Entry - *620078 - FAMILY WITH SEQUENCE SIMILARITY 168, MEMBER B; FAM168B - OMIM
 
* 620078

FAMILY WITH SEQUENCE SIMILARITY 168, MEMBER B; FAM168B


Alternative titles; symbols

MYELIN-ASSOCIATED NEURITE OUTGROWTH INHIBITOR; MANI


HGNC Approved Gene Symbol: FAM168B

Cytogenetic location: 2q21.1     Genomic coordinates (GRCh38): 2:131,047,876-131,093,460 (from NCBI)


TEXT

Description

FAM168B modulates neurogenesis and neurite outgrowth (Mishra et al., 2011).


Cloning and Expression

By bioinformatic analysis, Mishra et al. (2011) showed that FAM168B, which they called MANI, contains 2 potential transmembrane domains, a potential opioid receptor (see 600018)-like motif, an acetylation site, and several phosphorylation sites. Topologically, MANI has a large extracellular loop, with its short N and C termini in the cytoplasm. RT-PCR and immunohistochemical analyses revealed that MANI was expressed in human brain tissue, specifically in myelinated neurons. Analysis with mouse brain showed that Mani was an N-glycoprotein that localized to neuronal cell membranes.

By immunocytochemical analysis, Mishra et al. (2012) showed that Mani localized to the perinuclear area and to the cell membrane of differentiated rat neuronal B104 cells.


Mapping

Gross (2022) mapped the FAM168B gene to chromosome 2q21.1 based on an alignment of the FAM168B sequence (GenBank BC066347) with the genomic sequence (GRCh38).


Gene Function

Mishra et al. (2011) showed that MANI expression was downregulated in brains of patients with Alzheimer disease (AD; 104300), as well as in brains of an AD mouse model. Ectopic expression of human MANI in catecholaminergic PC12 cells induced alterations in phosphorylation and the cleavage pattern of App (104760). Mani was not expressed in mouse neural stem cells (NSCs), but it was expressed in differentiated neurons and promoted their survival. Mani overexpression promoted NSC differentiation and neurogenesis, and it inhibited neurite outgrowth through Stmn2 (600621) and Stat3 (102582) in catecholaminergic PC12 cells. Furthermore, Mani interacted with Cdc27 (116946) to modulate the cell cycle, thereby regulating survival and differentiation of neurons.

Mishra et al. (2012) showed that Mani inhibited neurite outgrowth, as knockdown of Mani in primary rat cortical neurons had significantly longer neurites than controls. A yeast-2-hybrid screen revealed that Mani interacted with several proteins involved in governing neurite outgrowth.


REFERENCES

  1. Gross, M. B. Personal Communication. Baltimore, Md. 10/13/2022.

  2. Mishra, M., Akatsu, H., Heese, K. The novel protein MANI modulates neurogenesis and neurite-cone growth. J. Cell. Molec. Med. 15: 1713-1725, 2011. [PubMed: 20716133, images, related citations] [Full Text]

  3. Mishra, M., Lee, S., Lin, M. K., Yamashita, T., Heese, K. Characterizing the neurite outgrowth inhibitory effect of Mani. FEBS Lett. 586: 3018-3023, 2012. [PubMed: 22771904, related citations] [Full Text]


Contributors:
Matthew B. Gross - updated : 10/13/2022
Creation Date:
Bao Lige : 10/13/2022
alopez : 10/14/2022
mgross : 10/13/2022

* 620078

FAMILY WITH SEQUENCE SIMILARITY 168, MEMBER B; FAM168B


Alternative titles; symbols

MYELIN-ASSOCIATED NEURITE OUTGROWTH INHIBITOR; MANI


HGNC Approved Gene Symbol: FAM168B

Cytogenetic location: 2q21.1     Genomic coordinates (GRCh38): 2:131,047,876-131,093,460 (from NCBI)


TEXT

Description

FAM168B modulates neurogenesis and neurite outgrowth (Mishra et al., 2011).


Cloning and Expression

By bioinformatic analysis, Mishra et al. (2011) showed that FAM168B, which they called MANI, contains 2 potential transmembrane domains, a potential opioid receptor (see 600018)-like motif, an acetylation site, and several phosphorylation sites. Topologically, MANI has a large extracellular loop, with its short N and C termini in the cytoplasm. RT-PCR and immunohistochemical analyses revealed that MANI was expressed in human brain tissue, specifically in myelinated neurons. Analysis with mouse brain showed that Mani was an N-glycoprotein that localized to neuronal cell membranes.

By immunocytochemical analysis, Mishra et al. (2012) showed that Mani localized to the perinuclear area and to the cell membrane of differentiated rat neuronal B104 cells.


Mapping

Gross (2022) mapped the FAM168B gene to chromosome 2q21.1 based on an alignment of the FAM168B sequence (GenBank BC066347) with the genomic sequence (GRCh38).


Gene Function

Mishra et al. (2011) showed that MANI expression was downregulated in brains of patients with Alzheimer disease (AD; 104300), as well as in brains of an AD mouse model. Ectopic expression of human MANI in catecholaminergic PC12 cells induced alterations in phosphorylation and the cleavage pattern of App (104760). Mani was not expressed in mouse neural stem cells (NSCs), but it was expressed in differentiated neurons and promoted their survival. Mani overexpression promoted NSC differentiation and neurogenesis, and it inhibited neurite outgrowth through Stmn2 (600621) and Stat3 (102582) in catecholaminergic PC12 cells. Furthermore, Mani interacted with Cdc27 (116946) to modulate the cell cycle, thereby regulating survival and differentiation of neurons.

Mishra et al. (2012) showed that Mani inhibited neurite outgrowth, as knockdown of Mani in primary rat cortical neurons had significantly longer neurites than controls. A yeast-2-hybrid screen revealed that Mani interacted with several proteins involved in governing neurite outgrowth.


REFERENCES

  1. Gross, M. B. Personal Communication. Baltimore, Md. 10/13/2022.

  2. Mishra, M., Akatsu, H., Heese, K. The novel protein MANI modulates neurogenesis and neurite-cone growth. J. Cell. Molec. Med. 15: 1713-1725, 2011. [PubMed: 20716133] [Full Text: https://doi.org/10.1111/j.1582-4934.2010.01134.x]

  3. Mishra, M., Lee, S., Lin, M. K., Yamashita, T., Heese, K. Characterizing the neurite outgrowth inhibitory effect of Mani. FEBS Lett. 586: 3018-3023, 2012. [PubMed: 22771904] [Full Text: https://doi.org/10.1016/j.febslet.2012.06.043]


Contributors:
Matthew B. Gross - updated : 10/13/2022

Creation Date:
Bao Lige : 10/13/2022

Edit History:
alopez : 10/14/2022
mgross : 10/13/2022