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73-546: The BBSome is an eight-protein complex consisting of different subunits named Bardet-Biedl Syndrome (BBS) proteins after the ciliopathy disease caused by a mutation in BBS proteins. Currently, there are 24 discovered BBS gene products that either form the BBSome or interact with the BBSome. Several BBS proteins that are not associated with the BBSome (BBS11, BBS13, BBS15, BBS16, BBS19-24) have yet to be extensively studied. The proteins within

146-522: A GTP molecule will enter the cilia and drive ciliary membrane expansion. Blocking the production of Rab8-GTP can result in BBS symptoms occurring in organisms such as zebrafish. BBSome activity has recently been expanded to systems other than primary cilia transports and has been connected to renal, neuronal, vascular, and cardiac development, regulation, and function. The expression of BBS genes were seen in different tissues that relate to blood pressure, cardiovascular function, and renal activity. Mutations in

219-503: A decrease in vasorelaxation responses when exposed to acetylcholine leading to an increase in aortic pulse wave velocity. The deletion increased the vascular angiotensinogen gene expression in the aorta which activated the renin-angiotensin system and led to aorta stiffening. The high prevalence of cardiac disease in leading causes of death presents a very real need to further understand the relationship between BBSome function and cardiac health. BBSomes that are found in neurons can have

292-473: A higher renal sympathetic nerve activity (SNA) in the mice with the Bbs1 deletion in regular neurons and LRb neurons compared to the control mice. The higher SNA and increased body weight due to the deletion of BBS genes all contributed to the development of hypertension in the mice. Hypertension is a symptom that is often seen with and is the leading cause of death in BBS patients, so the understanding of how it develops

365-406: A major cause of morbidity and mortality. There is a wide range of secondary features that are sometimes associated with BBS including Findings in genetic research published in 2006 have suggested that a large number of genetic disorders , both genetic syndromes and genetic diseases , that were not previously identified in the medical literature as related, may be, in fact, highly related in

438-500: A primarily negative area, that all BBSome units other than BBS5 contribute, to be exposed in the center of the complex. The three main negatively charged areas are located where the GAE domain of BBS1 contacts the 5α domain of BBS9, deep in the BBSome core where there is an α-helix in the BBS18 domain, and where there is a higher concentration of glutamate and aspartate residues in the α-helix of

511-431: A separate entity. However, some recent research suggests that the two conditions may not be distinct. As of 2012 , 14 (or 15) different BBS genes had been identified. Basal body A basal body (synonymous with basal granule , kinetosome , and in older cytological literature with blepharoplast ) is a protein structure found at the base of a eukaryotic undulipodium ( cilium or flagellum ). The basal body

584-501: A significant role in the regulation of blood pressure. A person with BBS is about eight times more likely to develop hypertension compared to people without a BBS gene mutation with mutations in the BBS10 encoding gene have more dramatic increases in blood pressure. In fact, mutations in all of the BBS proteins, except BBS2, will lead to some level of hypertension. Hypertension is also seen in heterozygous BBS carriers which consists of about 1% of

657-559: A single missense mutation in the M390R location in the BBS1 gene representing about a 80% of the mutations in this gene. The remaining 20% have been diagnosed with the disease, but still require molecular diagnosis to determine the source of mutation causing the disease. One research study performed whole genome sequencing on 450 families with a history of BBS. Exons of their DNA samples were acquired, underwent high throughput sequencing, were aligned with

730-407: A study performed in 2007 that used biochemical purification of complexes that contained BBS4 in mammalian cells. The researchers identified BBSome localization to both centriolar satellites in the cytoplasm and the membrane of the cilia, the importance of the BBSome concerning IFT, and the mechanism for delivery to the cilia via centriolar satellites. They hypothesized that the BBSome was transported to

803-420: A variety of effects in certain cells. Mutations in the BBS1 and BBS10 genes are seen in about 70% of cases of patients of European descent. Even people without the BBSome dysfunction causing ciliopathy Bardert-Biedl Syndrome have been found to have certain symptoms of the disease such as obesity or hypertension due to variance or small mutations in some of the BBS genes. One particular mutation that has been studied

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876-576: A whole-genome mutagenesis screen identified two mutations in dyf-2 and bbs-1 which showed normal anterograde IFT but defective IFT turnaround at the tip prevents retrograde transport. One experiment showed that inhibiting the production of BBS5 lead to the absence of flagella in Chlamydomonas. When bbs4 mutants of Chlamydomonas were analyzed, researchers found that the cells showed normal flagellar structure, but had defective IFT transport. Bardet%E2%80%93Biedl syndrome Bardet–Biedl syndrome ( BBS )

949-473: A wide range of clinical variability observed both within and between families. The most common clinical features are rod–cone dystrophy , with childhood-onset night-blindness followed by increasing visual loss; postaxial polydactyly ; truncal obesity that manifests during infancy and remains problematic throughout adulthood; varying degrees of learning disabilities; male hypogenitalism and complex female genitourinary malformations; and renal dysfunction,

1022-485: A wide range of disease symptoms including those commonly seen in BBS patients, it is now widely accepted that mutated BBS genes affect normal cilia function, which, in turn, causes BBS. A theory that photoreceptor cells are nourished by the IFT of retinal cilia now offers a potential explanation for the retinal dystrophy common in BBS patients after their early years of life. Genes involved include: The diagnosis of BBS

1095-450: A wide range of effects on a person's health. One particularly studied avenue is the effect of neuronal BBSomes on blood pressure regulation. This study looked at mice with a Bbs1 deletion in regular neurons and neurons that specifically released the long signaling form of LRb (Leptin Receptor). The researchers noticed a sympathetic increase in blood pressure without an increase in heart rate and

1168-443: Is a ciliopathic human genetic disorder that produces many effects and affects many body systems. It is characterized by rod/cone dystrophy , polydactyly , central obesity , hypogonadism , and kidney dysfunction in some cases. Historically, slower mental processing has also been considered a principal symptom but is now not regarded as such. Bardet–Biedl syndrome is a pleiotropic disorder with variable expressivity and

1241-544: Is an autosomal recessive disorder that occurs in about 1 in every 100,000 live births and is due to homozygous mutations in any of the BBS genes other than BBIP1. These mutations often lead to the incorrect formation of the BBSome which then has subsequent effects on cargo trafficking and IFT regulation. The results of this mutation can range from blindness to deafness to a lack of smell. The visual impairment can include difficulties in light perception, dense cataracts, or retinal dystrophy. Symptoms can also include obesity, which

1314-489: Is believed that the BBSome assembles sequentially, beginning with the association of BBS7, BBS chaperonins, and the CCT/TRiC complex, which functions as a scaffold to which further subunits can bind. BBS2 and BBS7 bind together first. BBS2 and BBS7 are missing in certain species, such as Drosophila, which leads to the idea that they might be more important in organizing the BBSome in higher organisms rather than directly related to

1387-560: Is critical. The researchers discovered that a deletion of the IFT88 gene, which is a key protein for the IFT-B complex, also showed an increased body weight but had no effect on the blood pressure or sympathetic nerve reaction showing that the BBSome involvement in cilia formation is not what is causing the observed symptoms. The structure and composition of BBSomes vary across species and different types of cells, which leads to different mutations having

1460-419: Is essential for ciliogenesis and the maintenance of cilia. Recent biochemical analysis of human BBS proteins revealed that BBS proteins are assembled into a multiple protein complex, called "BBSome". BBSome is proposed to be responsible for transporting intracellular vesicles to the base of the cilia and to play an important role in the ciliary function. Since abnormalities of cilia are known to be related to

1533-462: Is established by clinical findings and family history. Molecular genetic testing can be used to confirm the diagnosis. Multigene panels offer the most effective approach in achieving molecular confirmation of BBS. There is currently no specific treatment but it is important that an experienced multidisciplinary team manages patients with adequate supportive treatments. The syndrome is named after Georges Bardet and Arthur Biedl after they reported

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1606-548: Is potentially related to the increase in LDL cholesterol, decrease in HDL levels, and increase C peptide concentrations that have been observed in BBS patients. The primary cilia are required for the Hedgehog signaling pathway. This pathway plays a vital role during vertebrate embryonic development and directly affects the development of limbs and digits. The nonfunctional BBSome that results from

1679-407: Is still a lot about the mechanism in which it functions that remain unknown. The identity of which cilia membrane proteins require the BBSome, the molecular and/or enzymatic activity of the complex, the specific function of BBS proteins that are not within the BBSome, as well as many other questions still need to be answered for the complete understanding of what the BBSome is and how it functions. It

1752-412: Is still unclear. The gene products encoded by these BBS genes, called BBS proteins, are located in the basal body and cilia of the cell . Using the round worm C. elegans as a model system, biologists found that BBS proteins are involved in a process called intraflagellar transport (IFT), a bi-directional transportation activity within the cilia along the long axis of the ciliary shaft that

1825-459: Is the p. Leu 58* mutation in the expression of BBIP1 gene products. This mutation eliminates the helix that ties BBS18 to BBS1. It has been shown that this leads to dysfunction in the assembly of the BBSome which can have detrimental effects on systems outside of ciliary transport. Mutations in the BBS17/LZTFL1 or BBS3/Arl6 genes have shown to have a detrimental effect on trafficking proteins to

1898-622: The centrosome . Then, the BBSome can dissociate from PMC-1 and perform its function in the basal body or within the primary cilia. The researchers believed the complex consisted of seven proteins (BBS1, BBS2, BBS4, BSS5, BBS7, BBS8, and BBS9). They also discovered the relationship between the subunits of interactions of BBS1/BBS2/BBS7 with β-propeller domains, BBS4/BBS8 with TPR ( tetratricopeptide repeat) regions, BBS3/Arl6, and BBS6/BBS10/BBS12 relations for chaperonin-like functions. They noticed that BBS9 interacted with several other subunits like BBS1, BBS2, BBS4, BBS5, and BBS8, so they proposed that it

1971-506: The genetypical root cause of the widely varying, phenotypically observed disorders . BBS is one such syndrome that has now been identified to be caused by defects in the cellular ciliary structure . Thus, BBS is a ciliopathy . Other known ciliopathies include primary ciliary dyskinesia , polycystic kidney and liver disease , nephronophthisis , Alström syndrome , Meckel–Gruber syndrome and some forms of retinal degeneration . The detailed biochemical mechanism that leads to BBS

2044-492: The microtubule organizing center (MTOC). These microtubules provide structure and facilitate movement of vesicles and organelles within many eukaryotic cells. Cilia and basal bodies form during quiescence or the G1 phase of the cell cycle . Before the cell enters G1 phase, i.e. before the formation of the cilium, the mother centriole serves as a component of the centrosome . In cells that are destined to have only one primary cilium,

2117-638: The BBS genes will also result in Bardet-Biedl Syndrome. Ciliary BBSomes can affect obesity levels, ciliary BBSomes in nephronal tissue can affect kidney health, neuronal BBSomes can play an important role in regulating blood pressure, and BBSomes in vascular and cardiac cells can also affect arterial pressure and heart development. All of these effects are seen in patients with BBS, but BBS gene polymorphism can be associated with complications in blood pressure, body weight, and other cardiovascular factors in patients that do not have BBS. Bardet-Biedl Syndrome

2190-428: The BBS1 β-propeller. The complexity of the BBSome structure, especially in the binding recognition site, shows the specificity of the binding relationships and activities of the complex. This created area facilitates the binding of the cargo proteins with their positively charged signaling sequences. These positively charged domains, made of aromatic and basic residues, are mainly located in the third intracellular loop and

2263-412: The BBS18 domain clamps the other two subunits in a Y-shaped layout that serves as the backbone for the BBSome complex. It is critical for the stability and assembly of the BBSome, particularly with stabilizing the interactions between BBS4 and BBS8. BBS8 has a loop in its domain that is different across purified BBSomes which leads to the idea that this domain might be involved in tissue specific activity of

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2336-490: The BBSome function of assembling the IFT machinery. An experiment performed with Caenorhabditis elegans looked at GFP -tagged IFT-B protein complexes to look for IFT-B accumulation at the tip of the primary cilia in organisms with inhibited IFT turnaround. The defective (Dyf) C. elegans mutants showed a dissociation between the BBSome and IFT particles causing BBS proteins to accumulate at the ciliary base, regular anterograde transport, but an accumulation of IFT-B components at

2409-420: The BBSome subunits to be collected when the BBSome is active (Arl6 bound). High-resolution cryo-electron microscopy with an average of 3.8 Å was used to display the overall complex structure, but it did not allow for an accurate atomic model due to limited resolution. Only approximately 80% of the complex could be described using an atomic model. Due to the relatively recent discovery of the protein complex, there

2482-593: The BBSome. The C-terminal helix of BBS18 also loosely interacts with the gamma-adaptin ear (GAE) domain of BBS1, the most relevant domain to cargo recognition, to also aid with structure of the complex. BBS1 then binds its N-terminal β-propeller domain to the N-terminal of the BBS4 TPR superhelix, a connection which is stabilized by hydrophobic interactions. It wraps around the BBS4 and BBS8 domains and binds its C-terminal GAE domain to

2555-471: The C-terminal domain of ciliary GPCRs. The position of the positively charged sequences end up close to BBS1, which is also essential in cargo protein recognition. Rabin8 is a guanine nucleotide exchange factor for Rab8 necessary for ciliogenesis in primary cilia. Rab family GTPases usually assist in vesicular trafficking by promoting the docking and binding of vesicles to their target. Rabin8 helps localize

2628-553: The C-terminal hairpin in BBS9 and the β-propeller of BBS1 to form a lobe at the top of the complex to block the Arl6 binding site on the BBS1 subunit. This is the formation of the BBSome complex when it is not needed for IFT regulation. When the BBSome is needed, the BBS2 and BBS7 dome moves to allow for binding the membrane-associated GTPase Arl6 and the activation of the BBSome. Arl6 recruits the BBSome to

2701-496: The N-terminal β-propeller of BBS1. BBS17 can also help promote BBS3 to the basal body, which in turn controls the amount of BBSome available for anterograde IFT into the cilia. Arl6 is an ARF(ADP Ribosylation Factor)-like GTPase that helps recruit the BBSome to the ciliary membranes. It is comparable to Arf1 and Sar1 in COPI/COPII and clathrin coats. The BBSome complex begins with a conformation that has BBS2 and BBS7 interacting at

2774-569: The TPR domain of BBS8. BBS9 associates in a similar but reciprocal manner with its N-terminal β-propeller domain bound to the N-terminus of the TPR superhelix of BBS8. BBS9 then wraps around BBS4 and parts of BBS1 and binds its C-terminal GAE to the GAE domain of BBS1. BBS9 also interacts with BBS1 to create an open area within the core complex to allow for the wrapping of BBS1 around the BBS4 and BBS8 subunits. Their C-terminal domains interact with one another so

2847-409: The appendages of mother centriole. In multiciliated cells, however, in many cases basal bodies are not made from centrioles but are generated de novo from a special protein structure called the deuterosome . During cell cycle dormancy, basal bodies organize primary cilia and reside at the cell cortex in proximity to plasma membrane. On cell cycle entry, cilia resorb and the basal body migrates to

2920-408: The assembly of the BBSome in an ATP-dependent manner. BBS3 associates with Arl6 (ARF-like 6) and helps in recruiting the BBSome to ciliary membranes. BBS7 interacts with LZTFL1 (Leucine Zipper Transaction Factor-Like 1) to regulate the entry of the BBSome into the primary cilia. The BBSome has a similar structure and function compared to COPI , COPII , and clathrin coats showing its similarity to

2993-619: The basal body and promote ciliogenesis and Rab8 association with vesicles coming from the Golgi Body to help with target complex combination by facilitating the binding of GTP to Rab8. The BBSome, specifically the interaction between the BBS1 subunit and the C-terminus of Rabin8, is thought to aid with the GEF activity of Rabin8 to direct vesicles leaving the Golgi Body to the base of the cilia. Rab8 bound to

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3066-437: The basal body by centriolar satellites, which are cytoplasmic granules that bring specific proteins to the centrosome due to its connection to PCM-1. They proposed the use of centriolar satellites to transport the BBSome was to function in a chaperone-like manner to limit BBSome activity to the basal body . The researchers noticed that BBS4 interacts with PCM-1, a core component of centriolar satellites, and helps bring proteins to

3139-413: The cargo and membrane binding functions of the BBSome. Then, BBS9 is added to the core complex followed by BBS5 and BBS8. BBIP1, also known as BBS18, is the smallest subunit that is located in the center of the complex. This protein domain winds through two super-helically arranged (TPR) domains of the BBS4 and BBS8 subunits, which are arranged perpendicularly and stabilized by ionic interactions. Together,

3212-441: The cells in the nephron and on the apical surface of epithelial cells in the lumen of the kidney which leads to the connection of BBSome function with renal activity. All BBS protein mutations, except BBS2, will result in renal dysfunction with more severe renal diseases coming from mutations in the BBS chaperonin genes. Approximately 82% of people diagnosed with BBS have shown symptoms of some form of kidney defectiveness. The cilia on

3285-461: The cilia without having an effect on the assembly of the BBSome. Zebrafish have been used to study BBS function and mutations. A study on the importance between Rab8-GTP production to BBS was performed when scientists injected mRNAs coding for Rab8 mutations into one-cell zebrafish embryos. These mutations end in abnormalities in Kupffer's vesicle which is analogous to the node in humans and contributes to

3358-427: The ciliary base and mediates the bidirectional movement, all of which sustains the success of IFT. IFT-A controls retrograde IFT, and IFT-B controls anterograde transport. DYF-2 is a protein that functions with BBS1 to stabilize the interaction between the BBSome and the IFT complex in preparation for retrograde transport. In mutants with nonfunctional BBSome proteins, IFT-B can not associate with IFT-A, which demonstrates

3431-425: The ciliary tip due to an absence of the BBSome. BBS gene expression has been observed in nonciliated cells in cardiac, vascular, and renal tissues, which expands the parameters of the BBSome functions to cellular processes other than solely primary cilia protein transport, such as plasma membrane receptor localization, gene expression, and cell division. The discovery that BBS7, and other BBS proteins, like BBS4, enter

3504-468: The common link. A study was performed using a mouse model to analyze the effects of BBSome activity dysfunction in smooth muscle cells through the deletion of the Bbs1 gene on vascular function, blood pressure, and arterial stiffening. The results showed heightened contractility of the vascular rings and an increase in arterial stiffness.due to enhanced endothelin-1 -induced contractility of mesenteric arteries . The aortic rings of mice with Bbs1 mutations had

3577-482: The correct cardiac looping with defects in the BBSome function leading to situs inversus and randomized cardiac looping. Looking at the involvement of BBS6 in overseeing the SWI/SNF chromatin remodeling complex has provided signs that this BBS protein, and potentially others, could lead to heart disease in patients without BBS. BBSome presence in vascular smooth muscle has been shown to affect vascular reactivity and plays

3650-452: The course of the study due to the lack of leptin receptors that could be transported to the cilia for environment signaling. The BBSome also traffics the insulin receptor, so insufficient BBSome function reduces the insulin receptor expression which translates into reduced signaling. This leads to deficiencies in glucose metabolism, insulin resistance, and the proliferation of diabetes in BBS patients. Primary cilia have been observed on most of

3723-461: The development of glomerular cysts. The BBSome has also been connected to cardiac development and maintenance, with particular function in the renin-angiotensin system, due to its high prevalence in people with BBS. Different defects that have been explored in connection with the BBSome are dilated cardiomyopathy , aortic valve stenosis , and hypertrophy of the interventricular septum . The BBSome has also been related to left-right patterning and

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3796-466: The eighth subunit in the BBSome. Bardet-Biedl Syndrome has also been related to hypertension and other cardiovascular complications. BBSome dysfunction has been shown to cause obesity in mouse models as well as humans with BBS. Leptin is a hormone that is released from adipose tissue to monitor feeding behavior. The BBSome, specifically BBS1, was shown to interact with the C-terminal cytoplasmic receptors of leptin receptors (LebRb) to transport them to

3869-681: The endothelial cells survey the blood flow to the kidney. Any dysfunction in the BBSome can lead to a shorter primary cilia and a reduction in epithelial turnover and repair leading to different cystic kidney diseases , decrease in the ability to process creatine out of the body, and the inability to filter waste products that are often paired with hypertension development. The renal anomalies that can arise due to BBS deficiencies can cause serious medical problems that may lead to dialysis or kidney transplantation. A study with knockout Bbs4 gene in mice resulted in decreased urine production and increased sodium and blood urea nitrogen concentrations leading to

3942-591: The first official cases in 1920 and 1922. The first known case was reported by Laurence and Moon in 1866 at the Ophthalmic Hospital in South London. Laurence–Moon–Biedl–Bardet syndrome is no longer considered as valid terms in that patients of Laurence and Moon had paraplegia but no polydactyly or obesity, which are the key elements of the Bardet–Biedl syndrome. Laurence–Moon syndrome is usually considered

4015-411: The function of these vesicle-forming complexes in transporting proteins. All BBS proteins are highly conserved in genetics which shows their importance in primary cilium biogenesis and intraflagellar transport (IFT). The BBSome links cargo proteins to intraflagellar transport (IFT) machinery, which transports structural components and receptors, with the help of motor proteins dynein and kinesin , from

4088-492: The human reference genome, and single nucleotide polymorphism calling was performed. Approximately 15% of the subjects did not have any mutations in the BBS genes, but the remaining percentage of the subjects contained nonsense , frame-shift , splice , missense , and in- frame deletion mutations. The primary mutation that led to a nonfunctional BBSome was a nonsense mutation in the BBIP1 gene dubbed p. Leu 58* which encodes for

4161-459: The inversion of organ laterality. The nonfunctional BBSome leads to defects in the primary cilia that covers Kupffer's vesicle, a complex that is responsible for instituting left and right asymmetry of the brain, heart, and gut in zebrafish during embryonic development. The lack of BBSome functionality also caused delays in dynein-dependent retrograde transport of melanosomes , organelles that synthesize and contain melanin. A study on C. elegans with

4234-748: The largest and most stable BBSome core complex are BBS1, BBS4, BBS5, BBS8, BBS9, and BBS-interacting protein BBIP1, also known as BBS18. BBIP1 is the proposed eighteenth BBS gene due to its essential role in interacting with the BBSome and reduced levels in patients with a BBS diagnosis. BBS2 and BBS7 are also within the BBSome but are more loosely associated, which leads to their exclusion in the core complex. Other BBSome-associated proteins can be found in higher-level organisms with more IFT requirements. For example, BBS6, BBS10, and BB12 form into chaperonin complexes with CCT/TRiC (chaperonin-containing tailless complex polypeptide 1/tailless complex polypeptide 1 ring complex) in chordates which function to regulate and oversee

4307-411: The membrane and binds to the peripheral N-terminal β-propeller domain of BBS1, which functions in ciliary cargo protein recognition but is not directly involved in cargo loading. This change in shape allows the region of the BBSome that is prominently positive to be near the membrane, which helps with the association of the complex to the negatively charged ciliary membrane. The conformation also allows for

4380-450: The mother centriole differentiates into the basal body upon entry into G1 or quiescence. Thus, the basal body in such a cell is derived from the centriole. The basal body differs from the mother centriole in at least 2 aspects. First, basal bodies have basal feet, which are anchored to cytoplasmic microtubules and are necessary for polarized alignment of the cilium. Second, basal bodies have pinwheel-shaped transition fibers that originate from

4453-466: The mutations in any of the seven BBS proteins inhibits the hedgehog pathway leading to post-axial polydactyly (meaning the extra digit occurs on the outside of the hand or foot) or brachydactyly where the digits are shorter than normal. More potential symptoms include kidney failure, retinitis pigmentosa , behavioral dysfunction, and hypogonadism . Mutations in one of 19 known BBS genes is present in 80% of patients that have been diagnosed with BBS, with

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4526-409: The nucleus and, in the case of BBS7, interact with ring finger protein 2 ( RNF2 ) to regulate its transcription supports the concept that the BBSome might also be involved in gene expression. It is not yet definitive on whether this gene expression role is separate from the BBSome transportation of proteins function. It was discovered by Maxence Nachury, Alexander Loktev, and several other associates in

4599-524: The nucleus where it functions to organize centrosomes. Centrioles, basal bodies, and cilia are important for mitosis, polarity, cell division, protein trafficking, signaling, motility and sensation. Mutations in proteins that localize to basal bodies are associated with several human ciliary diseases, including Bardet–Biedl syndrome , orofaciodigital syndrome , Joubert syndrome , cone-rod dystrophy , Meckel syndrome , and nephronophthisis . Regulation of basal body production and spatial orientation

4672-418: The only BBS subunit that can bind to phosphoinositides and PAs. The lack of the presence of BBS2, BBS7, and BBS5 in all of the isolated BBSomes shows that these subunits are most likely not required for all stages of the functionality of the BBSome. BBS3 collaborates with Arl6 to control the BBSome recruitment to the membrane and the entry and exit to and from the cilia. When BBS3 is bound to GTP, it can bind to

4745-416: The plasma membrane. A mutation named M390R, which is the most commonly seen BBS1 mutation observed in BBS patients, significantly decreased the potential for BBS1 to interact with LepRb. This reduced the amount of LepRb surface expression which affects appetite, food intake, and energy output. BBS10 was also seen to promote the stability of LepRb by increasing its translation of decreasing its degradation. BBS17

4818-468: The population. Studies involving mice with BBS gene deletions have shown that mutations or defects in the BBSome activity can lead to cardiovascular issues like hypertension. Elevated blood pressure has been seen in mice with BBS3, BBS4, and BBS6 deletions, but was absent in mice with BBS2 deletions. These mice were also shown to have an increase in renal sympathetic nerve activity, linking the sympathetic nervous system to hypertension with BBSome dysfunction as

4891-418: The subunits to the function of the protein complex. BBS5 has two pleckstrin homology (PH) domains that can bind to phosphoinositides, mainly phosphatidylinositol 3-phosphate (PI3P) and phosphatidic acid (PA), which are thought to be essential for cilia biogenesis. These PH regions can also interact with the β-propeller of BBS9. BBS5 is seen to be more loosely associated with the core complex, which led to

4964-435: The suggestion that it most likely assists with the BBSome making contact with membranes through the bound phosphoinositides to regulate the BBSome transportation in the cilium. BBS5 on one side of the complex allows for binding to the ciliary membrane, while the Arl6 binding side on the opposite site of the complex can bind cargo. The discovery that BBS5 is missing in particular natively purified BBSomes reveals that it may not be

5037-399: The tip to the base of the primary cilia (anterograde transport) and back (retrograde transport) along ciliary microtubules. Since cilia cannot synthesize proteins, the IFT pathway is required for biogenesis, maintenance, and signaling within the cilia through motors, IFT-A and IFT-B subcomplexes, and the cargo proteins. The BBSome assists with the assembly and stabilization of the IFT complex at

5110-467: The β-propeller domains are facing the outside of the complex to interact with the TPR domains of BBS4 and BBS8. Certain pathogenic mutations like Q439H, Q445K, or L518P can disrupt the interaction between the BBS8, BBS9, and BBS1 domains causing an improper association of the subunits and a nonfunctional BBSome. The necessity of having a properly assembled BBSome highlights the importance of the interactions between

5183-495: Was found to function in the regulation of LebRb activating Stat3 transcription factor in relation to leptin sensitivity. This system of leptin expression and regulation is a BBSome pathway that is independent of cilia, showing the diverse and greatly unknown applications for the complex. A study performed with mice that had a nonfunctional BBSome were found to be incapable of transducing leptin signals in certain hypothalamic neurons. The mice used in this experiment gained weight over

5256-453: Was located in the center of the complex. They also noticed how the BBSome function was linked to Rabin8, a protein that localizes the basal body and attracts the BBSome protein BBS1. The scientists then looked at BBS5 to determine the areas of the BBSome that function in lipid binding and noticed how the binding of phosphoinositides might be essential for ciliogenesis. Arl6's crystal structure allowed for high-resolution structural information on

5329-399: Was named by Theodor Wilhelm Engelmann in 1880. It is formed from a centriole and several additional protein structures, and is, essentially, a modified centriole. The basal body serves as a nucleation site for the growth of the axoneme microtubules. Centrioles, from which basal bodies are derived, act as anchoring sites for proteins that in turn anchor microtubules , and are known as

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