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Polyglutamine tract

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synthesis. It is believed that cells cannot properly dispose of proteins with overlong polyglutamine tracts, which over time leads to damage in
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of such a gene often have different numbers of triplets since the highly repetitive sequence is prone to contraction and expansion.
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Wharton KA, Yedvobnick B, Finnerty VG, Artavanis-Tsakonas S (1985). "opa: a novel family of transcribed repeats shared by the
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defects. The significance of similarly expanded tracts in humans became evident when polyQ tracts were found to underlie
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causes a polyglutamine tract in a specific gene to become too long. Important examples of polyglutamine diseases are
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into a protein, each of these triplets gives rise to a glutamine unit, resulting in a polyglutamine tract. Different
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cell can lead to children that are more affected or display an earlier onset and greater severity of the condition.
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Nucleotide sequences encoding a lengthy polyQ tract were first noted in the gene encoding the
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polyQ tract, as caused by triplet repeat instability, was later found to cause
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units. A tract typically consists of about 10 to a few hundred such units.
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Polyglutamine Diseases: A Devastating Genetic Stutter
307: 259:locus and other developmentally regulated loci in 363: 308:Rice C, Beekman D, Liu L, Erives A (2015). 301: 182:Usdin K, House NC, Freudenreich CH (2015). 175: 248: 341: 207: 16:Protein region with only glutamine units 364: 109:is considered to be a consequence of 31:consisting of a sequence of several 13: 137:. Variation of the length of this 14: 388: 243:Howard Hughes Medical Institute 224: 107:Trinucleotide repeat expansion 99:Trinucleotide repeat expansion 1: 245:. Retrieved 30 December 2008. 188:Crit. Rev. Biochem. Mol. Biol 168: 322:G3: Genes, Genomes, Genetics 279:10.1016/0092-8674(85)90308-3 200:10.3109/10409238.2014.999192 159:nucleotide repeat expansions 7: 155:neurodegenerative disorders 79:neurodegenerative disorders 10: 393: 128: 111:slipped strand mispairing 101:occurring in a parental 151:spinocerebellar ataxias 157:were found to involve 153:. In general, several 91:spinocerebellar ataxia 83:polyglutamine diseases 334:10.1534/g3.115.021659 147:Huntington's disease 95:Huntington's disease 77:Several inheritable 66:. When the gene is 21:polyglutamine tract 237:2013-05-07 at the 165:coding sequences. 27:is a portion of a 372:Peptide sequences 328:(15): 2405–2419. 384: 356: 355: 345: 305: 299: 298: 252: 246: 228: 222: 221: 211: 179: 392: 391: 387: 386: 385: 383: 382: 381: 362: 361: 360: 359: 306: 302: 262:D. melanogaster 253: 249: 239:Wayback Machine 230:Laura Bonetta, 229: 225: 180: 176: 171: 131: 115:DNA replication 38:A multitude of 17: 12: 11: 5: 390: 380: 379: 374: 358: 357: 300: 247: 223: 173: 172: 170: 167: 135:Notch receptor 130: 127: 113:either during 15: 9: 6: 4: 3: 2: 389: 378: 375: 373: 370: 369: 367: 353: 349: 344: 339: 335: 331: 327: 323: 319: 317: 313: 304: 296: 292: 288: 284: 280: 276: 272: 268: 264: 263: 258: 251: 244: 240: 236: 233: 227: 219: 215: 210: 205: 201: 197: 194:(2): 142–67. 193: 189: 185: 178: 174: 166: 164: 160: 156: 152: 148: 144: 143:developmental 140: 136: 126: 124: 120: 116: 112: 108: 104: 100: 96: 92: 88: 85:, occur if a 84: 80: 75: 73: 69: 65: 62: 59: 55: 52: 49: 45: 41: 36: 34: 30: 26: 22: 325: 321: 315: 311: 303: 273:(1): 55–62. 270: 266: 260: 256: 250: 226: 191: 187: 177: 149:and several 132: 76: 37: 24: 20: 18: 123:nerve cells 25:polyQ tract 366:Categories 316:Drosophila 169:References 119:DNA repair 68:translated 44:nucleotide 33:glutamine 377:Mutation 352:26362765 235:Archived 218:25608779 103:germline 87:mutation 46:triplet 343:4632060 295:9951524 287:2981631 209:4454471 163:protein 129:History 72:alleles 29:protein 350:  340:  293:  285:  216:  206:  81:, the 312:Notch 291:S2CID 257:Notch 139:Notch 40:genes 348:PMID 283:PMID 267:Cell 214:PMID 93:and 338:PMC 330:doi 314:in 275:doi 265:". 204:PMC 196:doi 161:in 117:or 97:. 56:or 23:or 368:: 346:. 336:. 324:. 320:. 289:. 281:. 271:40 269:. 241:, 212:. 202:. 192:50 190:. 186:. 19:A 354:. 332:: 326:5 318:" 297:. 277:: 220:. 198:: 64:A 61:A 58:C 54:G 51:A 48:C

Index

protein
glutamine
genes
nucleotide
C
A
G
C
A
A
translated
alleles
neurodegenerative disorders
polyglutamine diseases
mutation
spinocerebellar ataxia
Huntington's disease
Trinucleotide repeat expansion
germline
Trinucleotide repeat expansion
slipped strand mispairing
DNA replication
DNA repair
nerve cells
Notch receptor
Notch
developmental
Huntington's disease
spinocerebellar ataxias
neurodegenerative disorders

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