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{{Short description|Protein-coding gene in the species Homo sapiens}}
{{Infobox_gene}}
{{Infobox_gene}}
'''Myosin regulatory light chain interacting protein''', also known as '''MYLIP''', is a [[protein]] that in humans is encoded by the ''MYLIP'' [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: MYLIP myosin regulatory light chain interacting protein| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=29116| accessdate = }}</ref>
'''Myosin regulatory light chain interacting protein''', also known as '''MYLIP''', is a [[protein]] that in humans is encoded by the ''MYLIP'' [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: MYLIP myosin regulatory light chain interacting protein| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=29116}}</ref>


MYLIP is also known as IDOL "Inducible Degrader of the LDL receptor" based on its involvement in cholesterol regulation.<ref name="pmid19520913">{{cite journal |vauthors=Zelcer N, Hong C, Boyadjian R, Tontonoz P | title = LXR regulates cholesterol uptake through Idol-dependent ubiquitination of the LDL receptor | journal = Science | volume = 325 | issue = 5936 | pages = 100–4 |date=July 2009 | pmid = 19520913 | doi = 10.1126/science.1168974 | url = | issn = | pmc = 2777523 }}</ref><ref name="pmid19688294">{{cite journal |vauthors=Lindholm D, Bornhauser BC, Korhonen L | title = Mylip makes an Idol turn into regulation of LDL receptor | journal = Cell. Mol. Life Sci. | volume = 66 | issue = 21 | pages = 3399–402 |date=November 2009 | pmid = 19688294 | doi = 10.1007/s00018-009-0127-y | url = | issn = }}</ref> The expression of IDOL is induced by the sterol-activated [[liver X receptor]].
MYLIP is also known as IDOL "Inducible Degrader of the LDL receptor" based on its involvement in cholesterol regulation or MIR "Modulator Of Immune Recognition".<ref name="pmid19520913">{{cite journal |vauthors=Zelcer N, Hong C, Boyadjian R, Tontonoz P | title = LXR regulates cholesterol uptake through Idol-dependent ubiquitination of the LDL receptor | journal = Science | volume = 325 | issue = 5936 | pages = 100–4 |date=July 2009 | pmid = 19520913 | doi = 10.1126/science.1168974 | pmc = 2777523 | bibcode = 2009Sci...325..100Z }}</ref><ref name="pmid19688294">{{cite journal |vauthors=Lindholm D, Bornhauser BC, Korhonen L | title = Mylip makes an Idol turn into regulation of LDL receptor | journal = Cell. Mol. Life Sci. | volume = 66 | issue = 21 | pages = 3399–402 |date=November 2009 | pmid = 19688294 | doi = 10.1007/s00018-009-0127-y | s2cid = 34153384 | pmc = 11115883 }}</ref> The expression of IDOL is induced by the sterol-activated [[liver X receptor]].


'''Increased Degradation of LDL Receptor Protein''' (IDOL) is a ubiquitin ligase that ubiquinates LDL receptors in endosomes and directs the receptors to the lysosomal compartment for degradation. IDOL is transcriptionally up-regulated by LXR/RXR in response to an increase in intracellular cholesterol.<ref>{{cite journal | author = Sawamura, T. | title = New Idol for cholesterol reduction? | journal = Clin. Chem. | volume = 55 | issue = 12| pages = 2082–2084 |date= 2009 | pmid = | doi = 10.1373/clinchem.2009.134023 | url = | issn = }}</ref> Pharmacologic inhibition of IDOL could reduce plasma LDL cholesterol by increasing plasma LDL receptor density.
'''Increased Degradation of LDL Receptor Protein''' (IDOL) is a [[ubiquitin]] ligase that ubiquinates LDL receptors in endosomes and directs the receptors to the lysosomal compartment for degradation. IDOL is transcriptionally up-regulated by LXR/RXR in response to an increase in intracellular cholesterol.<ref>{{cite journal | author = Sawamura, T. | title = New Idol for cholesterol reduction? | journal = Clin. Chem. | volume = 55 | issue = 12| pages = 2082–2084 |date= 2009 | pmid = 19833835| doi = 10.1373/clinchem.2009.134023 | doi-access = free }}</ref> Pharmacologic inhibition of IDOL could reduce plasma LDL cholesterol by increasing plasma LDL receptor density.


== Function ==
== Function ==
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==Further reading==
==Further reading==
{{refbegin | 2}}
{{refbegin | 2}}
*{{cite journal |vauthors=Olsson PA, Korhonen L, Mercer EA, Lindholm D |title=MIR is a novel ERM-like protein that interacts with myosin regulatory light chain and inhibits neurite outgrowth. |journal=J. Biol. Chem. |volume=274 |issue= 51 |pages= 36288–92 |year= 2000 |pmid= 10593918 |doi=10.1074/jbc.274.51.36288 |doi-access=free }}
{{PBB_Further_reading
| citations =
*{{cite journal |vauthors=Olsson PA, Korhonen L, Mercer EA, Lindholm D |title=MIR is a novel ERM-like protein that interacts with myosin regulatory light chain and inhibits neurite outgrowth. |journal=J. Biol. Chem. |volume=274 |issue= 51 |pages= 36288–92 |year= 2000 |pmid= 10593918 |doi=10.1074/jbc.274.51.36288 }}
*{{cite journal |vauthors=Zhang QH, Ye M, Wu XY, etal |title=Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells. |journal=Genome Res. |volume=10 |issue= 10 |pages= 1546–60 |year= 2001 |pmid= 11042152 |doi=10.1101/gr.140200 | pmc=310934 }}
*{{cite journal |vauthors=Zhang QH, Ye M, Wu XY, etal |title=Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells. |journal=Genome Res. |volume=10 |issue= 10 |pages= 1546–60 |year= 2001 |pmid= 11042152 |doi=10.1101/gr.140200 | pmc=310934 }}
*{{cite journal |vauthors=Olsson PA, Bornhauser BC, Korhonen L, Lindholm D |title=Neuronal expression of the ERM-like protein MIR in rat brain and its localization to human chromosome 6. |journal=Biochem. Biophys. Res. Commun. |volume=279 |issue= 3 |pages= 879–83 |year= 2001 |pmid= 11162443 |doi= 10.1006/bbrc.2000.4028 }}
*{{cite journal |vauthors=Olsson PA, Bornhauser BC, Korhonen L, Lindholm D |title=Neuronal expression of the ERM-like protein MIR in rat brain and its localization to human chromosome 6. |journal=Biochem. Biophys. Res. Commun. |volume=279 |issue= 3 |pages= 879–83 |year= 2001 |pmid= 11162443 |doi= 10.1006/bbrc.2000.4028 }}
*{{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 }}
*{{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |bibcode=2002PNAS...9916899M |doi-access=free }}
*{{cite journal |vauthors=Bornhauser BC, Olsson PA, Lindholm D |title=MSAP is a novel MIR-interacting protein that enhances neurite outgrowth and increases myosin regulatory light chain. |journal=J. Biol. Chem. |volume=278 |issue= 37 |pages= 35412–20 |year= 2003 |pmid= 12826659 |doi= 10.1074/jbc.M306271200 }}
*{{cite journal |vauthors=Bornhauser BC, Olsson PA, Lindholm D |title=MSAP is a novel MIR-interacting protein that enhances neurite outgrowth and increases myosin regulatory light chain. |journal=J. Biol. Chem. |volume=278 |issue= 37 |pages= 35412–20 |year= 2003 |pmid= 12826659 |doi= 10.1074/jbc.M306271200 |doi-access= free }}
*{{cite journal |vauthors=Bornhauser BC, Johansson C, Lindholm D |title=Functional activities and cellular localization of the ezrin, radixin, moesin (ERM) and RING zinc finger domains in MIR. |journal=FEBS Lett. |volume=553 |issue= 1-2 |pages= 195–9 |year= 2003 |pmid= 14550572 |doi=10.1016/S0014-5793(03)01010-X }}
*{{cite journal |vauthors=Bornhauser BC, Johansson C, Lindholm D |title=Functional activities and cellular localization of the ezrin, radixin, moesin (ERM) and RING zinc finger domains in MIR. |journal=FEBS Lett. |volume=553 |issue= 1–2 |pages= 195–9 |year= 2003 |pmid= 14550572 |doi=10.1016/S0014-5793(03)01010-X |s2cid=25599548 |doi-access=free }}
*{{cite journal |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }}
*{{cite journal |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }}
*{{cite journal |vauthors=Wan D, Gong Y, Qin W, etal |title=Large-scale cDNA transfection screening for genes related to cancer development and progression. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 44 |pages= 15724–9 |year= 2004 |pmid= 15498874 |doi= 10.1073/pnas.0404089101 | pmc=524842 }}
*{{cite journal |vauthors=Wan D, Gong Y, Qin W, etal |title=Large-scale cDNA transfection screening for genes related to cancer development and progression. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 44 |pages= 15724–9 |year= 2004 |pmid= 15498874 |doi= 10.1073/pnas.0404089101 | pmc=524842 |bibcode=2004PNAS..10115724W |doi-access=free }}
*{{cite journal |vauthors=Rual JF, Venkatesan K, Hao T, etal |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 }}
*{{cite journal |vauthors=Rual JF, Venkatesan K, Hao T, etal |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 |bibcode=2005Natur.437.1173R |s2cid=4427026 }}
*{{cite journal |vauthors=Ohmura-Hoshino M, Matsuki Y, Aoki M, etal |title=Inhibition of MHC class II expression and immune responses by c-MIR. |journal=J. Immunol. |volume=177 |issue= 1 |pages= 341–54 |year= 2006 |pmid= 16785530 |doi= 10.4049/jimmunol.177.1.341}}
*{{cite journal |vauthors=Ohmura-Hoshino M, Matsuki Y, Aoki M, etal |title=Inhibition of MHC class II expression and immune responses by c-MIR. |journal=J. Immunol. |volume=177 |issue= 1 |pages= 341–54 |year= 2006 |pmid= 16785530 |doi= 10.4049/jimmunol.177.1.341|doi-access=free }}
}}
{{refend}}
{{refend}}


{{Cytoskeletal proteins}}{{gene-6-stub}}


{{gene-6-stub}}

Latest revision as of 06:10, 27 May 2024

MYLIP
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMYLIP, IDOL, MIR, myosin regulatory light chain interacting protein
External IDsOMIM: 610082; MGI: 2388271; HomoloGene: 8309; GeneCards: MYLIP; OMA:MYLIP - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_013262

NM_153789

RefSeq (protein)

NP_037394

NP_722484

Location (UCSC)Chr 6: 16.13 – 16.15 MbChr 13: 45.54 – 45.57 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Myosin regulatory light chain interacting protein, also known as MYLIP, is a protein that in humans is encoded by the MYLIP gene.[5]

MYLIP is also known as IDOL "Inducible Degrader of the LDL receptor" based on its involvement in cholesterol regulation or MIR "Modulator Of Immune Recognition".[6][7] The expression of IDOL is induced by the sterol-activated liver X receptor.

Increased Degradation of LDL Receptor Protein (IDOL) is a ubiquitin ligase that ubiquinates LDL receptors in endosomes and directs the receptors to the lysosomal compartment for degradation. IDOL is transcriptionally up-regulated by LXR/RXR in response to an increase in intracellular cholesterol.[8] Pharmacologic inhibition of IDOL could reduce plasma LDL cholesterol by increasing plasma LDL receptor density.

Function

[edit]

The ERM protein family members ezrin, radixin, and moesin are cytoskeletal effector proteins linking actin to membrane-bound proteins at the cell surface. Myosin regulatory light chain interacting protein (MYLIP) is a novel ERM-like protein that interacts with myosin regulatory light chain and inhibits neurite outgrowth.[5]

References

[edit]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000007944Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000038175Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: MYLIP myosin regulatory light chain interacting protein".
  6. ^ Zelcer N, Hong C, Boyadjian R, Tontonoz P (July 2009). "LXR regulates cholesterol uptake through Idol-dependent ubiquitination of the LDL receptor". Science. 325 (5936): 100–4. Bibcode:2009Sci...325..100Z. doi:10.1126/science.1168974. PMC 2777523. PMID 19520913.
  7. ^ Lindholm D, Bornhauser BC, Korhonen L (November 2009). "Mylip makes an Idol turn into regulation of LDL receptor". Cell. Mol. Life Sci. 66 (21): 3399–402. doi:10.1007/s00018-009-0127-y. PMC 11115883. PMID 19688294. S2CID 34153384.
  8. ^ Sawamura, T. (2009). "New Idol for cholesterol reduction?". Clin. Chem. 55 (12): 2082–2084. doi:10.1373/clinchem.2009.134023. PMID 19833835.

Further reading

[edit]