scholarly journals Separate Compartments for Chromosome Entrapment and DNA Binding during SMC translocation

2018 ◽  
Author(s):  
Roberto Vazquez Nunez ◽  
Laura B. Ruiz Avila ◽  
Stephan Gruber

SummaryMulti-subunit SMC ATPase complexes translocate on chromosomal DNA. They control chromosome structure and DNA topology, presumably by acting as DNA extrusion motors. The SMC-kleisin ring entraps chromosomal DNA. The ring lumen is strongly reduced in size by alignment of the SMC arms and upon ATP binding is divided in two by engagement of SMC head domains. Here, we provide evidence for DNA binding in the SMC compartment and chromosome entrapment in the Kleisin compartment of B. subtilis Smc/ScpAB. We show that DNA binding at the Smc hinge is dispensable and identify an essential DNA binding site at engaged heads which faces the S compartment. Mutations interfering with DNA binding do not prevent ATP hydrolysis but block DNA translocation by Smc/ScpAB. Our findings are consistent with the notion that Smc/DNA contacts stabilize looped DNA segments in the S compartment, while the base of a chromosomal DNA loop is enclosed in the K compartment. Transfer of DNA double helices between S and K compartments may support DNA translocation.

1992 ◽  
Vol 267 (35) ◽  
pp. 24941-24947
Author(s):  
J Zilliacus ◽  
A.P. Wright ◽  
U Norinder ◽  
J.A. Gustafsson ◽  
J Carlstedt-Duke

2002 ◽  
Vol 28 (3) ◽  
pp. 193-205 ◽  
Author(s):  
J Quirk ◽  
P Brown

The homeobox repressor Hesx1, expressed throughout Rathke's pouch and required for normal pituitary development, has been implicated in anterior pituitary pathogenesis in man. Prolonged expression of Hesx1 delays the appearance of anterior pituitary terminal differentiation markers in mice, particularly the gonadotroph hormones. We tested if Hesx1 could modulate gonadotrophin gene expression directly, and found that Hesx1 repressed both common alpha subunit (alpha GSU) and luteinising hormone beta-subunit (LH beta) gene promoters. Repression mapped to the Pitx1 homeodomain protein transactivation site in the proximal alpha GSU promoter, but did not map to the equivalent site on LH beta. Hesx1 repression of the alpha GSU Pitx1 site was overridden by co-transfection of Pitx1. In contrast, Hesx1 antagonised Pitx1 transactivation of LH beta in a dose-dependent manner. This was due to monomeric binding of Hesx1 on alpha GSU and homodimerisation on LH beta. The homodimerisation site comprises the Pitx1 DNA binding site and a proximal binding site, and mutation of either inhibited homodimer formation. Conversion of the LH beta Pitx1 DNA binding site to an alpha GSU-type did not promote homodimer formation, arguing that Hesx1 has pronounced site selectivity. Furthermore, mutation of the proximal half of the homodimerisation site blocked Hesx1 antagonisation of Pitx1 transactivation. We conclude that Hesx1 monomers repress gene expression, and homodimers block specific transactivation sites.


2000 ◽  
Vol 275 (35) ◽  
pp. 27013-27020
Author(s):  
Yan Wang ◽  
Jingshi Shen ◽  
Natalia Arenzana ◽  
Witoon Tirasophon ◽  
Randal J. Kaufman ◽  
...  

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