SF3A2
SF3A2 (Splicing factor 3a subunit 2) هوَ بروتين يُشَفر بواسطة جين SF3A2 في الإنسان.[1][2][3]
الوظيفة
![[أيقونة]](https://infokontak.com/ar/%D9%85%D9%84%D9%81:Crystal_xedit.svg){kind=small} | هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
الأهمية السريرية
| هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
المراجع
- ^ "Entrez Gene: SF3A2 splicing factor 3a, subunit 2, 66kDa". مؤرشف من الأصل في 2010-12-05.
- ^ Bennett M، Reed R (أكتوبر 1993). "Correspondence between a mammalian spliceosome component and an essential yeast splicing factor". Science. ج. 262 ع. 5130: 105–8. DOI:10.1126/science.8211113. PMID:8211113.
- ^ Dresser DW، Hacker A، Lovell-Badge R، Guerrier D (سبتمبر 1995). "The genes for a spliceosome protein (SAP62) and the anti-Müllerian hormone (AMH) are contiguous". Human Molecular Genetics. ج. 4 ع. 9: 1613–8. DOI:10.1093/hmg/4.9.1613. PMID:8541848.
قراءة متعمقة
- Chiara MD، Champion-Arnaud P، Buvoli M، Nadal-Ginard B، Reed R (يوليو 1994). "Specific protein-protein interactions between the essential mammalian spliceosome-associated proteins SAP 61 and SAP 114". Proceedings of the National Academy of Sciences of the United States of America. ج. 91 ع. 14: 6403–7. DOI:10.1073/pnas.91.14.6403. PMC:44210. PMID:8022796.
- Rain JC، Tartakoff AM، Krämer A، Legrain P (يونيو 1996). "Essential domains of the PRP21 splicing factor are implicated in the binding to PRP9 and PRP11 proteins and are conserved through evolution". Rna. ج. 2 ع. 6: 535–50. PMC:1369393. PMID:8718683.
- Hong W، Bennett M، Xiao Y، Feld Kramer R، Wang C، Reed R (يناير 1997). "Association of U2 snRNP with the spliceosomal complex E". Nucleic Acids Research. ج. 25 ع. 2: 354–61. DOI:10.1093/nar/25.2.354. PMC:146436. PMID:9016565.
- Moraitou M، Patrinou-Georgoula M، Guialis A (مايو 1998). "Structural/functional properties of a mammalian multi-component structure containing all major spliceosomal small nuclear ribonucleoprotein particles". The Biochemical Journal. 332 ( Pt 1) ع. 1: 135–44. PMC:1219461. PMID:9576861.
- Yan D، Perriman R، Igel H، Howe KJ، Neville M، Ares M (سبتمبر 1998). "CUS2, a yeast homolog of human Tat-SF1, rescues function of misfolded U2 through an unusual RNA recognition motif". Molecular and Cellular Biology. ج. 18 ع. 9: 5000–9. PMC:109085. PMID:9710584.
- Neubauer G، King A، Rappsilber J، Calvio C، Watson M، Ajuh P، Sleeman J، Lamond A، Mann M (سبتمبر 1998). "Mass spectrometry and EST-database searching allows characterization of the multi-protein spliceosome complex". Nature Genetics. ج. 20 ع. 1: 46–50. DOI:10.1038/1700. PMID:9731529.
- Krämer A، Grüter P، Gröning K، Kastner B (يونيو 1999). "Combined biochemical and electron microscopic analyses reveal the architecture of the mammalian U2 snRNP". The Journal of Cell Biology. ج. 145 ع. 7: 1355–68. DOI:10.1083/jcb.145.7.1355. PMC:2133165. PMID:10385517.
- Das R، Zhou Z، Reed R (مايو 2000). "Functional association of U2 snRNP with the ATP-independent spliceosomal complex E". Molecular Cell. ج. 5 ع. 5: 779–87. DOI:10.1016/S1097-2765(00)80318-4. PMID:10882114.
- Will CL، Schneider C، MacMillan AM، Katopodis NF، Neubauer G، Wilm M، Lührmann R، Query CC (أغسطس 2001). "A novel U2 and U11/U12 snRNP protein that associates with the pre-mRNA branch site". The EMBO Journal. ج. 20 ع. 16: 4536–46. DOI:10.1093/emboj/20.16.4536. PMC:125580. PMID:11500380.
- Nesic D، Krämer A (أكتوبر 2001). "Domains in human splicing factors SF3a60 and SF3a66 required for binding to SF3a120, assembly of the 17S U2 snRNP, and prespliceosome formation". Molecular and Cellular Biology. ج. 21 ع. 19: 6406–17. DOI:10.1128/MCB.21.19.6406-6417.2001. PMC:99788. PMID:11533230.
- Dresser DW، Jamin SP، Atkins CJ، Guerrier D (أكتوبر 2001). "An expressed GNRP-like gene shares a bi-directional promoter with SF3A2 (SAP62) immediately upstream of AMH". Gene. ج. 277 ع. 1–2: 163–73. DOI:10.1016/S0378-1119(01)00690-4. PMID:11602354.
- Jurica MS، Licklider LJ، Gygi SR، Grigorieff N، Moore MJ (أبريل 2002). "Purification and characterization of native spliceosomes suitable for three-dimensional structural analysis". Rna. ج. 8 ع. 4: 426–39. DOI:10.1017/S1355838202021088. PMC:1370266. PMID:11991638.
- Will CL، Urlaub H، Achsel T، Gentzel M، Wilm M، Lührmann R (سبتمبر 2002). "Characterization of novel SF3b and 17S U2 snRNP proteins, including a human Prp5p homologue and an SF3b DEAD-box protein". The EMBO Journal. ج. 21 ع. 18: 4978–88. DOI:10.1093/emboj/cdf480. PMC:126279. PMID:12234937.
- Takenaka K، Nakagawa H، Miyamoto S، Miki H (أغسطس 2004). "The pre-mRNA-splicing factor SF3a66 functions as a microtubule-binding and -bundling protein". The Biochemical Journal. ج. 382 ع. Pt 1: 223–30. DOI:10.1042/BJ20040521. PMC:1133934. PMID:15142036.
- Colland F، Jacq X، Trouplin V، Mougin C، Groizeleau C، Hamburger A، Meil A، Wojcik J، Legrain P، Gauthier JM (يوليو 2004). "Functional proteomics mapping of a human signaling pathway". Genome Research. ج. 14 ع. 7: 1324–32. DOI:10.1101/gr.2334104. PMC:442148. PMID:15231748.
- Nesic D، Tanackovic G، Krämer A (سبتمبر 2004). "A role for Cajal bodies in the final steps of U2 snRNP biogenesis". Journal of Cell Science. ج. 117 ع. Pt 19: 4423–33. DOI:10.1242/jcs.01308. PMID:15316075.
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