryada Sharma ◽  
...  

2018 ◽  
Vol 90 (10) ◽  
pp. 6131-6137 ◽  
Author(s):  
Baoyin Yuan ◽  
Yuanyuan Chen ◽  
Yuqiong Sun ◽  
Qiuping Guo ◽  
Jin Huang ◽  
...  

Development ◽  
1989 ◽  
Vol 105 (4) ◽  
pp. 795-802
Author(s):  
S.L. Goodman ◽  
R. Deutzmann ◽  
V. Nurcombe

The specific interaction of embryonal cells with the extracellular matrix (ECM) is one of the principal forces influencing embryonal development (Hay, 1984; Trinkaus, 1984). We used a muscle satellite cell line (MM14dy) to determine the relationship between locomotory response to laminin and the expression of specific cell surface binding sites for it. Time lapse videomicroscopic analysis was used to study the locomotory response and radioligand binding assays and cell attachment assays were used to follow the expression levels of binding sites for laminin and its subfragments E8 and E1–4. We report here the novel finding that the ability of MM14dy to locomote over laminin diminishes and finally vanishes as the cells differentiate. The simultaneous drop in expression of binding sites for laminin is interpreted as being of potential significance during development and repair.


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