Localization and expression of usherin: a novel basement membrane protein defective in people with Usher's syndrome-type IIa

被引:60
|
作者
Bhattacharya, G
Miller, C
Kimberling, WJ
Jablonski, MM
Cosgrove, D
机构
[1] Boys Town Natl Res Hosp, Omaha, NE 68131 USA
[2] Univ Tennessee, Memphis, TN 38163 USA
关键词
Usher's syndrome; usherin; basement membrane; cochlea; retinitis pigmentosa;
D O I
10.1016/S0378-5955(01)00344-6
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
People with Usher's syndrome type IIa have mutations in a novel gene encoding a protein with domains commonly found in many types of extracellular matrix and cell surface receptor proteins. Here we report that this protein, which we refer to as usherin, is a new basement membrane protein. In the mouse, usherin has a broad, but not ubiquitous, tissue distribution. Usherin is found in all of the capillary and structural basement membranes of the human and mouse retina and in the murine inner ear at both post-natal day 0 and in the adult. High levels of usherin are also observed. in tissues not affected in Usher's syndrome type IIa, including spleen, testis, oviduct, epididymis, submaxillary gland, and large and small intestines. Many organs are completely devoid of usherin, including the brain, skin, kidney, lung, liver, and skeletal muscle. Expression was observed in the smooth muscle of the small intestine, colon, and oviduct, however, usherin is not present in cardiac smooth muscle. Usherin is critical for normal development and tissue homeostasis in the inner ear and retina, illustrating yet another example of the importance of basement membranes in the development and function of tissues. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1 / 11
页数:11
相关论文
共 8 条
  • [1] Expression, distribution, and integration of usherin: a novel basement membrane protein defective in people with Usher syndrome type IIa.
    Cosgrove, DE
    Bhattacharia, G
    Kalluri, R
    Kimberling, WJ
    Jablonski, MM
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2001, 42 (04) : S654 - S654
  • [2] Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells
    Adato, A
    Lefèvre, G
    Delprat, B
    Michel, V
    Michalski, N
    Chardenoux, S
    Weil, D
    El-Amraoui, A
    Petit, C
    HUMAN MOLECULAR GENETICS, 2005, 14 (24) : 3921 - 3932
  • [3] Genomic structure and identification of novel mutations in Usherin, the gene responsible for Usher syndrome type IIa
    Weston, MD
    Eudy, JD
    Fujita, S
    Yao, SF
    Usami, S
    Cremers, C
    Greenburg, J
    Ramesar, R
    Martini, A
    Moller, C
    Smith, RJ
    Sumegi, J
    Kimberling, WJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (04) : 1199 - 1210
  • [5] X-linked Alport Syndrome with Type IV Collagen α5 Chain Staining Revealing Normal Expression in the Glomerular Basement Membrane and Negative on Bowman's Capsule and Distal Tubular Basement Membrane: A Case Report
    Okamoto, Takuya
    Shima, Hisato
    Doi, Toshio
    Nozu, Kandai
    Inoue, Tomoko
    Tashiro, Manabu
    Wariishi, Seiichiro
    Bando, Hiroyasu
    Azuma, Hiroyuki
    Iwasaka, Naohito
    Ohara, Takuji
    Okada, Kazuyoshi
    Minakuchi, Jun
    TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 2023, 261 (01): : 69 - 73
  • [6] Ezrin Is a Novel Protein Partner of Aquaporin-5 in Human Salivary Glands and Shows Altered Expression and Cellular Localization in Sjogren's Syndrome
    Chivasso, Clara
    Hagstromer, Carl Johan
    Rose, Kristie L.
    Lhotellerie, Florent
    Leblanc, Lionel
    Wang, Zhen
    Moscato, Stefania
    Chevalier, Clement
    Zindy, Egor
    Martin, Maud
    Vanhollebeke, Benoit
    Gregoire, Francoise
    Bolaky, Nargis
    Perret, Jason
    Baldini, Chiara
    Soyfoo, Muhammad Shahnawaz
    Mattii, Letizia
    Schey, Kevin L.
    Tornroth-Horsefield, Susanna
    Delporte, Christine
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (17)
  • [7] Fcγ receptor IIB-deficient mice develop Goodpasture's syndrome upon immunization with type IV collagen:: A novel murine model for autoimmune glomerular basement membrane disease
    Nakamura, A
    Yuasa, T
    Ujike, A
    Ono, M
    Nukiwa, T
    Ravetch, JV
    Takai, T
    JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (05): : 899 - 905
  • [8] Novel lacrimal basement membrane (BM) protein, 'BM180', involved in stimulated secretion displays sequence and immunological similarity with alpha-gliadin: Significance of auto-antigliadin antibodies in Sjogren's syndrome and Celiac disease?
    Laurie, GW
    Ciclitira, PJ
    Ellis, HJ
    Pogany, G
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1996, 37 (03) : 3957 - 3957