Schnurr Judy A, Storey Kathleen K, Jung Hans-Joachim G, Somers David A, Gronwald John W
Plant Science Research, United States Department of Agriculture-Agricultural Research Services, St. Paul, MN 55108, USA.
Planta. 2006 Aug;224(3):520-32. doi: 10.1007/s00425-006-0240-1. Epub 2006 Mar 24.
Arabidopsis UDP-sugar pyrophosphorylase (AtUSP) is a broad substrate enzyme that synthesizes nucleotide sugars. The products of the AtUSP reaction can act as precursors for the synthesis of glycolipids, glycoproteins, and cell wall components including pectin and hemicellulose. AtUSP has no close homologs in Arabidopsis and its biological function has not been clearly defined. We identified two T-DNA insertional mutant lines for AtUSP, usp-1 and usp-2. No homozygous individuals were identified and progeny from plants heterozygous for usp-1 or usp-2 showed a 1:1 segregation ratio under selection. Despite decreased levels of both AtUSP transcript and USP activity (UDP-GlcA-->GlcA-1-P), heterozygous plants were indistinguishable from wild type at all stages of development. Reciprocal test crosses indicated the source of the segregation distortion was lack of transmission through the male gametophyte. Analysis of pollen tetrads from usp-1 in the quartet background revealed a 2:2 ratio of normal:collapsed pollen grains. The collapsed pollen grains were not viable as determined by Alexander's viability and DAPI staining, and pollen germination tests. The pollen phenotype of usp-1 was complemented by transformation of usp-1 with the AtUSP cDNA sequence. Surface and ultrastructural analyses of pollen from wild-type and usp mutants demonstrated that the mutation had no apparent effect on the outer wall (exine) but prevented the synthesis of the pectocellulosic inner wall (intine). Evidence presented here shows that AtUSP has a critical role in pollen development.
拟南芥UDP-糖焦磷酸化酶(AtUSP)是一种能合成核苷酸糖的广底物酶。AtUSP反应的产物可作为糖脂、糖蛋白以及包括果胶和半纤维素在内的细胞壁成分合成的前体。AtUSP在拟南芥中没有紧密同源物,其生物学功能尚未明确界定。我们鉴定出了AtUSP的两个T-DNA插入突变体品系,usp-1和usp-2。未鉴定出纯合个体,usp-1或usp-2杂合植株的后代在选择条件下呈现1:1的分离比。尽管AtUSP转录本水平和USP活性(UDP-GlcA→GlcA-1-P)均降低,但杂合植株在发育的各个阶段与野生型并无差异。正反交试验表明,分离畸变的来源是通过雄配子体的传递缺失。对四重奏背景下usp-1的花粉四分体分析显示,正常花粉粒与塌陷花粉粒的比例为2:2。通过亚历山大活力检测、DAPI染色和花粉萌发试验确定,塌陷的花粉粒没有活力。用AtUSP cDNA序列转化usp-1可互补usp-1的花粉表型。对野生型和usp突变体花粉的表面和超微结构分析表明,该突变对外壁(花粉外壁)没有明显影响,但阻止了果胶纤维素内壁(花粉内壁)的合成。本文提供的证据表明,AtUSP在花粉发育中起关键作用。