RAD21

Double-strand-break repair protein rad21 homolog is a protein that in humans is encoded by the ''RAD21'' gene. ''RAD21'' (also known as ''Mcd1'', ''Scc1'', ''KIAA0078'', ''NXP1'', ''HR21''), an essential gene, encodes a DNA double-strand break (DSB) repair protein that is evolutionarily conserved in all eukaryotes from budding yeast to humans.  RAD21 protein is a structural component of the highly conserved cohesin complex consisting of RAD21, SMC1A, SMC3, and SCC3 STAG1 (SA1) and STAG2">STAG1.html" ;"title="STAG1">STAG1 (SA1) and STAG2 (SA2) in multicellular organisms] proteins, involved in Establishment of sister chromatid cohesion, sister chromatid cohesion.

Discovery

''rad21'' was first cloned by Birkenbihl and Subramani in 1992 by complementing the radiation sensitivity of the ''rad21-45'' mutant fission yeast, ''Schizosaccharomyces pombe'', and the murine and human homologs of ''S. pombe'' rad21 were cloned by McKay, Troelstra, van der Spek, Kanaar, Smit, Hagemeijer, Bootsma and Hoeijmakers.  The human ''RAD21'' (''hRAD21'') gene is located on the long (q) arm of chromosome 8 at position 24.11 (8q24.11).  In 1997, RAD21 was independently discovered by two groups to be a major component of the chromosomal cohesin complex, and its dissolution by the cysteine protease Separase at the metaphase to anaphase transition results in the separation of sister chromatids and chromosomal segregation.

Structure

RAD21, belongs to a superfamily of eukaryotic and prokaryotic proteins called a-Kleisins, is a nuclear phospho-protein, ranges in size from 278aa in the house lizard ('' Gekko Japonicus'') to 746aa in the killer whale (''Orcinus Orca''), with a median length of 631aa in most vertebrate species including humans.  RAD21 proteins are most conserved at the N-terminus (NT) and C-terminus (CT), which bind to SMC3 and SMC1, respectively. The STAG domain in the middle of RAD21, which binds to SCC3 ( SA1/ SA2), is also conserved (Figure 1). These proteins have nuclear localization signals, an acidic-basic stretch and an acidic stretch (Figure 1), which is consistent with a chromatin-binding role. RAD21 is cleaved by several proteases including Separase and Calcium-dependent cysteine endopeptidase Calpain-1 during mitosis and Caspases during apoptosis.

Interactions

RAD21 binds to the V-shaped SMC1 and SMC3 heterodimer, forming a tripartite ring-like structure, and then recruits SCC3 (SA1/SA2). The 4 element-complex is called the cohesin complex (Figure 2).  Currently, there are two major competing models of sister chromatid cohesion (Figure 2B).  The first one is the one-ring embrace model, and the second one is the dimeric handcuff-model. The one-ring embrace model posits that a single cohesin ring traps two sister chromatids inside, while the two-ring handcuff model proposes trapping of each chromatid individually.  According to the handcuff model, each ring has one set of RAD21, SMC1, and SMC3 molecules. The handcuff is established when two RAD21 molecules move into anti-parallel orientation that is enforced by either SA1 or SA2.

The N-terminal domain of RAD21 contains two α-helices that forms a three helical bundle with the coiled coil of SMC3. The central region of RAD21 is thought to be largely unstructured but contains several binding sites for regulators of cohesin. This includes a binding site for SA1 or SA2, recognition motifs for separase, caspase, and calpain to cleave, as well as a region that is competitively bound by PDS5A, PDS5B or NIPBL.  The C-terminal domain of RAD21 forms a winged helix that binds two β-sheets in the Smc1 head domain.

WAPL releases cohesin from DNA by opening the SMC3-RAD21 interface thereby allowing DNA to pass out of the ring.  Opening of this interface is regulated by ATP-binding by the SMC subunits. This causes the ATPase head domains to dimerise and deforms the coiled coil of SMC3 therefore disrupting the binding of RAD21 to the coiled coil.

A total of 285 RAD21-interactants have been reported that function in wide range of cellular processes, including mitosis, regulation of apoptosis, chromosome dynamics, chromosomal cohesion, replication, transcription regulation, RNA processing, DNA damage response, protein modification and degradation, and cytoskeleton and cell motility (Figure 3).

Function

RAD21 plays multiple physiological roles in diverse cellular functions (Figure 4).  As a subunit of the cohesin complex, RAD21 is involved in sister chromatid cohesion from the time of DNA replication in S phase to their segregation in mitosis, a function that is evolutionarily conserved and essential for proper chromosome segregation, chromosomal architecture, post-replicative DNA repair, and the prevention of inappropriate recombination between repetitive regions. RAD21 may also play a role in spindle pole assembly during mitosis and progression of apoptosis. In interphase, cohesin may function in the control of gene expression by binding to numerous sites within the genome. As a structural component of the cohesin complex, RAD21 also contributes to various chromatin-associated functions, including DNA replication, DNA damage response (DDR), and most importantly, transcriptional regulation.  Numerous recent functional and genomic studies have implicated chromosomal cohesin proteins as critical regulators of hematopoietic gene expression.

As a part of cohesin complex, functions of Rad21 in the regulation of gene expression include: 1) allele-specific transcription by interacting with the boundary element CCCTC-binding factor (CTCF), 2) tissue-specific transcription by interacting with tissue-specific transcription factors, 3) general progression of transcription by communicating with the basal transcription machinery, and 4) RAD21 co-localization with CTCF-independent pluripotency factors (Oct4, Nanog, Sox4, and KLF2). RAD21 cooperates with CTCF, tissue-specific transcription factors, and basal transcription machinery to regulate transcription dynamically. Also, to effectuate proper transcription activation, cohesin loops chromatin to bring two distant regions together. Cohesin may also act as a transcription insulator to ensure repression. Thus, RAD21 can affect both activation and repression of transcription.  Enhancers that promote transcription and insulators that block transcription are located in conserved regulatory elements (CREs) on chromosomes, and cohesins are thought to physically connect distant CREs with gene promoters in a cell-type specific manner to modulate transcriptional outcome.

In meiosis, REC8 is expressed and replaces RAD21 in the cohesin complex. REC8-containing cohesin generates cohesion between homologous chromosomes and sister chromatids which can persist for years in the case of mammalian oocytes. RAD21L is a further paralog of RAD21 that has a role in meiotic chromosome segregation.  The major role of Rad21L cohesin complex is in homologue pairing and synapsis, not in sister chromatid cohesion, whereas Rec8 most likely functions in sister chromatid cohesion.  Intriguingly, concomitantly with the disappearance of RAD21L, Rad21 appears on the chromosomes in late pachytene and mostly dissociates after diplotene onward. The function of Rad21 cohesin that transiently appears in late prophase I is unclear.

Germline heterozygous or homozygous missense mutations in ''RAD21'' have been associated with human genetic disorders, including developmental diseases such as Cornelia de Lange syndrome and chronic intestinal pseudo-obstruction called Mungan syndrome, respectively, and collectively termed as cohesinopathies.  Somatic mutations and amplification of the ''RAD21'' have also been widely reported in both human solid and hematopoietic tumors.

Notes

References

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