Collectrin, a homologue of ACE2, its transcriptional control and functional perspectives

Biochemical and Biophysical Research Communications

Volumn 363, Issue 1, 2007, Pages 1-5

  Zhang, Yanling ^a   Wada, Jun ^b  

^a HEBEI MEDICAL UNIVERSITY   (China)

^b OKAYAMA UNIVERSITY   (Japan)

Author keywords

Amino acid transport; Collectrin; Insulin secretion; Primary cilia

Indexed keywords

ANGIOTENSIN CONVERTING ENZYME 2; COLLECTRIN; DIPEPTIDYL CARBOXYPEPTIDASE; MEMBRANE PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID TRANSPORT; EUKARYOTIC FLAGELLUM; HUMAN; INSULIN RELEASE; KIDNEY TUBULE ABSORPTION; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN SECRETION; PROTEIN STRUCTURE; SHORT SURVEY; TISSUE DISTRIBUTION; TRANSCRIPTION REGULATION;

AMINO ACID TRANSPORT SYSTEMS; ANIMALS; COLLECTINS; GENE EXPRESSION REGULATION; HUMANS; KIDNEY; PANCREAS; PEPTIDYL-DIPEPTIDASE A; TRANSCRIPTION, GENETIC;

EID: 34548727320     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.08.136     Document Type: Short Survey

References (32)

1. Burrell L.M., Johnston C.I., Tikellis C., and Cooper M.E. ACE2, a new regulator of the renin-angiotensin system. Trends Endocrinol. Metab. 15 (2004) 166-169
2. Medvedev A.E. Angiotensin-converting enzyme-2 and collectrin-recently discovered homologs of angiotensin-transforming enzyme. Biomed. Khim. 49 (2003) 8-9
3. Donoghue M., Hsieh F., Baronas E., Godbout K., Gosselin M., Stagliano N., Donovan M., Woolf B., Robison K., Jeyaseelan R., Breitbart R.E., and Acton S. A novel angiotensin-converting enzyme-related carboxypeptidase (ACE2) converts angiotensin I to angiotensin 1-9. Circ. Res. 87 (2000) E1-E9
4. Vickers C., Hales P., Kaushik V., Dick L., Gavin J., Tang J., Godbout K., Parsons T., Baronas E., Hsieh F., Acton S., Patane M., Nichols A., and Tummino P. Hydrolysis of biological peptides by human angiotensin-converting enzyme-related carboxypeptidase. J. Biol. Chem. 277 (2002) 14838-14843
5. Zhang H., Wada J., Hida K., Tsuchiyama Y., Hiragushi K., Shikata K., Wang H., Lin S., Kanwar Y.S., and Makino H. Collectrin, a collecting duct-specific transmembrane glycoprotein, is a novel homolog of ACE2 and is developmentally regulated in embryonic kidneys. J. Biol. Chem. 276 (2001) 17132-17139
6. Fukui K., Yang Q., Cao Y., Takahashi N., Hatakeyama H., Wang H., Wada J., Zhang Y., Marselli L., Nammo T., Yoneda K., Onishi M., Higashiyama S., Matsuzawa Y., Gonzalez F.J., Weir G.C., Kasai H., Shimomura I., Miyagawa J., Wollheim C.B., and Yamagata K. The HNF-1 target collectrin controls insulin exocytosis by SNARE complex formation. Cell Metab. 2 (2005) 373-384
7. Akpinar P., Kuwajima S., Krutzfeldt J., and Stoffel M. Tmem27: a cleaved and shed plasma membrane protein that stimulates pancreatic beta cell proliferation. Cell Metab. 2 (2005) 385-397
8. Zhang Y., Wada J., Yasuhara A., Iseda I., Eguchi J., Fukui K., Yang Q., Yamagata K., Hiesberger T., Igarashi P., Zhang H., Wang H., Akagi S., Kanwar Y.S., and Makino H. The Role for HNF-1beta-Targeted Collectrin in Maintenance of Primary Cilia and Cell Polarity in Collecting Duct Cells. PLoS ONE 2 (2007) e414
9. Danilczyk U., Sarao R., Remy C., Benabbas C., Stange G., Richter A., Arya S., Pospisilik J.A., Singer D., Camargo S.M., Makrides V., Ramadan T., Verrey F., Wagner C.A., and Penninger J.M. Essential role for collectrin in renal amino acid transport. Nature 444 (2006) 1088-1091
10. Malakauskas S.M., Quan H., Fields T.A., McCall S.J., Yu M.J., Kourany W.M., Frey C.W., and Le T.H. Aminoaciduria and altered renal expression of luminal amino acid transporters in mice lacking novel gene collectrin. Am. J. Physiol. Renal Physiol. 292 (2007) F533-F544
11. Altschul S.F., Madden T.L., Schaffer A.A., Zhang J., Zhang Z., Miller W., and Lipman D.J. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25 (1997) 3389-3402
12. Vogel G. News focus: betting on cilia. Science 310 (2005) 216-218
13. Wheatley D.N. Primary cilia in normal and pathological tissues. Pathobiology 63 (1995) 222-238
14. Singla V., and Reiter J.F. The primary cilium as the cell's antenna: signaling at a sensory organelle. Science 313 (2006) 629-633
15. Nauli S.M., Alenghat F.J., Luo Y., Williams E., Vassilev P., Li X., Elia A.E., Lu W., Brown E.M., Quinn S.J., Ingber D.E., and Zhou J. Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells. Nat. Genet. 33 (2003) 129-137
16. Yoder B.K., Tousson A., Millican L., Wu J.H., Bugg Jr. C.E., Schafer J.A., and Balkovetz D.F. Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium. Am. J. Physiol. Renal Physiol. 282 (2002) F541-F552
17. Moyer J.H., Lee-Tischler M.J., Kwon H.Y., Schrick J.J., Avner E.D., Sweeney W.E., Godfrey V.L., Cacheiro N.L., Wilkinson J.E., and Woychik R.P. Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice. Science 264 (1994) 1329-1333
18. Yamagata K., Oda N., Kaisaki P.J., Menzel S., Furuta H., Vaxillaire M., Southam L., Cox R.D., Lathrop G.M., Boriraj V.V., Chen X., Cox N.J., Oda Y., Yano H., Le Beau M.M., Yamada S., Nishigori H., Takeda J., Fajans S.S., Hattersley A.T., Iwasaki N., Hansen T., Pedersen O., Polonsky K.S., Bell G.I., et al. Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3). Nature 384 (1996) 455-458
19. Horikawa Y., Iwasaki N., Hara M., Furuta H., Hinokio Y., Cockburn B.N., Lindner T., Yamagata K., Ogata M., Tomonaga O., Kuroki H., Kasahara T., Iwamoto Y., and Bell G.I. Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY. Nat. Genet. 17 (1997) 384-385
20. Fajans S.S., Bell G.I., and Polonsky K.S. Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young. N. Engl. J. Med. 345 (2001) 971-980
21. Pontoglio M., Sreenan S., Roe M., Pugh W., Ostrega D., Doyen A., Pick A.J., Baldwin A., Velho G., Froguel P., Levisetti M., Bonner-Weir S., Bell G.I., Yaniv M., and Polonsky K.S. Defective insulin secretion in hepatocyte nuclear factor 1alpha-deficient mice. J. Clin. Invest. 101 (1998) 2215-2222
22. Dukes I.D., Sreenan S., Roe M.W., Levisetti M., Zhou Y.P., Ostrega D., Bell G.I., Pontoglio M., Yaniv M., Philipson L., and Polonsky K.S. Defective pancreatic beta-cell glycolytic signaling in hepatocyte nuclear factor-1alpha-deficient mice. J. Biol. Chem. 273 (1998) 24457-24464
23. Yamagata K., Nammo T., Moriwaki M., Ihara A., Iizuka K., Yang Q., Satoh T., Li M., Uenaka R., Okita K., Iwahashi H., Zhu Q., Cao Y., Imagawa A., Tochino Y., Hanafusa T., Miyagawa J., and Matsuzawa Y. Overexpression of dominant-negative mutant hepatocyte nuclear fctor-1 alpha in pancreatic beta-cells causes abnormal islet architecture with decreased expression of E-cadherin, reduced beta-cell proliferation, and diabetes. Diabetes 51 (2002) 114-123
24. Wang H., Maechler P., Hagenfeldt K.A., and Wollheim C.B. Dominant-negative suppression of HNF-1alpha function results in defective insulin gene transcription and impaired metabolism-secretion coupling in a pancreatic beta-cell line. EMBO J. 17 (1998) 6701-6713
25. Wang H., Antinozzi P.A., Hagenfeldt K.A., Maechler P., and Wollheim C.B. Molecular targets of a human HNF1 alpha mutation responsible for pancreatic beta-cell dysfunction. EMBO J. 19 (2000) 4257-4264
26. Yang Q., Yamagata K., Fukui K., Cao Y., Nammo T., Iwahashi H., Wang H., Matsumura I., Hanafusa T., Bucala R., Wollheim C.B., Miyagawa J., and Matsuzawa Y. Hepatocyte nuclear factor-1alpha modulates pancreatic beta-cell growth by regulating the expression of insulin-like growth factor-1 in INS-1 cells. Diabetes 51 (2002) 1785-1792
27. Orci L. A portrait of the pancreatic B-cell. The Minkowski Award Lecture delivered on July 19, 1973, during the 8th Congress of the International Diabetes Federation, held in Brussels, Belgium. Diabetologia 10 (1974) 163-187
28. Lang J. Molecular mechanisms and regulation of insulin exocytosis as a paradigm of endocrine secretion. Eur. J. Biochem. 259 (1999) 3-17
29. Pontoglio M., Barra J., Hadchouel M., Doyen A., Kress C., Bach J.P., Babinet C., and Yaniv M. Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome. Cell 84 (1996) 575-585
30. Verrey F., Ristic Z., Romeo E., Ramadan T., Makrides V., Dave M.H., Wagner C.A., and Camargo S.M. Novel renal amino acid transporters. Annu. Rev. Physiol. 67 (2005) 557-572
31. Fournier K.M., and Robinson M.B. A dominant-negative variant of SNAP-23 decreases the cell surface expression of the neuronal glutamate transporter EAAC1 by slowing constitutive delivery. Neurochem. Int. 48 (2006) 596-603
32. Hong W. SNAREs and traffic. Biochim. Biophys. Acta 1744 (2005) 120-144