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Diabetes 50:694-696, 2001
© 2001 by the American Diabetes Association, Inc.

Mutations in the Coding Region of the Neurogenin 3 Gene (NEUROG3) Are Not a Common Cause of Maturity-Onset Diabetes of the Young in Japanese Subjects

Laura del Bosque-Plata1,2, Joseph Lin6, Yukio Horikawa1,2, Peter E.H. Schwarz1,2, Nancy J. Cox3,4, Naoko Iwasaki5, Makiko Ogata5, Yasuhiko Iwamoto5, Michael S. German6, and Graeme I. Bell1,2,3,4

1 Howard Hughes Medical Institute and the
2 Departments of Biochemistry and Molecular Biology
3 Medicine, and
4 Human Genetics, the University of Chicago, Chicago, Illinois
5 Diabetes Center, Tokyo Women’s Medical University, Tokyo, Japan
6 Hormone Research Institute and Department of Medicine, University of California San Francisco, San Francisco, California


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 RESEARCH DESIGN AND METHODS
 REFERENCES
 
Mutations in transcription factors that play a role in the development of the endocrine pancreas, such as insulin promoter factor-1 and NeuroD1/BETA2, have been associated with diabetes. Cell type–specific members of the basic helix-loop-helix (bHLH) family of transcription factors play essential roles in the development and maintenance of many differentiated cell types, including pancreatic ß-cells. Neurogenin 3 is a bHLH transcription factor that is expressed in the developing central nervous system and the embryonic pancreas. Mice lacking this transcription factor fail to develop any islet endocrine cells and die postnatally from diabetes. Because neurogenin 3 is required for the development of ß-cells and other pancreatic islet cell types, we considered it a candidate diabetes gene. We screened the coding region of the human neurogenin 3 gene (NEUROG3) for mutations in a group of unrelated Japanese subjects with maturity-onset diabetes of the young (MODY). We found three sequence variants: a deletion of 2-bp in the 5'-untranslated region (NEUROG3-g.-44–45delCA), a G-to-A substitution in codon 167 (g.499G/A), resulting in a Gly-to-Arg replacement (G/R167), and a T-to-C substitution in codon 199 (g.596T/C), resulting in a Phe/Ser polymorphism F/S199. These polymorphisms were not associated with MODY, thereby suggesting that mutations in NEUROG3 are not a common cause of MODY in Japanese patients.

Abbreviations: bHLH, basic helix-loop-helix; HNF, hepatocyte nuclear factor; IPF, insulin promoter factor; MODY, maturity-onset diabetes of the young; PCR, polymerase chain reaction


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
RESEARCH DESIGN AND METHODS
 REFERENCES
 
Heterozygous mutations in transcription factors expressed in the developing endocrine pancreas and/or in mature pancreatic ß-cells have been associated with diabetes (1–5). They include a member of the nuclear receptor superfamily (hepatocyte nuclear factor [HNF]-4{alpha}), homeodomain-containing proteins (HNF-1{alpha} and -1ß and insulin promoter factor [IPF]-1), and a basic helix-loop-helix (bHLH) protein (NeuroD1/BETA2). The cell type–specific (class B) family of bHLH transcription factors, of which NeuroD1 is a member, play essential roles in the development and maintenance of many differentiated cell types, including those of the endocrine pancreas (6,7). The developing pancreas and mature islet cells express a number of class B bHLH transcription factors, including NeuroD1, scleraxis/meso1, mist1, mash1, NeuroD4/math3, and neurogenin 3 (7). Neurogenin 3 appears to be a marker of precursor endocrine cells and is absent from differentiated endocrine cells (7–10). Ectopic expression of neurogenin 3 during early pancreatic development using the Ipf-1/PDX promoter results in precocious differentiation of pancreatic precursor cells into endocrine cells, and mice lacking neurogenin 3 fail to generate any pancreatic endocrine cells and die postnatally from diabetes. Because neurogenin 3 appears to be a positive regulator of pancreatic endocrine development, we proposed that genetic variation in this gene could affect ß-cell mass or the ability of the ß-cell to compensate for insulin resistance, thereby leading to diabetes. To test this hypothesis, we screened a group of subjects with maturity-onset diabetes of the young (MODY), a form of diabetes characterized by ß-cell and/or islet dysfunction (1–5,11), for mutations in the neurogenin 3 gene, NEUROG3.

NEUROG3 consists of one exon, the complete sequence of which has been determined (GenBank accession nos. AJ133776 and AF234829; the latter sequence is also available in an online appendix [Fig. A1] at www.diabetes.org/diabetes/appendix.asp). Physical mapping using the G3 Radiation Hybrid Mapping Panel (Research Genetics, Huntsville, AL) localized NEUROG3 to a region 92.2 cM from pter near the anonymous DNA marker D10S1665 (logarithm of odds [LOD] score = 5.54; 48 cRs) in chromosome bands 10q21.2–q21.3. Thus, D10S1665 can be used as a marker for NEUROG3 in linkage studies.

We screened the coding region of NEUROG3 for mutations in a group of 57 unrelated Japanese subjects with MODY. We found three sequence variants (Table 1): an uncommon 2-bp deletion in the 5'-untranslated region (NEUROG3-g.-44–45delCA), a low frequency G-to-A substitution in codon 167 (g.499G/A), resulting in a Gly-to-Arg replacement (G/R167), and a common C-to-T substitution in codon 199 (g.596T/C), resulting in a Phe/Ser amino acid polymorphism (F/S199). These polymorphisms were also found in Japanese subjects with type 2 diabetes and in Europeans of German ancestry (Table 1). There is no evidence that these polymorphisms are either pathogenic or the cause of MODY in our Japanese subjects. The two amino acid substitutions that we found (G/R167 and F/S199) are located in the COOH-terminal region of neurogenin 3 following the DNA-binding bHLH domain. Both amino acid substitutions are nonconservative and affect residues that are conserved among the human, mouse, and rat sequences (Fig. A2 at www.diabetes.org/diabetes/appendix.asp). Their effect on neurogenin 3 function remains to be determined.


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  		Table 1 Polymorphisms in NEUROG3

 
In conclusion, we have described three polymorphisms in the proendocrine gene NEUROG3. Direct screening for mutations and association studies suggest that mutations in the coding region of NEUROG3 are unlikely to be a major cause of MODY in Japan. However, because MODY is a heterogeneous disorder and mutations in another member of the bHLH family of transcription factors involved in development and maturation of pancreatic ß-cells (NEUROD1) can cause MODY (5), there may be rare families with diabetes attributable to mutations in NEUROG3.


   RESEARCH DESIGN AND METHODS
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
REFERENCES
 
Study population.
The study population consisted of 57 unrelated Japanese subjects with a diagnosis of MODY, the clinical features of which have been described previously (12). These subjects have previously been screened for mutations in the HNF-1{alpha}, -1ß, -4{alpha}, and -3ß genes and the DCoH, IPF-1, NeuroD1/BETA2, and Nkx2.2 genes (13). Mutations in the HNF-1{alpha} gene have been excluded as the cause of MODY in each of these subjects. However, this group does include one subject with a nonsense mutation in the HNF-1ß gene (2) and two subjects with putative diabetes-associated mutations in the HNF-4{alpha} gene (14).

Screening for mutations in NEUROG3.
The coding region was screened for mutations by amplifying specific regions using the primers shown in Table 2 and then directly sequencing the PCR products using an ABI PRISM dRhodamine terminator cycle sequencing ready reaction kit (Applied Biosystems, Foster City, CA). The polymorphisms were typed in groups of unrelated nondiabetic and type 2 diabetic Japanese subjects and a random sample of German subjects by DNA sequencing.


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  		Table 2 Sequences of primers for amplification and sequencing of NEUROG3

 


   ACKNOWLEDGMENTS
 
This study was supported by the Howard Hughes Medical Institute, the Blum-Kovler Foundation, and grants from the U.S. Public Health Service (DK-20595, DK-44840, DK-48281, and DK-21344), the Nora Eccles Treadwell Foundation, the Japanese Ministry of Health and Welfare (for Research on Human Genome and Gene Therapy), the Japanese Ministry of Science, Culture and Sport (10671084), the Uehara Memorial Foundation, and the Naito Memorial Foundation.


   FOOTNOTES
 
Address correspondence and reprint requests to Graeme Bell, Howard Hughes Medical Institute, the University of Chicago, 5841 South Maryland Ave., MC1028, Chicago, IL 60637. E-mail: g-bell{at}uchicago.edu.

Received for publication 7 March 2000 and accepted in revised form 22 November 2000.

Additional information can be found in an online appendix at www.diabetes.org/diabetes/appendix.asp.


   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 REFERENCES
 

  1. Yamagata K, Oda N, Kaisaki PJ, Menzel S, Furuta H, Vaxillaire M, Southam L, Cox RD, Lathrop GM, Boriraj VV, Chen X, Cox NJ, Oda Y, Yano H, Le Beau MM, Yamada S, Nishigori H, Takeda J, Fajans SS, Hattersley AT, Iwasaki N, Hansen T, Pedersen O, Polonsky KS, Turner RC, Velho G, Chèvre J-C, Froguel P, Bell GI: Mutations in the hepatocyte nuclear factor-1{alpha} gene in maturity-onset diabetes of the young (MODY3). Nature 384:455–458, 1996[Medline]
  2. Horikawa Y, Iwasaki N, Hara M, Furuta H, Hinokio Y, Cockburn BN, Lindner T, Yamagata K, Ogata M, Tomonaga O, Kuroki H, Kasahara T, Iwamoto Y, Bell GI: Mutation in hepatocyte nuclear factor-1ß gene (TCF2) associated with MODY. Nat Genet 17:384–385, 1997[Medline]
  3. Yamagata K, Furuta H, Oda N, Kaisaki PJ, Menzel S, Cox NJ, Fajans SS, Signorini S, Stoffel M, Bell GI: Mutations in the hepatocyte nuclear factor-4{alpha} gene in maturity-onset diabetes of the young (MODY1). Nature 384:458–460, 1996[Medline]
  4. Stoffers DA, Ferrer J, Clarke WL, Habener JF: Early-onset type-II diabetes mellitus (MODY4) linked to IPF1. Nat Genet 17:138–139, 1997[Medline]
  5. Malecki MT, Jhala US, Antonellis A, Fields L, Doria A, Orban T, Saad M, Warram JH, Montminy M, Krolewski AS: Mutations in NEUROD1 are associated with the development of type 2 diabetes. Nat Genet 23:323–328, 1999[Medline]
  6. Littlewood T, Ewan GI: Helix-Loop-Helix Transcription Factors . 3rd ed. Oxford, Oxford University Press, 1998
  7. Schwitzgebel VM, Scheel DW, Conners JR, Kalamaras J, Lee JE, Anderson DJ, Sussel L, Johnson JD, German MS: Expression of neurogenin3 reveals an islet cell precursor population in the pancreas. Development 127:3533–3542, 2000[Abstract]
  8. Apelqvist A, Li H, Sommer L, Beatus P, Anderson DJ, Honjo T, Hrabe de Angelis M, Lendahl U, Edlund H: Notch signalling controls pancreatic cell differentiation. Nature 400:877–881, 1999[Medline]
  9. Jensen J, Heller RS, Funder-Nielsen T, Pedersen EE, Lindsell C, Weinmaster G, Madsen O, Serup P: Independent development of pancreatic {alpha}- and ß-cells from neurogenin3-expressing precursors: a role for the notch pathway in repression of premature differentiation. Diabetes 49:163–176, 2000[Abstract]
  10. Gradwohl G, Dierich A, LeMeur M, Guillemot F: neurogenin3 is required for the development of the four endocrine cell lineages of the pancreas. Proc Natl Acad Sci U S A 97:1607–1611, 2000[Abstract/Free Full Text]
  11. Ilag LL, Tabaei BP, Herman WH, Zawacki CM, D’Souza E, Bell GI, Fajans SS: Reduced pancreatic polypeptide response to hypoglycemia and amylin response to arginine in subjects with a mutation in the HNF-4{alpha}/MODY1 gene. Diabetes 49:961–968, 2000[Abstract]
  12. Furuta H, Horikawa Y, Iwasaki N, Hara M, Sussel L, Le Beau MM, Davis EM, Ogata M, Iwamoto Y, German MS, Bell GI: ß-cell transcription factors and diabetes: mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese. Diabetes 47:1356–1358, 1998[Medline]
  13. Hinokio Y, Horikawa Y, Furuta H, Cox NJ, Iwasaki N, Honda M, Ogata M, Iwamoto Y, Bell GI: ß-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3ß gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young. Diabetes 49:302–305, 2000[Abstract]
  14. Furuta H, Iwasaki N, Oda N, Hinokio Y, Horikawa Y, Yamagata K, Yano N, Sugahiro J, Ogata M, Ohgwara H, Omori Y, Iwamoto Y, Bell GI: Organization and partial sequence of the hepatocyte nuclear factor-4{alpha}/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY. Diabetes 46:1652–1657, 1997[Abstract]
  15. Antonarakis SE: Recommendations for a nomenclature system for human gene mutations: Nomenclature Working Group. Hum Mutat 11:1–3, 1998

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